Sequences of DNA in the genes that are located between the EXONS. They are transcribed along with the exons but are removed from the primary gene transcript by RNA SPLICING to leave mature RNA. Some introns code for separate genes.
The ultimate exclusion of nonsense sequences or intervening sequences (introns) before the final RNA transcript is sent to the cytoplasm.
The sequence of PURINES and PYRIMIDINES in nucleic acids and polynucleotides. It is also called nucleotide sequence.
The parts of a transcript of a split GENE remaining after the INTRONS are removed. They are spliced together to become a MESSENGER RNA or other functional RNA.
Descriptions of specific amino acid, carbohydrate, or nucleotide sequences which have appeared in the published literature and/or are deposited in and maintained by databanks such as GENBANK, European Molecular Biology Laboratory (EMBL), National Biomedical Research Foundation (NBRF), or other sequence repositories.
Organelles in which the splicing and excision reactions that remove introns from precursor messenger RNA molecules occur. One component of a spliceosome is five small nuclear RNA molecules (U1, U2, U4, U5, U6) that, working in conjunction with proteins, help to fold pieces of RNA into the right shapes and later splice them into the message.
Nucleotide sequences located at the ends of EXONS and recognized in pre-messenger RNA by SPLICEOSOMES. They are joined during the RNA SPLICING reaction, forming the junctions between exons.
RNA transcripts of the DNA that are in some unfinished stage of post-transcriptional processing (RNA PROCESSING, POST-TRANSCRIPTIONAL) required for function. RNA precursors may undergo several steps of RNA SPLICING during which the phosphodiester bonds at exon-intron boundaries are cleaved and the introns are excised. Consequently a new bond is formed between the ends of the exons. Resulting mature RNAs can then be used; for example, mature mRNA (RNA, MESSENGER) is used as a template for protein production.
The process of cumulative change at the level of DNA; RNA; and PROTEINS, over successive generations.
The order of amino acids as they occur in a polypeptide chain. This is referred to as the primary structure of proteins. It is of fundamental importance in determining PROTEIN CONFORMATION.
The relationships of groups of organisms as reflected by their genetic makeup.
The insertion of recombinant DNA molecules from prokaryotic and/or eukaryotic sources into a replicating vehicle, such as a plasmid or virus vector, and the introduction of the resultant hybrid molecules into recipient cells without altering the viability of those cells.
The spatial arrangement of the atoms of a nucleic acid or polynucleotide that results in its characteristic 3-dimensional shape.
A process whereby multiple RNA transcripts are generated from a single gene. Alternative splicing involves the splicing together of other possible sets of EXONS during the processing of some, but not all, transcripts of the gene. Thus a particular exon may be connected to any one of several alternative exons to form a mature RNA. The alternative forms of mature MESSENGER RNA produce PROTEIN ISOFORMS in which one part of the isoforms is common while the other parts are different.
A category of nucleic acid sequences that function as units of heredity and which code for the basic instructions for the development, reproduction, and maintenance of organisms.
The sequential correspondence of nucleotides in one nucleic acid molecule with those of another nucleic acid molecule. Sequence homology is an indication of the genetic relatedness of different organisms and gene function.
The arrangement of two or more amino acid or base sequences from an organism or organisms in such a way as to align areas of the sequences sharing common properties. The degree of relatedness or homology between the sequences is predicted computationally or statistically based on weights assigned to the elements aligned between the sequences. This in turn can serve as a potential indicator of the genetic relatedness between the organisms.
RNA sequences that serve as templates for protein synthesis. Bacterial mRNAs are generally primary transcripts in that they do not require post-transcriptional processing. Eukaryotic mRNA is synthesized in the nucleus and must be exported to the cytoplasm for translation. Most eukaryotic mRNAs have a sequence of polyadenylic acid at the 3' end, referred to as the poly(A) tail. The function of this tail is not known for certain, but it may play a role in the export of mature mRNA from the nucleus as well as in helping stabilize some mRNA molecules by retarding their degradation in the cytoplasm.
Short chains of RNA (100-300 nucleotides long) that are abundant in the nucleus and usually complexed with proteins in snRNPs (RIBONUCLEOPROTEINS, SMALL NUCLEAR). Many function in the processing of messenger RNA precursors. Others, the snoRNAs (RNA, SMALL NUCLEOLAR), are involved with the processing of ribosomal RNA precursors.
A multistage process that includes cloning, physical mapping, subcloning, determination of the DNA SEQUENCE, and information analysis.
A sequence of amino acids in a polypeptide or of nucleotides in DNA or RNA that is similar across multiple species. A known set of conserved sequences is represented by a CONSENSUS SEQUENCE. AMINO ACID MOTIFS are often composed of conserved sequences.
RNA that has catalytic activity. The catalytic RNA sequence folds to form a complex surface that can function as an enzyme in reactions with itself and other molecules. It may function even in the absence of protein. There are numerous examples of RNA species that are acted upon by catalytic RNA, however the scope of this enzyme class is not limited to a particular type of substrate.
A species of fresh-water, flagellated EUKARYOTES in the phylum EUGLENIDA.
Ribonucleic acid in fungi having regulatory and catalytic roles as well as involvement in protein synthesis.
The biosynthesis of RNA carried out on a template of DNA. The biosynthesis of DNA from an RNA template is called REVERSE TRANSCRIPTION.
Use of restriction endonucleases to analyze and generate a physical map of genomes, genes, or other segments of DNA.
The degree of similarity between sequences of amino acids. This information is useful for the analyzing genetic relatedness of proteins and species.
A deoxyribonucleotide polymer that is the primary genetic material of all cells. Eukaryotic and prokaryotic organisms normally contain DNA in a double-stranded state, yet several important biological processes transiently involve single-stranded regions. DNA, which consists of a polysugar-phosphate backbone possessing projections of purines (adenine and guanine) and pyrimidines (thymine and cytosine), forms a double helix that is held together by hydrogen bonds between these purines and pyrimidines (adenine to thymine and guanine to cytosine).
A sequence of successive nucleotide triplets that are read as CODONS specifying AMINO ACIDS and begin with an INITIATOR CODON and end with a stop codon (CODON, TERMINATOR).
The process of cumulative change over successive generations through which organisms acquire their distinguishing morphological and physiological characteristics.
Theoretical representations that simulate the behavior or activity of genetic processes or phenomena. They include the use of mathematical equations, computers, and other electronic equipment.
Single-stranded complementary DNA synthesized from an RNA template by the action of RNA-dependent DNA polymerase. cDNA (i.e., complementary DNA, not circular DNA, not C-DNA) is used in a variety of molecular cloning experiments as well as serving as a specific hybridization probe.
The joining of RNA from two different genes. One type of trans-splicing is the "spliced leader" type (primarily found in protozoans such as trypanosomes and in lower invertebrates such as nematodes) which results in the addition of a capped, noncoding, spliced leader sequence to the 5' end of mRNAs. Another type of trans-splicing is the "discontinuous group II introns" type (found in plant/algal chloroplasts and plant mitochondria) which results in the joining of two independently transcribed coding sequences. Both are mechanistically similar to conventional nuclear pre-mRNA cis-splicing. Mammalian cells are also capable of trans-splicing.
The functional hereditary units of FUNGI.
Any method used for determining the location of and relative distances between genes on a chromosome.
The genetic complement of an organism, including all of its GENES, as represented in its DNA, or in some cases, its RNA.
The functional hereditary units of PLANTS.
A form of GENE LIBRARY containing the complete DNA sequences present in the genome of a given organism. It contrasts with a cDNA library which contains only sequences utilized in protein coding (lacking introns).
The restriction of a characteristic behavior, anatomical structure or physical system, such as immune response; metabolic response, or gene or gene variant to the members of one species. It refers to that property which differentiates one species from another but it is also used for phylogenetic levels higher or lower than the species.
In vitro method for producing large amounts of specific DNA or RNA fragments of defined length and sequence from small amounts of short oligonucleotide flanking sequences (primers). The essential steps include thermal denaturation of the double-stranded target molecules, annealing of the primers to their complementary sequences, and extension of the annealed primers by enzymatic synthesis with DNA polymerase. The reaction is efficient, specific, and extremely sensitive. Uses for the reaction include disease diagnosis, detection of difficult-to-isolate pathogens, mutation analysis, genetic testing, DNA sequencing, and analyzing evolutionary relationships.
A phylum of photosynthetic EUKARYOTA bearing double membrane-bound plastids containing chlorophyll a and b. They comprise the classical green algae, and represent over 7000 species that live in a variety of primarily aquatic habitats. Only about ten percent are marine species, most live in freshwater.
A method (first developed by E.M. Southern) for detection of DNA that has been electrophoretically separated and immobilized by blotting on nitrocellulose or other type of paper or nylon membrane followed by hybridization with labeled NUCLEIC ACID PROBES.
A class of EUKARYOTA (traditionally algae), characterized by biflagellated cells and found in both freshwater and marine environments. Pigmentation varies but only one CHLOROPLAST is present. Unique structures include a nucleomorph and ejectosomes.
The relative amounts of the PURINES and PYRIMIDINES in a nucleic acid.
A polynucleotide consisting essentially of chains with a repeating backbone of phosphate and ribose units to which nitrogenous bases are attached. RNA is unique among biological macromolecules in that it can encode genetic information, serve as an abundant structural component of cells, and also possesses catalytic activity. (Rieger et al., Glossary of Genetics: Classical and Molecular, 5th ed)
Highly conserved nuclear RNA-protein complexes that function in RNA processing in the nucleus, including pre-mRNA splicing and pre-mRNA 3'-end processing in the nucleoplasm, and pre-rRNA processing in the nucleolus (see RIBONUCLEOPROTEINS, SMALL NUCLEOLAR).
A phylum of fungi which have cross-walls or septa in the mycelium. The perfect state is characterized by the formation of a saclike cell (ascus) containing ascospores. Most pathogenic fungi with a known perfect state belong to this phylum.
Components of ribosomal RNA that undergo auto-catalyzed molecular rearrangements of their RNA sequence.
A nuclear RNA-protein complex that plays a role in RNA processing. In the nucleoplasm, the U2 snRNP along with other small nuclear ribonucleoproteins (U1, U4-U6, and U5) assemble into SPLICEOSOMES that remove introns from pre-mRNA by splicing. The U2 snRNA forms base pairs with conserved sequence motifs at the branch point, which associates with a heat- and RNAase-sensitive factor in an early step of splicing.
Elements that are transcribed into RNA, reverse-transcribed into DNA and then inserted into a new site in the genome. Long terminal repeats (LTRs) similar to those from retroviruses are contained in retrotransposons and retrovirus-like elements. Retroposons, such as LONG INTERSPERSED NUCLEOTIDE ELEMENTS and SHORT INTERSPERSED NUCLEOTIDE ELEMENTS do not contain LTRs.
Deoxyribonucleic acid that makes up the genetic material of fungi.
The most abundant form of RNA. Together with proteins, it forms the ribosomes, playing a structural role and also a role in ribosomal binding of mRNA and tRNAs. Individual chains are conventionally designated by their sedimentation coefficients. In eukaryotes, four large chains exist, synthesized in the nucleolus and constituting about 50% of the ribosome. (Dorland, 28th ed)
A genus of ciliate protozoa commonly used in genetic, cytological, and other research.
Genes bearing close resemblance to known genes at different loci, but rendered non-functional by additions or deletions in structure that prevent normal transcription or translation. When lacking introns and containing a poly-A segment near the downstream end (as a result of reverse copying from processed nuclear RNA into double-stranded DNA), they are called processed genes.
DNA sequences which are recognized (directly or indirectly) and bound by a DNA-dependent RNA polymerase during the initiation of transcription. Highly conserved sequences within the promoter include the Pribnow box in bacteria and the TATA BOX in eukaryotes.
The parts of the messenger RNA sequence that do not code for product, i.e. the 5' UNTRANSLATED REGIONS and 3' UNTRANSLATED REGIONS.
Any detectable and heritable change in the genetic material that causes a change in the GENOTYPE and which is transmitted to daughter cells and to succeeding generations.
Use for nucleic acid precursors in general or for which there is no specific heading.
A free-living soil amoeba pathogenic to humans and animals. It occurs also in water and sewage. The most commonly found species in man is NAEGLERIA FOWLERI which is the pathogen for primary amebic meningoencephalitis in primates.
A set of genes descended by duplication and variation from some ancestral gene. Such genes may be clustered together on the same chromosome or dispersed on different chromosomes. Examples of multigene families include those that encode the hemoglobins, immunoglobulins, histocompatibility antigens, actins, tubulins, keratins, collagens, heat shock proteins, salivary glue proteins, chorion proteins, cuticle proteins, yolk proteins, and phaseolins, as well as histones, ribosomal RNA, and transfer RNA genes. The latter three are examples of reiterated genes, where hundreds of identical genes are present in a tandem array. (King & Stanfield, A Dictionary of Genetics, 4th ed)
Enzymes that are part of the restriction-modification systems. They catalyze the endonucleolytic cleavage of DNA sequences which lack the species-specific methylation pattern in the host cell's DNA. Cleavage yields random or specific double-stranded fragments with terminal 5'-phosphates. The function of restriction enzymes is to destroy any foreign DNA that invades the host cell. Most have been studied in bacterial systems, but a few have been found in eukaryotic organisms. They are also used as tools for the systematic dissection and mapping of chromosomes, in the determination of base sequences of DNAs, and have made it possible to splice and recombine genes from one organism into the genome of another. EC 3.21.1.
Any of the DNA in between gene-coding DNA, including untranslated regions, 5' and 3' flanking regions, INTRONS, non-functional pseudogenes, and non-functional repetitive sequences. This DNA may or may not encode regulatory functions.
Animals having a vertebral column, members of the phylum Chordata, subphylum Craniata comprising mammals, birds, reptiles, amphibians, and fishes.
Sequences of DNA or RNA that occur in multiple copies. There are several types: INTERSPERSED REPETITIVE SEQUENCES are copies of transposable elements (DNA TRANSPOSABLE ELEMENTS or RETROELEMENTS) dispersed throughout the genome. TERMINAL REPEAT SEQUENCES flank both ends of another sequence, for example, the long terminal repeats (LTRs) on RETROVIRUSES. Variations may be direct repeats, those occurring in the same direction, or inverted repeats, those opposite to each other in direction. TANDEM REPEAT SEQUENCES are copies which lie adjacent to each other, direct or inverted (INVERTED REPEAT SEQUENCES).
Double-stranded DNA of MITOCHONDRIA. In eukaryotes, the mitochondrial GENOME is circular and codes for ribosomal RNAs, transfer RNAs, and about 10 proteins.
Short sequences (generally about 10 base pairs) of DNA that are complementary to sequences of messenger RNA and allow reverse transcriptases to start copying the adjacent sequences of mRNA. Primers are used extensively in genetic and molecular biology techniques.
Discrete segments of DNA which can excise and reintegrate to another site in the genome. Most are inactive, i.e., have not been found to exist outside the integrated state. DNA transposable elements include bacterial IS (insertion sequence) elements, Tn elements, the maize controlling elements Ac and Ds, Drosophila P, gypsy, and pogo elements, the human Tigger elements and the Tc and mariner elements which are found throughout the animal kingdom.
Databases containing information about NUCLEIC ACIDS such as BASE SEQUENCE; SNPS; NUCLEIC ACID CONFORMATION; and other properties. Information about the DNA fragments kept in a GENE LIBRARY or GENOMIC LIBRARY is often maintained in DNA databases.
A phylum of unicellular flagellates of ancient eukaryotic lineage with unclear taxonomy. They lack a CELL WALL but are covered by a proteinaceous flexible coat, the pellicle, that allows the cell to change shape. Historically some authorities considered them to be an order of protozoa and others classed them as ALGAE (some members have CHLOROPLASTS and some don't).
Cells of the higher organisms, containing a true nucleus bounded by a nuclear membrane.
Small nuclear RNAs that are involved in the processing of pre-ribosomal RNA in the nucleolus. Box C/D containing snoRNAs (U14, U15, U16, U20, U21 and U24-U63) direct site-specific methylation of various ribose moieties. Box H/ACA containing snoRNAs (E2, E3, U19, U23, and U64-U72) direct the conversion of specific uridines to pseudouridine. Site-specific cleavages resulting in the mature ribosomal RNAs are directed by snoRNAs U3, U8, U14, U22 and the snoRNA components of RNase MRP and RNase P.
Ribonucleic acid in plants having regulatory and catalytic roles as well as involvement in protein synthesis.
Plant cell inclusion bodies that contain the photosynthetic pigment CHLOROPHYLL, which is associated with the membrane of THYLAKOIDS. Chloroplasts occur in cells of leaves and young stems of plants. They are also found in some forms of PHYTOPLANKTON such as HAPTOPHYTA; DINOFLAGELLATES; DIATOMS; and CRYPTOPHYTA.
A set of three nucleotides in a protein coding sequence that specifies individual amino acids or a termination signal (CODON, TERMINATOR). Most codons are universal, but some organisms do not produce the transfer RNAs (RNA, TRANSFER) complementary to all codons. These codons are referred to as unassigned codons (CODONS, NONSENSE).
Deoxyribonucleic acid that makes up the genetic material of CHLOROPLASTS.
A kingdom of eukaryotic, heterotrophic organisms that live parasitically as saprobes, including MUSHROOMS; YEASTS; smuts, molds, etc. They reproduce either sexually or asexually, and have life cycles that range from simple to complex. Filamentous fungi, commonly known as molds, refer to those that grow as multicellular colonies.
Multicellular, eukaryotic life forms of kingdom Plantae (sensu lato), comprising the VIRIDIPLANTAE; RHODOPHYTA; and GLAUCOPHYTA; all of which acquired chloroplasts by direct endosymbiosis of CYANOBACTERIA. They are characterized by a mainly photosynthetic mode of nutrition; essentially unlimited growth at localized regions of cell divisions (MERISTEMS); cellulose within cells providing rigidity; the absence of organs of locomotion; absence of nervous and sensory systems; and an alternation of haploid and diploid generations.
The sequence at the 5' end of the messenger RNA that does not code for product. This sequence contains the ribosome binding site and other transcription and translation regulating sequences.
A species of the genus SACCHAROMYCES, family Saccharomycetaceae, order Saccharomycetales, known as "baker's" or "brewer's" yeast. The dried form is used as a dietary supplement.
Post-transcriptional biological modification of messenger, transfer, or ribosomal RNAs or their precursors. It includes cleavage, methylation, thiolation, isopentenylation, pseudouridine formation, conformational changes, and association with ribosomal protein.
Proteins that bind to RNA molecules. Included here are RIBONUCLEOPROTEINS and other proteins whose function is to bind specifically to RNA.
Enzymes that catalyze the hydrolysis of the internal bonds and thereby the formation of polynucleotides or oligonucleotides from ribo- or deoxyribonucleotide chains. EC 3.1.-.
A plant division. They are simple plants that lack vascular tissue and possess rudimentary rootlike organs (rhizoids). Like MOSSES, liverworts have alternation of generations between haploid gamete-bearing forms (gametophytes) and diploid spore-bearing forms (sporophytes).
The functional hereditary units of protozoa.
Widely used technique which exploits the ability of complementary sequences in single-stranded DNAs or RNAs to pair with each other to form a double helix. Hybridization can take place between two complimentary DNA sequences, between a single-stranded DNA and a complementary RNA, or between two RNA sequences. The technique is used to detect and isolate specific sequences, measure homology, or define other characteristics of one or both strands. (Kendrew, Encyclopedia of Molecular Biology, 1994, p503)
A species of fruit fly much used in genetics because of the large size of its chromosomes.
Partial cDNA (DNA, COMPLEMENTARY) sequences that are unique to the cDNAs from which they were derived.
Ribonucleic acid in archaea having regulatory and catalytic roles as well as involvement in protein synthesis.
A plant genus of the family BRASSICACEAE that contains ARABIDOPSIS PROTEINS and MADS DOMAIN PROTEINS. The species A. thaliana is used for experiments in classical plant genetics as well as molecular genetic studies in plant physiology, biochemistry, and development.
The internal fragments of precursor proteins (INternal proTEINS) that are autocatalytically removed by PROTEIN SPLICING. The flanking fragments (EXTEINS) are ligated forming mature proteins. The nucleic acid sequences coding for inteins are considered to be MOBILE GENETIC ELEMENTS. Inteins are composed of self-splicing domains and an endonuclease domain which plays a role in the spread of the intein's genomic sequence. Mini-inteins are composed of the self-splicing domains only.
A phylum of fungi that produce their sexual spores (basidiospores) on the outside of the basidium. It includes forms commonly known as mushrooms, boletes, puffballs, earthstars, stinkhorns, bird's-nest fungi, jelly fungi, bracket or shelf fungi, and rust and smut fungi.
Proteins found in ribosomes. They are believed to have a catalytic function in reconstituting biologically active ribosomal subunits.
A field of biology concerned with the development of techniques for the collection and manipulation of biological data, and the use of such data to make biological discoveries or predictions. This field encompasses all computational methods and theories for solving biological problems including manipulation of models and datasets.
An order of CRENARCHAEOTA comprised of rod, disc, or spherical shaped, nonseptate, anaerobic, extreme thermophiles and found in solfataric hot waters, mud holes, and superheated submarine environments.
Cytochromes of the b group that have alpha-band absorption of 563-564 nm. They occur as subunits in MITOCHONDRIAL ELECTRON TRANSPORT COMPLEX III.
The genetic complement of MITOCHONDRIA as represented in their DNA.
A large collection of DNA fragments cloned (CLONING, MOLECULAR) from a given organism, tissue, organ, or cell type. It may contain complete genomic sequences (GENOMIC LIBRARY) or complementary DNA sequences, the latter being formed from messenger RNA and lacking intron sequences.
Genotypic differences observed among individuals in a population.
Detection of RNA that has been electrophoretically separated and immobilized by blotting on nitrocellulose or other type of paper or nylon membrane followed by hybridization with labeled NUCLEIC ACID PROBES.
The genetic complement of a plant (PLANTS) as represented in its DNA.
Deoxyribonucleic acid that makes up the genetic material of plants.
A theoretical representative nucleotide or amino acid sequence in which each nucleotide or amino acid is the one which occurs most frequently at that site in the different sequences which occur in nature. The phrase also refers to an actual sequence which approximates the theoretical consensus. A known CONSERVED SEQUENCE set is represented by a consensus sequence. Commonly observed supersecondary protein structures (AMINO ACID MOTIFS) are often formed by conserved sequences.
A genus of EUKARYOTES, in the phylum EUGLENIDA, found mostly in stagnant water. Characteristics include a pellicle usually marked by spiral or longitudinal striations.

In vivo expression of the nucleolar group I intron-encoded I-dirI homing endonuclease involves the removal of a spliceosomal intron. (1/9869)

The Didymium iridis DiSSU1 intron is located in the nuclear SSU rDNA and has an unusual twin-ribozyme organization. One of the ribozymes (DiGIR2) catalyses intron excision and exon ligation. The other ribozyme (DiGIR1), which along with the endonuclease-encoding I-DirI open reading frame (ORF) is inserted in DiGIR2, carries out hydrolysis at internal processing sites (IPS1 and IPS2) located at its 3' end. Examination of the in vivo expression of DiSSU1 shows that after excision, DiSSU1 is matured further into the I-DirI mRNA by internal DiGIR1-catalysed cleavage upstream of the ORF 5' end, as well as truncation and polyadenylation downstream of the ORF 3' end. A spliceosomal intron, the first to be reported within a group I intron and the rDNA, is removed before the I-DirI mRNA associates with the polysomes. Taken together, our results imply that DiSSU1 uses a unique combination of intron-supplied ribozyme activity and adaptation to the general RNA polymerase II pathway of mRNA expression to allow a protein to be produced from the RNA polymerase I-transcribed rDNA.  (+info)

Tight binding of the 5' exon to domain I of a group II self-splicing intron requires completion of the intron active site. (2/9869)

Group II self-splicing requires the 5' exon to form base pairs with two stretches of intronic sequence (EBS1 and EBS2) which also bind the DNA target during retrotransposition of the intron. We have used dimethyl sulfate modification of bases to obtain footprints of the 5' exon on intron Pl.LSU/2 from the mitochondrion of the alga Pylaiella littoralis, as well as on truncated intron derivatives. Aside from the EBS sites, which are part of the same subdomain (ID) of ribozyme secondary structure, three distant adenines become either less or more sensitive to modification in the presence of the exon. Unexpectedly, one of these adenines in subdomain IC1 is footprinted only in the presence of the distal helix of domain V, which is involved in catalysis. While the loss of that footprint is accompanied by a 100-fold decrease in the affinity for the exon, both protection from modification and efficient binding can be restored by a separate domain V transcript, whose binding results in its own, concise footprint on domains I and III. Possible biological implications of the need for the group II active site to be complete in order to observe high-affinity binding of the 5' exon to domain I are discussed.  (+info)

A premature termination codon interferes with the nuclear function of an exon splicing enhancer in an open reading frame-dependent manner. (3/9869)

Premature translation termination codon (PTC)-mediated effects on nuclear RNA processing have been shown to be associated with a number of human genetic diseases; however, how these PTCs mediate such effects in the nucleus is unclear. A PTC at nucleotide (nt) 2018 that lies adjacent to the 5' element of a bipartite exon splicing enhancer within the NS2-specific exon of minute virus of mice P4 promoter-generated pre-mRNA caused a decrease in the accumulated levels of P4-generated R2 mRNA relative to P4-generated R1 mRNA, although the total accumulated levels of P4 product remained the same. This effect was seen in nuclear RNA and was independent of RNA stability. The 5' and 3' elements of the bipartite NS2-specific exon enhancer are redundant in function, and when the 2018 PTC was combined with a deletion of the 3' enhancer element, the exon was skipped in the majority of the viral P4-generated product. Such exon skipping in response to a PTC, but not a missense mutation at nt 2018, could be suppressed by frame shift mutations in either exon of NS2 which reopened the NS2 open reading frame, as well as by improvement of the upstream intron 3' splice site. These results suggest that a PTC can interfere with the function of an exon splicing enhancer in an open reading frame-dependent manner and that the PTC is recognized in the nucleus.  (+info)

Alterations in the conserved SL1 trans-spliced leader of Caenorhabditis elegans demonstrate flexibility in length and sequence requirements in vivo. (4/9869)

Approximately 70% of mRNAs in Caenorhabditis elegans are trans spliced to conserved 21- to 23-nucleotide leader RNAs. While the function of SL1, the major C. elegans trans-spliced leader, is unknown, SL1 RNA, which contains this leader, is essential for embryogenesis. Efforts to characterize in vivo requirements of the SL1 leader sequence have been severely constrained by the essential role of the corresponding DNA sequences in SL1 RNA transcription. We devised a heterologous expression system that circumvents this problem, making it possible to probe the length and sequence requirements of the SL1 leader without interfering with its transcription. We report that expression of SL1 from a U2 snRNA promoter rescues mutants lacking the SL1-encoding genes and that the essential embryonic function of SL1 is retained when approximately one-third of the leader sequence and/or the length of the leader is significantly altered. In contrast, although all mutant SL1 RNAs were well expressed, more severe alterations eliminate this essential embryonic function. The one non-rescuing mutant leader tested was never detected on messages, demonstrating that part of the leader sequence is essential for trans splicing in vivo. Thus, in spite of the high degree of SL1 sequence conservation, its length, primary sequence, and composition are not critical parameters of its essential embryonic function. However, particular nucleotides in the leader are essential for the in vivo function of the SL1 RNA, perhaps for its assembly into a functional snRNP or for the trans-splicing reaction.  (+info)

Promoter and exon-intron structure of the protein kinase C gene from the marine sponge Geodia cydonium: evolutionary considerations and promoter activity. (5/9869)

We report the gene structure of a key signaling molecule from a marine sponge, Geodia cydonium. The selected gene, which codes for a classical protein kinase C (cPKC), comprises 13 exons and 12 introns; the introns are, in contrast to those found in cPKC from higher Metazoa, small in size ranging from 93 nt to 359 nt. The complete gene has a length of 4229 nt and contains exons which encode the characteristic putative regulatory and catalytic domains of metazoan cPKCs. While in the regulatory domain only one intron is in phase 0, in the catalytic domain most introns are phase 0 introns, suggesting that the latter only rarely undergo module duplication. The 5'-flanking sequence of the sponge cPKC gene contains a TATA-box like motif which is located 35-26 nt upstream from the start of the longest sequenced cDNA. This 5'-flanking sequence was analyzed for promoter activity. The longest fragment (538 nt) was able to drive the expression of luciferase in transient transfections of NIH 3T3 fibroblasts; the strong activity of the sponge promoter was found to be half the one displayed by the SV40 reference promoter. Deletion analysis demonstrates that the AP4 site and the GC box which is most adjacent to the TATA box are the crucial elements for maximal promoter activity. The activity of the promoter is not changed in 3T3 cells which are kept serum starved or in the presence of a phorbol ester. In conclusion, these data present the phylogenetically oldest cPKC gene which contains in the 5'-flanking region a promoter functional in the heterologous mammalian cell system.  (+info)

Interleukin-18 binding protein: a novel modulator of the Th1 cytokine response. (6/9869)

An interleukin-18 binding protein (IL-18BP) was purified from urine by chromatography on IL-18 beads, sequenced, cloned, and expressed in COS7 cells. IL-18BP abolished IL-18 induction of interferon-gamma (IFNgamma), IL-8, and activation of NF-kappaB in vitro. Administration of IL-18BP to mice abrogated circulating IFNgamma following LPS. Thus, IL-18BP functions as an inhibitor of the early Th1 cytokine response. IL-18BP is constitutively expressed in the spleen, belongs to the immunoglobulin superfamily, and has limited homology to the IL-1 type II receptor. Its gene was localized on human chromosome 11q13, and no exon coding for a transmembrane domain was found in an 8.3 kb genomic sequence. Several Poxviruses encode putative proteins highly homologous to IL-18BP, suggesting that viral products may attenuate IL-18 and interfere with the cytotoxic T cell response.  (+info)

The stability and fate of a spliced intron from vertebrate cells. (7/9869)

Introns constitute most of the length of typical pre-mRNAs in vertebrate cells. Thus, the turnover rate of introns may significantly influence the availability of ribonucleotides and splicing factors for further rounds of transcription and RNA splicing, respectively. Given the importance of intron turnover, it is surprising that there have been no reports on the half-life of introns from higher eukaryotic cells. Here, we determined the stability of IVS1Cbeta1, the first intron from the constant region of the mouse T-cell receptor-beta, (TCR-beta) gene. Using a tetracycline (tet)-regulated promoter, we demonstrate that spliced IVS1Cbeta1 and its pre-mRNA had half-lives of 6.0+/-1.4 min and 3.7+/-1.0 min, respectively. We also examined the half-lives of these transcripts by using actinomycin D (Act.D). Act.D significantly stabilized IVS1Cbeta1 and its pre-mRNA, suggesting that Act.D not only blocks transcription but exerts rapid and direct posttranscriptional effects in the nucleus. We observed that in vivo spliced IVS1Cbeta1 accumulated predominantly as lariat molecules that use a consensus branchpoint nucleotide. The accumulation of IVS1Cbeta1 as a lariat did not result from an intrinsic inability to be debranched, as it could be debranched in vitro, albeit somewhat less efficiently than an adenovirus intron. Subcellular-fractionation and sucrose-gradient analyses showed that most spliced IVS1Cbeta1 lariats cofractionated with pre-mRNA, but not always with mRNA in the nucleus. Some IVS1Cbeta1 also appeared to be selectively exported to the cytoplasm, whereas TCR-beta pre-mRNA remained in the nucleus. This study constitutes the first detailed analysis of the stability and fate of a spliced nuclear intron in vivo.  (+info)

Genome-wide bioinformatic and molecular analysis of introns in Saccharomyces cerevisiae. (8/9869)

Introns have typically been discovered in an ad hoc fashion: introns are found as a gene is characterized for other reasons. As complete eukaryotic genome sequences become available, better methods for predicting RNA processing signals in raw sequence will be necessary in order to discover genes and predict their expression. Here we present a catalog of 228 yeast introns, arrived at through a combination of bioinformatic and molecular analysis. Introns annotated in the Saccharomyces Genome Database (SGD) were evaluated, questionable introns were removed after failing a test for splicing in vivo, and known introns absent from the SGD annotation were added. A novel branchpoint sequence, AAUUAAC, was identified within an annotated intron that lacks a six-of-seven match to the highly conserved branchpoint consensus UACUAAC. Analysis of the database corroborates many conclusions about pre-mRNA substrate requirements for splicing derived from experimental studies, but indicates that splicing in yeast may not be as rigidly determined by splice-site conservation as had previously been thought. Using this database and a molecular technique that directly displays the lariat intron products of spliced transcripts (intron display), we suggest that the current set of 228 introns is still not complete, and that additional intron-containing genes remain to be discovered in yeast. The database can be accessed at http://www.cse.ucsc.edu/research/compbi o/yeast_introns.html.  (+info)

While the role of group I and group II intron-encoded proteins in homing has been well defined, the function of these proteins in intron dissemination to new sites remains the subject of intense study. These mobile introns, their intron-encoded proteins, and the mechanisms by which mobility occurs are the subject of this chapter. Although transition metals are not required for colicin DNase activity, it is likely that they play a stabilizing role related to the membrane translocation that must occur for colicins biological function. These data lend credence to the idea that the HNH domain, like the GIY-YIG domain, is an endonu clease cassette that can become associated with other protein domains to form multifunctional proteins. The open reading frames (ORFs) specifying group II intron-encoded proteins, when present, are located in the loop region of the structural domain IV, with most of the coding sequence outside the intron catalytic core. Of the three activities of the group II intron-encoded
Group II Self-Splicing Introns. -pre-rRNA of fungal and plant mitochondria -majority of chloroplast introns -several classes -require Mg 2+ -no cofactor. Domain Structure of a Group II Intron. A. 5 exon. 3 exon. Chemistry of Group II Self-Splicing. 1st step. 2nd step. lariat. Slideshow 3387240 by guang
Structure and Conformational Dynamics of the Domain 5 RNA Hairpin of a Bacterial Group II Intron Revealed by Solution Nuclear Magnetic Resonance and Molecular Dynamics ...
TY - JOUR. T1 - Intron size, abundance, and distribution within untranslated regions of genes. AU - Hong, Xin. AU - Scofield, Douglas G.. AU - Lynch, Michael. PY - 2006/12. Y1 - 2006/12. N2 - Most research concerning the evolution of introns has largely considered introns within coding sequences (CDSs), without regard for introns located within untranslated regions (UTRs) of genes. Here, we directly determined intron size, abundance, and distribution in UTRs of genes using full-length cDNA libraries and complete genome sequences for four species, Arabidopsis thaliana, Drosophila melanogaster, human, and mouse. Overall intron occupancy (introns/exon kbp) is lower in 5′ UTRs than CDSs, but intron density (intron occupancy in regions containing introns) tends to be higher in 5′ UTRs than in CDSs. Introns in 5′ UTRs are roughly twice as large as introns in CDSs, and there is a sharp drop in intron size at the 5′ UTR-CDS boundary. We propose a mechanistic explanation for the existence of ...
Exon shuffling was first introduced in 1978 when Walter Gilbert discovered that the existence of introns could play a major role in the evolution of proteins. It was noted that recombination within introns could help assort exons independently and that repetitive segments in the middle of introns could create hotspots for recombination to shuffle the exonic sequences. However, the presence of these introns in eukaryotes and absence in prokaryotes created a debate about the time in which these introns appeared. Two theories arose: the introns early theory and the introns late theory. Supporters of the introns early theory believed that introns and RNA splicing were the relics of the RNA world and therefore both prokaryotes and eukaryotes had introns in the beginning. However, prokaryotes eliminated their introns in order to obtain a higher efficiency, while eukaryotes retained the introns and the genetic plasticity of the ancestors. On the other hand, supporters of the introns late theory ...
The object isnt able to load since the IDs are different. Same is the case with exons and transcripts ids. Upon looking into the .ctab files, the exons, introns, transcripts differ across Control- Sample. But are same across the 3 controls. And they are same across the 5 samples. It is like so- Controls: exon 442247, introns 366654, transcripts 181466. Samples: exon 686514, introns 416565, transcripts 247538. The exons, introns, transcripts differ only between the two conditions. Hence, I am not able to progress from here. Can anyone please help me with as to why this is occuring? Why would the exons, introns, transcripts id be different for control & sample, since both control and sample RNA are collected from human patients. Please add a note on how I can solve this issue.. Any help is much appreciated.. ...
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about Alamut. We are very pleased with Alamut since it conveniently streamlines post-sequencing analyses of detected variants. We value the programme user friendliness and its all-in one approach to variant analysis.. PROF. MILAN MACEK Jr. M.D. Ph.D ...
The objective of this study was primarily to determine the structure and biochemical characteristics of the NmeGp1Sd in order to gain a deeper insight into the evolution of metazoan Nme proteins and their functions.. Sponge Group I Nme genes are intron-rich and these introns are relatively short. The same has been found for introns in several other sponge genes [42, 43] and recently in A. queenslandica genome where median intron size is 80 bp [32]. The fourth intron (Figure 1) is likely the most ancient because it is also found in a choanoflagellate Group I Nme homolog. We conclude that the ancestral metazoan Group I Nme gene was intron-rich and probably had all four introns that are still present in most extant basal metazoan homologs. The ancestral gene structure is also well preserved in vertebrate homologs with three out of four introns present. D. melanogaster has only one of the ancestral introns and C. elegans lost all ancestral introns and gained two new ones which likely reflect ...
Introns may be lost or gained over evolutionary time, as shown by many comparative studies of orthologous genes. Subsequent analyses have identified thousands of examples of intron loss and gain events, and it has been proposed that the emergence of eukaryotes, or the initial stages of eukaryotic evolution, involved an intron invasion.[32] Two definitive mechanisms of intron loss, Reverse Transcriptase-Mediated Intron Loss (RTMIL) and genomic deletions, have been identified, and are known to occur.[33] The definitive mechanisms of intron gain, however, remain elusive and controversial. At least seven mechanisms of intron gain have been reported thus far: Intron Transposition, Transposon Insertion, Tandem Genomic Duplication, Intron Transfer, Intron Gain during Double-Strand Break Repair (DSBR), Insertion of a Group II Intron, and Intronization. In theory it should be easiest to deduce the origin of recently gained introns due to the lack of host-induced mutations, yet even introns gained ...
Many functional RNAs are required to fold into specific three-dimensional structures. A fundamental property of RNA is that its secondary structure and even some tertiary contacts are highly stable, which gives rise to independent modular RNA motifs and makes RNAs prone to adopting misfolded intermediates. Consequently, in addition to stabilizing the native structure relative to the unfolded species (defined here as stability), RNAs are faced with the challenge of stabilizing the native structure relative to alternative structures (defined as structural specificity). How RNAs have evolved to overcome these challenges is incompletely understood. Self-splicing group I introns have been used to study RNA structure and folding for decades. Among them, the Tetrahymena intron was the first discovered and has been studied extensively. In this work, we found that a version of the intron that was generated by in vitro selection for enhanced stability also displayed enhanced specificity against a stable ...
Group II introns are large metallo-ribozymes that use divalent metal ions in folding and catalysis. The 3-terminal domain 6 contains a conserved adenosine whose 2-OH acts as the nucleophile in the first splicing step. In the hierarchy of folding, D6 binds last into the active site. In order to investigate and understand the folding process to the catalytically active intron structure, it is important to know the individual binding affinities of Mg2+ ions to D6. We recently studied the solution structure of a 27 nucleotide long domain 6 (D6-27) from the mitochondrial yeast group II intron Sc.ai5, identifying also five Mg2+ binding sites including the one at the 5-terminal phosphate residues. Mg2+ coordination to the 5-terminal di- and triphosphate groups is strongest (e.g., log KA,TP = 4.55 ± 0.10) and could be evaluated here in detail for the first time. The other four binding sites within D6-27 are filled simultaneously (e.g., log KA,BR = 2.38 ± 0.06) and thus compete for the free Mg2+ ...
The exon/intron organisation of homologous nuclear genes was compared in several yeast species. CLUSTALX multiple alignments were performed to verify the degree of conservation of the homologues and to reconstruct a virtual (scaffold) gene, exhibiting the probable ancestral intron arrangement. Intron position was defined at the nucleotide level making it possible to determine whether the intron is at an identical position (same codon and same phase) or not in the homologues.. In the cases herein illustrated, some intron positions were found divergent in homologues sharing a high degree of sequence conservation, suggesting that these positions may result either from intron sliding or intron gain events [Bon et al., 2003]. Intron sliding is defined as the relocation of a pre-existing intron over short distances in the course of gene evolution [Rogozin et al., 2000, Trends Genet., 16, 430-432]. Although it is now admitted that intron sliding by one or two bases is a real phenomenon, it remains ...
This site contains information about the spliceosomal introns of the yeast Saccharomyces cerevisiae. Introns present special problems for the annotation of eukaryotic genomes. Splice sites are information-poor, and their recognition by the splicing apparatus is highly context-dependent and regulated, making identification by computational gene prediction programs a challenge. At present we do not understand splice site context well enough to predict which potential splice sites will be used, and thus how the genomic sequences will be expressed. Understanding the how and why of introns will require genome level information about splicing. One element of this will involve understanding splicing patterns and how they are regulated globally. Another element will involve understanding how splicing patterns change during evolution. To begin we study yeast, since it has the simplest known eukaryotic genome. In these pages we have listed known spliceosomal introns in the yeast genome and documented the ...
Recording during rehearsal, december 2018 Reboot by de Introns Recordings 2016 with former member Theo on the drums. de Introns by de Introns
The wide, but scattered distribution of group I introns in nature is a result of two processes; the vertical inheritance of introns with or without losses, and the occasional transfer of introns across species barriers. Reversal of the group I intron
Most metazoan genes have multiple exons that must be carefully excised (from the pre-mRNA) and then ligated (to form the mRNA). This RNA splicing occurs in the nucleus, and upon its completion the mRNA is exported to the cytoplasm for translation. Exon definition complexes and spliceosomes begin to assemble during transcription. Some of these complexes interact with RNAP IIs CTD, and some introns are thus excised before transcription has even terminated.. There is no apparent order in which introns get spliced). Introns do no excise in any particular order, and active transcription (or its termination) is not needed for splicing to occur. However, the rate of transcription elongation through an intron can strongly affect what splice sites are chosen and thus indirectly couple transcription and splicing. Exon definition complexes and spliceosomes begin assembling during RNA synthesis; interaction with RNAP IIs CTD leads to excision of some introns before transcription has even ...
Isolation and Characterization of Functional Tripartite Group II Introns Using a Tn5-Based Genetic Screen. . Biblioteca virtual para leer y descargar libros, documentos, trabajos y tesis universitarias en PDF. Material universiario, documentación y tareas realizadas por universitarios en nuestra biblioteca. Para descargar gratis y para leer online.
Group II Introns: Structure, Function, and Catalysis - CHEMICAL BIOLOGY - reflects the multidimensional character of chemical biology, focusing in particular on the fundamental science of biological structures and systems, the use of chemical and biological techniques to elucidate
We read with great interest the recent paper by Beer and Sahin-Tóth1 addressing the missing heritability observed in approximately 60% of German cases of chronic pancreatitis.2 These authors opined that discovery studies tend to focus on exons and exon-intron boundaries and may thus miss many intronic variants.1 This premise seems eminently reasonable, given the generally much larger size of intronic sequences as compared with the coding sequences of protein-coding genes. However, there is a trade-off here. On the one hand, larger sequence size means larger target size for mutation, and hence the greater the number of mutations that could be missed if intronic sequences were not screened. On the other hand, to be of pathological significance, an intronic mutation must either create a new functional splicing donor or acceptor site or alternatively impact a functional sequence motif responsible for regulating splicing (eg, an intronic splicing enhancer), which depends upon many additional ...
There are many unanswered questions about introns. It is unclear whether introns serve some specific function, or whether they are selfish DNA which reproduces itself as a parasite.[5] Recent studies of entire eukaryotic genomes have now shown that the lengths and density (introns/gene) of introns varies considerably between related species. There are four or five different kinds of intron. Some introns represent mobile genetic elements (transposons). Alternative splicing of introns within a gene allows a variety of protein isoforms from a single gene. Thus multiple related proteins can be generated from a single gene and a single precursor mRNA transcript. The control of alternative RNA splicing is performed by complex network of signalling molecules. In humans, ~95% of genes with more than one exon are alternatively spliced.[6] ...
For each BAM, we use samtools to retrieve the reads in the region(s)) of interest. The reads are then filtered with samjs (https://github.com/lindenb/jvarkit/wiki/SamJS) to only keep the reads carrying an intron-exon junction at the desired location(s). Basically, the javascript-based filter loops over the CIGAR string of the read, computes the genomic interval skipped when the cigar operator is a deletion or a skipped region/intron. The read is printed if it describes the new intron-exon junction ...
We compared the expression patterns and functional annotations of genes with and without 5UIs. We found that the most highly expressed genes reveal a strong enrichment for having short 5UIs as opposed to having either no 5UIs or longer 5UIs. This effect was specific to genes with the highest expression levels and no relationship between length and expression level was observed for genes with intermediate or long introns (Figure2d). These results are contrary to the energetic cost model [23], which predicts that genes with no 5UIs will be more highly represented among those with the highest expression levels. Because expression reflects both production and degradation rates of mRNAs, our results suggest that short 5UIs tend to either enhance transcription or stabilize mature mRNAs.. The prevalence and the significance of these intron-dependent mechanisms of transcriptional enhancement at a genome-wide level are poorly understood in mammalian systems. There are a few examples in mammals of ...
An intron is any nucleotide sequence within a gene that is removed by RNA splicing to generate the final mature RNA product of a gene.[1][2]The term intron refers to both the DNA sequence within a gene, and the corresponding sequence in RNA transcripts.[3] Sequences that are joined together in the final mature RNA after RNA splicing are exons. Introns are found in the genes of most organisms and many viruses, and can be located in a wide range of genes, including those that generate proteins, ribosomal RNA (rRNA), and transfer RNA (tRNA). When proteins are generated from intron-containing genes, RNA splicing takes place as part of the RNA processing pathway that followstranscription and precedes translation ...
An intron is any nucleotide sequence within a gene that is removed by RNA splicing to generate the final mature RNA product of a gene.[1][2]The term intron refers to both the DNA sequence within a gene, and the corresponding sequence in RNA transcripts.[3] Sequences that are joined together in the final mature RNA after RNA splicing are exons. Introns are found in the genes of most organisms and many viruses, and can be located in a wide range of genes, including those that generate proteins, ribosomal RNA (rRNA), and transfer RNA (tRNA). When proteins are generated from intron-containing genes, RNA splicing takes place as part of the RNA processing pathway that followstranscription and precedes translation ...
[Ive combined all the previous intron entries together to make it easier to read. However, did not have the time to thoroughly edit, so some parts might seem a little repetitive.] Since I will be discussing introns, let me begin with a few points of clarification. First, I will be focusing on introns found in…
Comparison of gene expression from transgenes and endogenous genes with or without introns reveals a time-regulating role of introns in natural biological systems.
The sections of m RNA which do not code for translation of a polypeptide are called introns.. As the m RNA readies itself to leave the nucleus, enzymes cut out and remove the introns.. …. These are cut out of the mRNA and kept in the nucleus.. Exons: Sections of mRNA containing the code to synthesize a protein... ...
a Overview of MASP1 mutations. Exons and introns are indicated by circles with numbers and thin lines, respectively. The localization of mutations identified in
Then there are introns, which are often considered DNA spacers with a possible error-checking function, inside the DNA strand. Introns do not code for proteins. Some species have a lot of introns in total DNA. Exons are what is leftover in the DNA strand when the introns have been peeled off. Exons can be less than 60% of the total DNA. It is likely the introns are for a reason, but they do represent a change that is kind of like fiber filling, sort of a do-nothing or copy-proofing addition ...
Usually the primary challenge that follows the sequencing of anything from a small segment of DNA to a complete genome is to establish where the location functional elements such as: genes (intron/exon boundaries) promoters, terminators etc DNA sequences that may potentially encode proteins are called Open Reading Frames (ORFs) The situation in prokaryotes is relatively straightforward since scarcely any eubacterial and archaeal genes contain introns
Phylogenetic analysis of 71 group II intron ORFs. A maximum likelihood analysis of the amino acid sequence for 71 ORFs suggests the cox1 ORF718 of the marine ce
Lateral transfer of an intron to a homologous allele that lacks the intron, mediated by a site-specific endonuclease encoded within the mobile intron.
Berget, S.M., Sharp, P.A. (1977) A spliced sequence at the 5′-terminus of adenovirus late mRNA. Brookhaven Symp Biol, 29:332-44.. Berk, A.J., Sharp, P.A. (1977) Sizing and mapping of early adenovirus mRNAs by gel electrophoresis of S1 endonuclease-digested hybrids. Cell 12(3): 721-32.. Chow, L.T., Roberts, J.M., Lewis, J.B., Broker, T.R. (1977) A map of cytoplasmic RNA transcripts from lytic adenovirus type 2, determined by electron microscopy of RNA:DNA hybrids. Cell, 11(4): 819-36.. Gibbs, W.W. (2003) The unseen genome: gems among the junk. Scientific American 289(5):26-33.. Hooks, K. B., Delneri, D. & Grifths-Jones, S. (2014) Intron evolution in Saccharomycetaceae. Genome Biol. Evol. 6, 2543-2556.. Kabat, J.L., Barberan-Soler, S., McKenna, P., Clawson, H., Farrer, T., and Zahler, A.M. (2006) Intronic Alternative Splicing Regulators Identified by Comparative Genomics in Nematodes. PLoS Computational Biology 2(7):734-747.. Kiss, T. and Filipowicz, W. (1995) Genes and Development ...
The conventional model for splicing involves excision of each intron in one piece; we demonstrate this inaccurately describes splicing in many human genes. First, after switching on transcription of SAMD4A, a gene with a 134 kb-long first intron, splicing joins the 3 end of exon 1 to successive points within intron 1 well before the acceptor site at exon 2 is made. Second, genome-wide analysis shows that |60% of active genes yield products generated by such intermediate intron splicing. These products are present at ∼15% the levels of primary transcripts, are encoded by conserved sequences similar to those found at canonical acceptors, and marked by distinctive structural and epigenetic features. Finally, using targeted genome editing, we demonstrate that inhibiting the formation of these splicing intermediates affects efficient exon-exon splicing. These findings greatly expand the functional and regulatory complexity of the human transcriptome.
Dear fly people: I have been trying to find some references about the cases in Drosophila in which one genes coding sequence (exon) resides in another genes intron region. I heard of examples, but would like to have a few papers to look at. Could someone give me a quick hand? Thanks a lot ...
All ESTs in GenBank on the date of the track data freeze for the given organism are used - none are discarded. When two ESTs have identical sequences, both are retained because this can be significant corroboration of a splice site.. ESTs are aligned against the genome using the Blat program. When a single EST aligns in multiple places, the alignment having the highest base identity is found. Only alignments that have a base identity level within a selected percentage of the best are kept. Alignments must also have a minimum base identity to be kept. For more information on the selection criteria specific to each organism, consult the description page accompanying the EST track for that organism.. The maximum intron length allowed by Blat is 500,000 bases, which may eliminate some ESTs with very long introns that might otherwise align. If an EST aligns non-contiguously (i.e. an intron has been spliced out), it is also a candidate for the Spliced EST track, provided it meets various quality ...
All ESTs in GenBank on the date of the track data freeze for the given organism are used - none are discarded. When two ESTs have identical sequences, both are retained because this can be significant corroboration of a splice site.. ESTs are aligned against the genome using the Blat program. When a single EST aligns in multiple places, the alignment having the highest base identity is found. Only alignments that have a base identity level within a selected percentage of the best are kept. Alignments must also have a minimum base identity to be kept. For more information on the selection criteria specific to each organism, consult the description page accompanying the EST track for that organism.. The maximum intron length allowed by Blat is 500,000 bases, which may eliminate some ESTs with very long introns that might otherwise align. If an EST aligns non-contiguously (i.e. an intron has been spliced out), it is also a candidate for the Spliced EST track, provided it meets various quality ...
To test for conservation, researchers need to find matching stretches in the two species. This is relatively easy for stretches that code for proteins, where scientists long ago learned the meaning of the sequence. For noncoding regions, however, the comparison is often ambiguous. Even within a gene, stretches of DNA that code for pieces of the target protein are usually interspersed with much larger noncoding stretches, called introns, that are removed from the RNA working copy of the DNA before the protein is made.. Previously, researchers assumed that mutations in the middle of introns do not affect the final protein, so they simply accumulate. In the new study, however, the researchers found signs that evolution rejects some types of mutations even in these regions of the genome. Although the selection is weak, introns are not neutral, in their effect on survival, says CSHLs Michael Zhang, who headed the research team.. To look for selection, co-researcher Chaolin Zhang looked in the ...
Gene can be much larger than unit that codes for protein(as u can conclude)Introns vary while exones are quite conserved(cause selection removes carriers of severe mutations in exones). Very long genes are the result of very long introns! In some techiniques you compare lengths of of alleles. That could be a sign of genetical relation. Could, but not definitely cause same lengh doesnt mean same nucleotide order. But if u compare more polymorphic regions and get covering in size between 2 individuals, the possibility that they are related is higher(again same size doesnt mean same nucleotide order ...
Introns interrupt almost every eukaryotic protein-coding gene, yet how the splicing apparatus interprets the genome during messenger RNA (mRNA) synthesis is poorly understood. We designed microarrays to distinguish spliced from unspliced RNA for each intron-containing yeast gene and measured genomewide effects on splicing caused by loss of 18 different mRNA processing factors. After accommodating changes in transcription and decay by using gene-specific indexes, functional relationships between mRNA processing factors can be identified through their common effects on spliced and unspliced RNA. Groups of genes with different dependencies on mRNA processing factors are also apparent. Quantitative polymerase chain reactions confirm the array-based finding that Prp17p and Prp18p are not dispensable for removal of introns with short branchpoint-to-3′ splice site distances. ...
Supplementary Materials [Supplemental material] jbacter_187_15_5437__index. II introns are genetic retroelements capable of self-splicing and mobility that are common in prokaryotes. Originally discovered in organelles of Read More ...
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A genomic DNA encoding an E8-like gene (CmE8, accession number AB071820) was isolated from melon and its nucleotide sequence was determined. The CmE8 consisted of three exons and two introns. The number and size of the exons and the location of introns were identical to those in tomato E8 gene. The deduced amino acid sequence of CmE8 consisted of 367 amino acids, and it was similar to those of 2-o ...
A catalogue of known hemiascomycetous yeast splicing signals was then used as bait to screen the batch of selected coding sequences, and to validate or not the presence of an intron ...
Intron je nukleotidna sekvenca unutar gena koja se uklanja putem RNK splajsovanja tokom formiranja finalnog RNK proizvoda.[1][2] Termin intron se odnosi na DNK sekvencu unutar gena, i odgovarajuću sekvencu RNK transkripta.[3] Sekvence koje se spajaju u finalnu maturiranu RNK nakon RNK splajsovanja su eksoni. Introni su prisutni u genima većine organizama i mnogim virusima. Oni se mogu naći u širokom nizu gena, uključujući one koji kodiraju proteine, ribozomsku RNK (rRNK), i transportnu RNK (tRNK). Tokom formirana proteina iz gena koji sadrže introne, dolazi do RNK splajsovanja nakon transkripcije i pre translacije. Reč intron je izvedena iz termina intrageni region, i.e. region unutar gena. ...
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英創科技股份有限公司(Intron Scientific Co., Ltd.)成立於1995年7月,『INTRON』原意是人類遺傳的主要組成DNA中一個重要成分代表『英創科技』的核心精神在於建立以「人」為公司最重要資產的核心價值觀,包括員工、顧客供應商以及投資人。實收資本額三千五百萬元整。 將最新
Mobile group II introns are ribozymes and retroelements that probably originate from bacteria. Sinorhizobium meliloti, the nitrogen-fixing endosymbiont of legumes of genus Medicago, harbors a large number of these retroelements. One of these elements, RmInt1, has been particularly successful at colonizing this multipartite genome. Many studies have improved our understanding of RmInt1 and phylogenetically related group II introns, their mobility mechanisms, spread and dynamics within S. meliloti and closely related species. Although RmInt1 conserves the ancient retroelement behavior, its evolutionary history suggests that this group II intron has played a role in the short- and long-term evolution of the S. meliloti genome. We will discuss its proposed role in genome evolution by controlling the spread and coexistence of potentially harmful mobile genetic elements, by ectopic transposition to different genetic loci as a source of early genomic variation and by generating sequence variation after a very
TY - JOUR. T1 - A functional role for some Fugu introns larger than the typical short ones. T2 - The example of the gene coding for ribosomal protein S7 and snoRNA U17. AU - Cecconi, Francesco. AU - Crosio, Claudia. AU - Mariottini, Paolo. AU - Cesareni, Gianni. AU - Giorgi, Marcello. AU - Brenner, Sydney. AU - Amaldi, Francesco. PY - 1996. Y1 - 1996. N2 - The compact genome of Fugu rubripes, with its very small introns, appears to be particularly suitable to study intron-encoded functions. We have analyzed the Fugu gene for ribosomal protein S7 (formerly S8, see Note), whose Xenopus homolog contains in its introns the coding sequences for the small nucleolar RNA U17. Except for intron length, the organization of the Fugu S7 gene is very similar to that of the Xenopus counterpart. The total length of the Fugu S7 gene is 3930 bp, compared with 12691 bp for Xenopus. This length difference is uniquely due to smaller introns. Although short, the six introns are longer than the ~100 bp size of most ...
Members of this protein family are multifunctional proteins encoded in most examples of bacterial group II introns. These group II introns are mobile selfish genetic elements, often with multiple highly identical copies per genome. Member proteins have an N-terminal reverse transcriptase (RNA-directed DNA polymerase) domain (PF00078) followed by an RNA-binding maturase domain (PF08388). Some members of this family may have an additional C-terminal DNA endonuclease domain that this model does not cover. A region of the group II intron ribozyme structure should be detectable nearby on the genome by Rfam model RF00029 ...
Although large scale informatics studies on introns can be useful in making broad inferences concerning patterns of intron gain and loss, more specific questions about intron evolution at a finer scale can be addressed using a gene family where structure and function are well known. Genome wide surveys of tetraspanins from a broad array of organisms with fully sequenced genomes are an excellent means to understand specifics of intron evolution. Our approach incorporated several new fully sequenced genomes that cover the major lineages of the animal kingdom as well as plants, protists and fungi. The analysis of exon/intron gene structure in such an evolutionary broad set of genomes allowed us to identify ancestral intron structure in tetraspanins throughout the eukaryotic tree of life. We performed a phylogenomic analysis of the intron/exon structure of the tetraspanin protein family. In addition, to the already characterized tetraspanin introns numbered 1 through 6 found in animals, three ...
Two types of spliceosomes catalyze splicing of pre-mRNAs. The major U2-type spliceosome is found in all eukaryotes and removes U2-type introns, which represent more than 99% of pre-mRNA introns. The minor U12-type spliceosome is found in some eukaryotes and removes U12-type introns, which are rare and have distinct splice consensus signals. The U12-type spliceosome consists of several small nuclear RNAs and associated proteins. This gene encodes a 65K protein that is a component of the U12-type spliceosome. This protein contains two RNA recognition motifs (RRMs), suggesting that it may contact one of the small nuclear RNAs of the minor spliceosome. [provided by RefSeq, Jul 2008 ...
The fission yeast genome, which contains numerous short introns, is an apt model for studies on fungal splicing mechanisms and splicing by intron definition. Here we perform a domain analysis of the evolutionarily conserved Schizosaccharomyces pombe pre-mRNA-processing factor, SpPrp18. Our mutational and biophysical analyses of the C-terminal alpha-helical bundle reveal critical roles for the conserved region as well as helix five. We generate a novel conditional missense mutant, spprp18-5. To assess the role of SpPrp18, we performed global splicing analyses on cells depleted of prp18(+) and the conditional spprp18-5 mutant, which show widespread but intron-specific defects. In the absence of functional SpPrp18, primer extension analyses on a tfIId(+) intron 1-containing minitranscript show accumulated pre-mRNA, whereas the lariat intron-exon 2 splicing intermediate was undetectable. These phenotypes also occurred in cells lacking both SpPrp18 and SpDbr1 (lariat debranching enzyme), a genetic ...
BackgroundThe genome of the pico-eukaryotic (bacterial-sized) prasinophyte green alga Ostreococcus lucimarinus has one of the highest gene densities known in eukaryotes, yet it contains many introns. Phylogenetic studies suggest this unusually compact genome (13.2 Mb) is an evolutionarily derived state among prasinophytes. The presence of introns in the highly reduced O. lucimarinus genome appears to be in opposition to simple explanations of genome evolution based on unidirectional tendencies, either neutral or selective. Therefore, patterns of intron retention in this species can potentially provide insights into the forces governing intron evolution.Methodology/Principal FindingsHere we studied intron features and levels of expression in O. lucimarinus using expressed sequence tags (ESTs) to annotate the current genome assembly. ESTs were assembled into unigene clusters that were mapped back to the O. lucimarinus Build 2.0 assembly using BLAST and the level of gene expression was inferred from the
TY - JOUR. T1 - An alternative route for the folding of large RNAs. T2 - Apparent two-state folding by a group II intron ribozyme. AU - Su, Linhui Julie. AU - Brenowitz, Michael. AU - Pyle, Anna Marie. N1 - Funding Information: The authors thank Tobin Sosnick, Art Palmer, Eric Gouaux, and Andrew Miranker for insightful advice and suggestions, Peter Moore for suggesting hydrodynamic techniques for studying group II introns, Alex de Lencastre and Christina Waldsich for helpful discussions on the manuscript, and Rich Olson for advice on analytical ultracentrifugation. Funding for the Jasco J810 Spectropolarimeter was obtained from NIH grant GM34509 to Koji Nakanishi. Funding for the Beckman XL-I centrifuges were obtained from NIH shared instrumentation grant S10 RR12848 to Columbia University and GM54160 to Donald Engelman (Yale University). We acknowledge funding from NIH to L.J.S. (Biophysics Training Grant T32 GM08281), M.B. (GM52348), and A.M.P. (RO1 GM50313). A.M.P. is an Investigator of the ...
DNA is made up of different units called nucleotides. There are a variety of four different nucleotides that make up the polymer that is DNA[1]. DNA consists of two different regions, one being exons and the other introns. The regions of exons in the DNA consist of fewer nucleotides than the regions of introns and are the regions that code for proteins[2]. It is also now thought that enhancer sequences for regulation of gene transcription is not just found in introns but also exons.[3]. Exons are the coding regions of a gene and are separated by regions of introns; they are copied during transcription (along with introns) to produce pre-mRNA[4] ...
TY - JOUR. T1 - Tissue-specific splicing regulator Fox-1 induces exon skipping by interfering E complex formation on the downstream intron of human F1γ gene. AU - Fukumura, Kazuhiro. AU - Kato, Ayako. AU - Jin, Yui. AU - Ideue, Takashi. AU - Hirose, Tetsuro. AU - Kataoka, Naoyuki. AU - Fujiwara, Toshinobu. AU - Sakamoto, Hiroshi. AU - Inoue, Kunio. PY - 2007/8/1. Y1 - 2007/8/1. N2 - Fox-1 is a regulator of tissue-specific splicing, via binding to the element (U)GCAUG in mRNA precursors, in muscles and neuronal cells. Fox-1 can regulate splicing positively or negatively, most likely depending on where it binds relative to the regulated exon. In cases where the (U)GCAUG element lies in an intron upstream of the alternative exon, Fox-1 protein functions as a splicing repressor to induce exon skipping. Here we report the mechanism of exon skipping regulated by Fox-1, using the hF1γ gene as a model system. We found that Fox-1 induces exon 9 skipping by repressing splicing of the downstream intron 9 ...
Author: Britanova, O. et al.; Genre: Journal Article; Published in Print: 2002-07; Keywords: cortex; transcription factor; subtraction; Sey; reeler; mutant|br/|; Title: The mouse Laf4 gene: Exon/intron organization, cDNA sequence, alternative splicing, and expression during central nervous system development
The classification of human gene sequences into exons and introns is a difficult problem in DNA sequence analysis. In this paper, we define a set of features, called the simple Z (SZ) features, which is derived from the Z-curve features for the recognition of human exons and introns. The classification results show that SZ features, while fewer in numbers ~three in total!, can preserve the high recognition rate of the original nine Z-curve features. Since the size of SZ features is one-third of the Z-curve features, the dimensionality of the feature space is much smaller, and better recognition efficiency is achieved. If the stop codon feature is used together with the three SZ features, a recognition rate of up to 92% for short sequences of length ,140 bp can be obtained ...
In contrast to bacteria which have no introns, eukaryotes (cells with a nucleus) have introns which are intervening sequences within genes which get spliced out when genes are transcribed and are not expressed in the protein. In contrast, exons are the sequences within a gene which do get expressed and translated into protein. Intergenic DNA, as the name suggests, is DNA between genes which does not code for proteins. Hope this helps gabriel vargas md/phd References Genes VII by Benjamin Lewin ...
This is a pretty good article on the origin of the spliceosome from self-splicing introns: Vosseberg J, Snel B. Domestication of self-splicing introns during eukaryogenesis: the rise of the complex spliceosomal machinery. Biol Direct. 2017 Dec 1;12(1):30. DOI:10.1186/s13062-017-0201-6 There are many interesting references given in that article also, for example on spliceosomal diversity. There are simple protozoan parasites known with as few as 27 introns in their entire genomes, and highly s...
Comparative analysis of exon/intron organization of genes and their resulting protein structures is important for understanding evolutionary relationships between species, rules of protein organization, and protein functionality. We present SEDB, the Structural Exon Database, with a web interface, an application which allows users to retrieve the exon/intron organization of genes and map the location of the exon boundaries and intron phase onto a multiple structural alignment. SEDB is linked with Friend, an integrated analytical multiple sequence/structure viewer, which allows simultaneous visualization of exon boundaries on structure and sequence alignments. With SEDB researchers can study the correlations of gene structure with the properties of the encoded three-dimensional protein structures across eukaryotic organisms ...
import pysam from collections import Counter from CGAT import GTF, IOTools def calculateSplicingIndex(bamfile, gtffile, outfile): bamfile = pysam.AlignmentFile(bamfile) counts = Counter() for transcript in GTF.transcript_iterator( GTF.iterator(IOTools.openFile(gtffile))): introns = GTF.toIntronIntervals(transcript) for intron in introns: reads = bamfile.fetch( reference=transcript[0].contig, start=intron[0], end=intron[1]) for read in reads: if N in read.cigarstring: blocks = read.get_blocks() starts, ends = zip(*blocks) if intron[0] in ends and intron[1] in starts: counts[Exon_Exon] += 1 else: counts[spliced_uncounted] += 1 elif (read.reference_start ,= intron[0] - 3 and read.reference_end ,= intron[0] + 3): if transcript[0].strand == +: counts[Exon_Intron] += 1 else: counts[Intron_Exon] += 1 elif (read.reference_start ,= intron[1] - 3 and read.reference_end ,= intron[1] + 3): if transcript[0].strand == +: counts[Intron_Exon] += 1 else: counts[Exon_Intron] += 1 else: ...
By Michael Marshall. Patches of seemingly meaningless DNA dotted throughout the genome might actually have a function: helping cells to survive starvation.. Two studies published in Nature on 16 January suggest that these stretches of non-coding DNA called introns help to control the rate at which cells grow, conserving energy when food becomes scarce.. Genes carry the information needed to make proteins. But many genes contain introns: sequences of non-coding DNA, the vast majority of which dont appear to do anything.. Some researchers suspected introns did more than meets the eye.. In one of the latest studies1, Sherif Abou Elela, a microbiologist at the University of Sherbrooke in Quebec, Canada, and his colleagues examined bakers yeast (Saccharomyces cerevisiae), whose DNA has 295 introns. They spent ten years meticulously creating hundreds of yeast strains, each missing just one of its introns.. Continue reading by clicking the name of the source below.. ...
Responsibilities: He conducted PCR and DNA sequencing experiments to gather DNA sequence data from the b-fibrinogen gene for selected avian orders. DNA sequence was used in subsequent phylogenetic analyses. Developed three additional novel intron sequences from other nuclear genes for use in further phylogenetic analyses of avian species. Evaluated the statistical comparison of the base composition, distribution of substitutions, transition / transversion ratio, degree of homoplasy, and variation in substitution rates among the introns. He additionally explored DNA sequence patterns in introns of nuclear genes for the purpose of locating possible gene promoter and transcription factor binding sites and their possible link to gene expression ...
p,,strong,Frameshift introns,/strong, are the length of 1, 2, 4, or 5 basepairs. They are introduced by the Ensembl ,a href=../../../info/genome/genebuild/index.html,genebuild,/a, in order to fit the cDNA sequence to the genome.,/p,Frameshift introns occur at intron number(s) 16. ...
For many types of analyses, data about gene structure and locations of non-coding regions of genes are required. Although a vast amount of genomic sequence data is available, precise annotation of genes is lacking behind. Finding the corresponding gene of a given protein sequence by means of conventional tools is error prone, and cannot be completed without manual inspection, which is time consuming and requires considerable experience. Scipio is a tool based on the alignment program BLAT to determine the precise gene structure given a protein sequence and a genome sequence. It identifies intron-exon borders and splice sites and is able to cope with sequencing errors and genes spanning several contigs in genomes that have not yet been assembled to supercontigs or chromosomes. Instead of producing a set of hits with varying confidence, Scipio gives the user a coherent summary of locations on the genome that code for the query protein. The output contains information about discrepancies that may result
1. In the context of a new mammalian model organism recently sequenced and annotated, gene YFG has 3 introns and 4 exons. Databases show that there are 3 different lengths of cDNA sequences associated with Gene YFG. One of these cDNA sequences has three out of four exons plus additional nucleotide sequence at the 3 end of the cDNA. This part codes for an extra 123 amino acids. Annotated gene UB2, appears immediately downstream of YFG. UB2 has a single exon coding for 123 amino acids matching the cDNA. There is no cDNA in your database encoding for a UB2 gene with these 123 amino acids at the N-terminus ...
To assess whether the discrepancy between the protein and mRNA levels was due to the presence of variant embryonic proinsulin transcripts, we carried out a detailed RT-PCR study during gastrulation, neurulation and early organogenesis (Fig 2). PCR with the P3 and P5 primers showed two amplification products (Fig 2A,B). Cloning and sequencing of these PCR products showed that the larger band corresponded to an alternatively spliced isoform (Pro1B1) of the embryonic proinsulin transcript; it retained intron 1 (717 nt) in the 5′ UTR, but spliced out intron 2 (3,432 nt). Both spliced and intron‐retained embryonic transcripts were polyadenylated, since oligo‐dT was used in the RT reaction. The intron 1 splicing pattern is developmentally regulated; the intron 1‐containing isoform was nearly undetectable during gastrulation (st. 4), and the percentage of intron 1 retention increased throughout neurulation (st. 8-10) and organogenesis (st. 12; Fig 2B,C). No PCR products were detected in the ...
Mitochondrial Mg (super.2+) homeostasis is critical for group II intron splicing in vivo. Molecular genetic analysis of the heterodimeric splicing factor U2AF: the RS domain on either the large or small Drosophila subunit is dispensable in vivo
Chloroplast RNA splicing 2 (CRS2) is a nuclear-encoded protein required for the splicing of nine group II introns in maize chloroplasts. CRS2 functions in the context of splicing complexes that include one of two CRS2-associated factors (CAF1 and CAF2). The CRS2-CAF1 and CRS2-CAF2 complexes are requ …
The mdm2 gene is a target for transcriptional activation by the p53 tumor suppressor gene product. Previous work has revealed that the mouse mdm2 gene contains two promoters: one is located upstream to the gene and is active in the absence of p53, the other resides within the first intron and requires p53 for transcriptional activity. To determine whether this unique promoter activation pattern is biologically important, we investigated the structure and function of the corresponding region of the human mdm2 (hmdm2) gene. We report here that the hmdm2 gene also contains an intronic, p53-dependent promoter. The structural features of this promoter are highly conserved between mouse and man, as opposed to the lack of conservation of the first exon. This promoter is triggered in vivo in the presence of activated wild type p53, leading to the production of novel mRNA species. The intronic hmdm2 promoter contains two tandem p53 binding elements. Deletion analysis suggests that optimal promoter
Reverse transcriptases (RTs) are usually thought of as eukaryotic enzymes, but they are also present in bacteria and likely originated in bacteria and migrated to eukaryotes. Only three types of bacterial retroelements have been substantially characterized: group II introns, diversity-generating retroelements, and retrons. Recent work, however, has identified a myriad of uncharacterized RTs and RT-related sequences in bacterial genomes, which exhibit great sequence diversity and a range of domain structures. Apart from group II introns, none of these putative RTs show evidence of active retromobility. Instead, available information suggests that they are involved in useful processes, sometimes related to phages or phage resistance. This article reviews our knowledge of both characterized and uncharacterized RTs in bacteria. The range of their sequences and genomic contexts promises the discovery of new biochemical reactions and biological phenomena.
RNA Splicing Definition RNA splicing is a form of RNA processing in which a newly made precursor messenger RNA (mRNA) is transformed into a mature RNA by removing the non-coding sequences termed introns. The process of RNA splicing involves the … Read more. ...
Exon sequences are conserved, but intron sequences vary, Organization of Genetic Material Split Genes, Overlapping Genes and Pseudogenes, Genetics
This sequence change falls in intron 3 of the SPRED1 gene. It does not directly change the encoded amino acid sequence of the SPRED1 protein. This variant is not present in population databases (ExAC no frequency) and has not been reported in the literature in individuals with a SPRED1-related disease. Algorithms developed to predict the effect of sequence changes on RNA splicing suggest that this variant may alter RNA splicing, but this prediction has not been confirmed by published transcriptional studies. In summary, this is a novel intronic change with uncertain impact on splicing. It has been classified as a Variant of Uncertain Significance ...
I am looking at RNA-seq data, which I have little experience in. I notice that for many genes, there are reliable alignments (i.e. with high mapping quality) to introns. I understand that some of them are due to unannotated transcripts, but in many regions, this does not seem to be the major cause. The intronic read hits do not seem to be purely caused by alignments artifacts, either, because the pattern is tissue specific (though this is not a compelling evidence). Another possible explanation is that this observation is due to noisy transcripts (Pickrell et al, 2010), but this seems to be a big effect: for some long genes, there are far more intronic hits than exonic hits.. I guess those who study RNA-seq data must have noticed the intronic hits for years. What is cause of the large amount of intronic read hits? Is it caused by alignment/library prep artifacts or noisy transcription? Are there papers addressing this? Thanks.. EDIT: my conclusion. I was looking at ERR030882 from Illumina ...
A transcript is the operational unit of a gene. In a genomic context, transcripts consist of one or more exons, with adjoining exons being separated by introns. The exons/introns are transcribed and then the introns spliced out. Transcripts may or may not encode a proteinGene transcripts ...
Once transcription is complete, there are further controls that allow the network of enzymes and genes to control itself. Im not going to list all of them, but one that cannot be left out involves alternative splicing of RNA. This is a process in which the transcribed RNA is edited, usually removing a number of sections called introns, while creating the final mRNA. Which introns are removed, and sometimes where their boundaries are set, determines the sequence of the final mRNA, and thus the character of the protein. Alternative splicing can be affected by enzymes, but also by non-coding RNAs of various types and provenance, including those snipped out of the introns of other genes. A description of some of the ways in which alternative splicing can be regulated may be found in Regulation of Alternative Splicing: More than Just the ABC by Amy E. House and Kristen W. Lynch. It may turn out that the number of data connections that affect protein (enzyme) concentration via regulation of internal ...
This sequence change falls in intron 14 of the PNKP gene. It does not directly change the encoded amino acid sequence of the PNKP protein, but it affects a nucleotide within the consensus splice site of the intron. This variant is present in population databases (rs776617733, ExAC 0.04%). This variant has not been reported in the literature in individuals with PNKP-related conditions. Nucleotide substitutions within the consensus splice site are a relatively common cause of aberrant splicing (PMID: 17576681, 9536098). Algorithms developed to predict the effect of sequence changes on RNA splicing suggest that this variant is not likely to affect RNA splicing, but this prediction has not been confirmed by published transcriptional studies. In summary, the available evidence is currently insufficient to determine the role of this variant in disease. Therefore, it has been classified as a Variant of Uncertain Significance ...
Parameters: -f ,filename, potential splice sites in gff format -g ,filename, genome file in fasta format -c ,integer, defines the number of potential splice site every potential splice site itself is compared with -t ,float, has to be between 0 and 1 and defines how much the average coverage may differ -m ,integer, defines how many bases around the splice site should be checked -d enables debugging output -i ,integer, maximum length an Intron can be, default 500000 (human genome ...
Read Variants in an Hdac9 intronic enhancer plasmid impact Twist1 expression in vitro, Mammalian Genome on DeepDyve, the largest online rental service for scholarly research with thousands of academic publications available at your fingertips.
Loren I. Petrich writes: , , This does not look like the result of spotaneous generation, ,unless one allows for extreme improbabilities, so it is presumed that ,there has been a lot of evolution behind it, evolution that may have ,left some vestiges, in the fashion of the numerous vestigial features ,generated by later evolution (I wonder if anyone has compiled a ,reasonably comprehensive list). Interesting request. How many molecular fossils can you name? Heres a start: rRNA performs catalytic functions in ribosomes (several papers in Science in the last few weeks) tRNA CCA adding enzyme is the first telomerase (Nancy Maizels and Alan Weiner in PNAS a few years ago) self-splicing introns and the role of snRNAs in other intron splicing NTPs as energy-storage media other nucleoside-based cofactors (NAD, CoA, etc.) mRNA , , A system where there are two kinds of nucleic acids and where ,RNA was the original molecule, with DNA a specialization for long-term ,information storage. This is from ...
originalDATA1ofFigS3C.tif : Full-length western blotting images used in Fig S3C (HEK293 cells). originalDATA2ofFigS3C.tif : Full-length western blotting images used in Fig S3C (U2OS cells). originalDATA3ofFigS7B.tif : Full-length western blotting images used in Fig S7B.
Genes in eukaryotic organisms are frequently interrupted by non-coding segments called introns. Before the protein can be produced, the entire length of each gene including the introns, is transcribed to produce precursor messenger RNA (pre-mRNA).
Im working on a chapter about pervasive transcription and how it relates to the junk DNA debate. I found a short review in Nature from 2002 so I decided to see how much progress weve made in the past 15 years.. Most of our genome is transcribed at some time or another in some tissue. Thats a fact weve known about since the late 1960s (King and Jukes, 1969). We didnt know it back then, but it turns out that a lot of that transcription is introns. In fact, the observation of abundant transcription led to the discovery of introns. We have about 20,000 protein-coding genes and the average gene is 37.2 kb in length. Thus, the total amount of the genome devoted to these genes is about 23%. Thats the amount thats transcribed to produce primary transcripts and mRNA. There are about 5000 noncoding genes that contribute another 2% so genes occupy about 25% of our genome ...
Im working on a chapter about pervasive transcription and how it relates to the junk DNA debate. I found a short review in Nature from 2002 so I decided to see how much progress weve made in the past 15 years.. Most of our genome is transcribed at some time or another in some tissue. Thats a fact weve known about since the late 1960s (King and Jukes, 1969). We didnt know it back then, but it turns out that a lot of that transcription is introns. In fact, the observation of abundant transcription led to the discovery of introns. We have about 20,000 protein-coding genes and the average gene is 37.2 kb in length. Thus, the total amount of the genome devoted to these genes is about 23%. Thats the amount thats transcribed to produce primary transcripts and mRNA. There are about 5000 noncoding genes that contribute another 2% so genes occupy about 25% of our genome ...
Alternative splicing was the first phenomenon scientists discovered that made them realize that genomic complexity cannot be judged by the number of protein-coding genes. During alternative splicing, which occurs after transcription and before translation, introns are removed and exons are spliced together to make an mRNA molecule. However, the exons are not necessarily all spliced back together in the same way. Thus, a single gene, or transcription unit, can code for multiple proteins or other gene products, depending on how the exons are spliced back together. In fact, scientists have estimated that there may be as many as 500,000 or more different human proteins, all coded by a mere 20,000 protein-coding genes. ...
Turunen, J. J.; Will, C. L.; Grote, M.; Luehrmann, R.; Frilander, M. J.: The U11-48K protein contacts the 5 splice site of U12-Type introns and the U11-59K protein. Molecular and Cellular Biology 28 (10), pp. 3548 - 3560 (2008 ...
There are many classic examples of evidence that support evolution, such as endogenous retroviruses or transitional fossils, but I would like to focus on another piece of evidence that I think is just as powerful and hop…
Ive been sewing since I was 4. Barbie doll clothes made way for maxi skirts, to mini skirts, to 3 piece suits. Upholstered pieces followed, and then I learned how to quilt ...
The classical gene codes for a protein; the genetic code is transcribed into a strand of RNA by RNA polymerase. This RNA, known as pre-messenger RNA, undergoes splicing where the introns are removed. Once completed, the messenger RNA is transported to the ribosomes in the cytoplasm for translation into protein ...
There are five tracks in this figure. The x-axis at the bottom shows the sequence coordinates on this chromosome in the human genome. The top track shows the organization of genes that cover this region. In this case we can see from the arrowhead at the left end that BRCA1 is encoded on the reverse strand of the DNA, running right to left.. The small blue blocks represent the exons in this gene, separated by the much larger introns. The track below this shows the location of sequence repeats, with the colors representing different types. The genome is packed full of these so-called junk sequences, the functions of which are still unclear. Notice that the repeats account for most, but not all, of the intron sequences. The two large tracks with the peaks and valleys display how well the human sequence is conserved in the genomes of mouse and rat, respectively. The similarity plot is truncated at 50% so any peaks shown indicate strong similarity. These two plots look broadly the same, indicating ...
The G of the donor site is joined covalently to the A of the branch site. This structure is excised at the 3 end of the acceptor site, and the ends of the two adjacent exon equivalents are joined. ...
View Notes - Lecture.14.Fall.2013 from BIOLOGY 115 at San Jose State. in eukaryotes are colinear within exons, but are interrupted by noncoding sequences Introns vary in length, and are longer, on
Introns is a remix album by the American rock band LCD Soundsystem, released in March 2006 through DFA as a digital download. ...
... tRNA introns, group I introns, group II introns, and spliceosomal introns (see below). Introns are rare in Bacteria and Archaea ... and possibly to spliceosomal introns. Nuclear pre-mRNA introns (spliceosomal introns) are characterized by specific intron ... Intron transfer has been hypothesized to result in intron gain when a paralog or pseudogene gains an intron and then transfers ... This intron-containing mRNA is then reverse transcribed and the resulting intron-containing cDNA may then cause intron gain via ...
The Database for Bacterial Group II Introns is a repository of full-length, non-redundant group II introns present in bacterial ... group II intron Candales, Manuel A; Duong Adrian; Hood Keyar S; Li Tony; Neufeld Ryan A E; Sun Runda; McNeil Bonnie A; Wu Li; ... The database is first established in 2002 with roughly 40 introns. In less than 10 years, the database has expanded to 400 ... In addition, it contains a list of intron insertion sites, DNA sequences, protein-encoding sequences, as well as RNA secondary ...
The bZIP intron candida is an unconventional bZIP intron located in the HAC1 mRNA in a subgroup of fungi from Saccharomycetales ... Splicing performed by Ire1 results in excision of a very long intron that was first described in Candida parapsilosis. Hooks KB ... bZIP intron ascomycota-like). The consensus structure consists of two well conserved hairpins with loop regions defining the ... Griffiths-Jones S (2011). "Conserved RNA structures in the non-canonical Hac1/Xbp1 intron". RNA Biol. 8 (4): 552-556. doi: ...
... s identify introns along pre-tRNAs and carry out the proper excision mechanism to remove those introns ... tRNA-intron lyase (EC 4.6.1.16, tRNA intron endonuclease, transfer ribonucleate intron endoribonuclease, tRNA splicing ... and an intron with a 2',3'-cyclic phosphate and a 5'-hydroxyl terminus. The use of tRNA-intron endonuclease in pre-tRNA intron ... Splicing on both the 3' and 5' ends of the intron. tRNA-intron lyase requires a level of specificity to the splice site on the ...
The small T intron is an intron, that is used in some plasmid vectors, in order to induce gene expression in mammalian cells. ... The function of this intron in the vectors is unknown, but it is theorized that it might be involved in splicing or translation ... Hunt AG, Mogen BD, Chu NM, Chua NH (1991). "The SV40 small t intron is accurately and efficiently spliced in tobacco cells". ... Huang MT, Gorman CM (1990). "The simian virus 40 small-t intron, present in many common expression vectors, leads to aberrant ...
One feature of Intron Depot 1 is that all of the works are presented with a small aside from Shirow as to his thoughts on them ... Intron Depot 1 in two spots in particular is quite graphic. One panel involves a graphic drawing of a lesbian ménage à trois, ... Intron Depot 1 (イントロンデポ) is a collection of Masamune Shirow's full color works. The volume itself is 148 210 mm x 285 mm pages ... Everything from Appleseed to Orion are well represented in Intron Depot 1, some pictures are reproductions of paintings, others ...
The bZIP intron saccharomycetales is an unconventional bZIP intron located in the HAC1 mRNA in most budding yeast belonging to ... Hooks KB, Griffiths-Jones S (2011). "Conserved RNA structures in the non-canonical Hac1/Xbp1 intron". RNA Biol. 8 (4): 552-556 ...
The bZIP intron animal is an unconventional bZIP intron in animals located in the mRNA of Xbp1 orthologs. The RNA structure ... Intron is usually 23 or 26 nt long and it is excised by endoribonuclease Ire1 encoded by ERN1 gene in response to ER stress. ... Hooks KB, Griffiths-Jones S (2011). "Conserved RNA structures in the non-canonical Hac1/Xbp1 intron". RNA Biol. 8 (4): 552-556 ...
The bZIP intron plant is an unconventional bZIP intron in plants located in the mRNA of bZIP60 orthologs. The consensus RNA ... Majority of the plants contain also a nested spliceosomal intron located at the base of 3' hairpin. The unconventional splicing ... Hooks KB, Griffiths-Jones S (2011). "Conserved RNA structures in the non-canonical Hac1/Xbp1 intron". RNA Biol. 8 (4): 552-556 ... structure is very similar to the animal variant with short, usually 23 nt intron defined by the loop regions of the conserved ...
If the intron can no longer enhance expression, then inclusion of the intron in the transcript is important, and the intron ... is the ability of an intron sequence to enhance the expression of a gene containing that intron. In particular, the intron must ... The position of an intron within the transcript is also important - the closer an intron is to the start (5' end) of a ... Rose, Alan B. (2004-12-01). "The effect of intron location on intron-mediated enhancement of gene expression in Arabidopsis". ...
... (U12DB) is a biological database of containing the sequence of eukaryotic introns that are spliced out by a ... These U12-dependent introns are under-represented in genome annotations because they often have non canonical splice sites. ... Release 1 of the database contains 6,397 known and predicted U12-dependent introns across 20 species. Alioto, Tyler S (Jan 2007 ... "U12DB: a database of orthologous U12-type spliceosomal introns". Nucleic Acids Res. England. 35 (Database issue): D110-5. doi: ...
The bZIP intron ascomycota is an unconventional bZIP intron found in some of the Ascomycota fungi, mainly in filamentous fungi ... The unconventional splicing in this group results in excising introns of typical length 20 or 23 nt and it was first described ... Hooks KB, Griffiths-Jones S (2011). "Conserved RNA structures in the non-canonical Hac1/Xbp1 intron". RNA Biol. 8 (4): 552-556 ...
The bZIP intron basidiomycota is an unconventional bZIP intron found mainly in the Basidiomycota and some Mucoromycotina fungi ... In Basidiomycota, splicing results in excised introns from 20 to 101 nt in length and it was first described in Cryptococcus ... Hooks KB, Griffiths-Jones S (2011). "Conserved RNA structures in the non-canonical Hac1/Xbp1 intron". RNA Biol. 8 (4): 552-556 ...
... is a class of introns found in mRNA genes of chloroplasts in euglenid protists. They have a conventional group ... Group III introns are much shorter than other self-splicing intron classes, ranging from 95 to 110 nucleotides amongst those ... In 1994, discovery of a group III intron with a length of one order of magnitude longer indicated that length alone is not the ... In 1989, David A. Christopher and Richard B. Hallick found a few more examples and proposed the name "Group III introns" to ...
The Exon-Intron Database (EID) is a database of spliced mRNA sequences. Alternative splicing Exon Intron Saxonov, S; Daizadeh I ... Fedorov A; Gilbert W (Jan 2000). "EID: the Exon-Intron Database-an exhaustive database of protein-coding intron-containing ...
Database for bacterial group II introns Intron Splice site Nuclear introns Group I intron Group III intron Twintron LtrA ... Protein machinery is required for splicing in vivo, and long-range intron-intron and intron-exon interactions are important for ... The first intron to be identified as distinct from group I was the ai5γ group IIB intron, which was isolated in 1986 from a pre ... In contrast to group I introns, intron excision occurs in the absence of GTP and involves the formation of a lariat, with an A- ...
The consensus intron is very short in Metazoa (20, 23 or 26 nt). However, yeast species have a long (>100 nt) intron in HAC1. ... The bZIP intron RNA motif is an RNA structure guiding splicing of a non-canonical intron from bZIP-containing genes called HAC1 ... Recognition of the intron splice sites is mediated by a base-paired secondary structure of the mRNA that forms at the exon/ ... intron boundaries. Splicing of the bZIP intron is a key regulatory step in the unfolded protein response (UPR). The Ire- ...
Intron Group I Intron Sequence and Structure Database Splice site Nuclear introns Group II intron Group III intron Twintron ... Both intron-early and intron-late theories have found evidences in explaining the origin of group I introns. Some group I ... Group I introns often have long open reading frames inserted in loop regions. Splicing of group I introns is processed by two ... A small number of group I introns are also found to encode a class of proteins called maturases that facilitate the intron ...
Intron-encoded endonuclease I-Sce I is a homing endonuclease. The enzyme is used in biotechnology as a meganuclease. It ... I-SceI is coded by introns. It is present in the mitochondria of yeast Saccharomyces cerevisiae. New England Biolabs site ...
Jacquier A, Dujon B (June 1985). "An intron-encoded protein is active in a gene conversion process that spreads an intron into ... "Intron 5 alpha of the COXI gene of yeast mitochondrial DNA is a mobile group I intron". Nucleic Acids Res. 20 (15): 4069-76. ... "Structural conservation among three homologous introns of bacteriophage T4 and the group I introns of eukaryotes". PNAS. 85 (4 ... Eddy SR, Gold L (June 1991). "The phage T4 nrdB intron: a deletion mutant of a version found in the wild". Genes Dev. 5 (6): ...
Notches indicate introns. Chloroplast DNA (cpDNA) is the DNA located in chloroplasts, which are photosynthetic organelles ...
Introns and inteins. Intragenomic conflict: Homing endonuclease genes. I-CreI homing endonuclease. Databases and lists of ...
Notches indicate introns. Gene maps help describe the spatial arrangement of genes on a chromosome. Genes are designated to a ...
Notches indicate introns. With few exceptions, most chloroplasts have their entire chloroplast genome combined into a single ... Unlike prokaryotic DNA molecules, chloroplast DNA molecules contain introns (plant mitochondrial DNAs do too, but not human ...
... contains 18 introns. There are 2 non overlapping alternative last exons. The transcripts appear to differ by truncation of ... MCM6 produces, by alternative splicing, 3 different transcripts, all with introns, putatively encoding 3 different protein ... located in two of the MCM6 introns, approximately 14 kb (-13910) and 22 kb (-22018) upstream of LCT. The (-13910) region, in ...
Bürglin TR, Barnes TM (1992). "Introns in sequence tags". Nature. 357 (6377): 367-8. Bibcode:1992Natur.357..367B. doi:10.1038/ ...
When testing the effect of unc-5::intron::unc-5 transgene on a mislocalization defect in UNC-5 mutant animals at 25 °C a ...
When testing the effect of unc-5::intron::unc-5 transgene on a mislocalization defect in UNC-5 mutant animals at 25 °C a ...
The NFR5 gene lacks introns. First the cell membrane is depolarized and the root hairs start to swell and cell division stops. ...
PEG-Intron): learn about side effects, dosage, special precautions, and more on MedlinePlus ... Peginterferon Alfa-2b (PEG-Intron). pronounced as (peg in ter feer on) ...
Challenging this assumption, a recent study has found a reduction in the mutation rate in exons compared to introns in somatic ... Evidence that somatic mutation rates in introns exceed those in exons challenges the molecular evolution tenet that mutation ... we find no reduction in the mutation rate in exons compared to introns in the germline. Therefore, there is no evidence that ... including the detection of selection when using introns as proxies for neutrality. Here we compile and analyze published ...
The structure of I-Crel, a group I intron-encoded homing endonuclease.. Heath, P.J., Stephens, K.M., Monnat Jr., R.J., Stoddard ... The structure of I-Crel provides the first view of a protein encoded by a gene within an intron. This endonuclease recognizes a ... The structure of I-Crel provides the first view of a protein encoded by a gene within an intron. This endonuclease recognizes a ... The conserved LAGLIDADG motif, which is found in many mobile intron endonucleases, maturases and inteins, forms a novel helical ...
INTRON® A (In-tron-aye). (Interferon alfa-2b, recombinant). If you are taking INTRON A with REBETOL, also read the Medication ... INTRON A may cause serious side effects including: * See "What is the most important information I should know about INTRON A?" ... What is INTRON A? INTRON A is a prescription medicine that is used: *to treat adults with a blood cancer called hairy cell ... Do not use INTRON A for a condition for which it was not prescribed. Do not give INTRON A to other people, even if they have ...
... and Partners - published on openPR.com ... SGS INTRON will attend the Concrete Day 2010, in Rotterdam. Throughout the exhibition on November 18, SGS INTRON will present ... You can edit or delete your press release SGS INTRON Conducts Certification Services for TenCate Grass and Partners here. ... SGS INTRON Certificatie B.V.. Venusstraat 2, 4105 JH Culemborg. PO Box 267, 4100 AG Culemborg. The Netherlands. t: +31 (0)345 ...
This results in cleavage of the 3′ intron/exon junction and joining of the 5′ exon to the 3′ exon. The intron sequence (dark ... More importantly, the introns are spliced out and the exon sequences are fused to form the mature mRNA. This mRNA is then ... The cell must cleave the primary transcript at each end of the intron while holding on to the flanking exons so the chopped RNA ... In some cases, the introns can be thousands of nucleotides long-much longer than the exons.. Lets look at a simplified version ...
SimpleChIP® Human FKBP51 Intron 5 Primers contain a mix of forward and reverse PCR primers that are specific to the intron 5 ... SimpleChIP® Human FKBP51 Intron 5 Primers 7859. Toggle Between Dark and Light Modes Filter: *ChIP ... SimpleChIP® Human FKBP51 Intron 5 Primers were tested on DNA isolated from cross-linked cells using the SimpleChIP® Enzymatic ... SimpleChIP® Human FKBP51 Intron 5 Primers were tested on DNA isolated from cross-linked cells using the SimpleChIP® Enzymatic ...
Descubra todos los detalles y caracteristicas técnicas de Rudy Project Personal Protective Equipment Intron Guard ! ... Tralyx Guard e Intron son PPE de categoría 2. Las gafas PPE también cumplen con los estándares ANZI Z87 + pasando las pruebas ... Intron is the best value option in the PPE eyewear line. It combines lightness and stability while benefiting from the strength ...
Articles Citing PCMV-intron myc Rab11 S25N. <"clearfix">t data-page-length="10" data-b-auto-width="false"> Articles. TGFbeta ... PCMV-intron myc Rab11 S25N Citations (1). Plasmid Article: Seven transmembrane receptor core signaling complexes are assembled ...
Introns are also distinguished by phase, depending on where they occur relative to a codon. Phase 0 introns are found in ... As for the introns being fairly long, this also indirectly has to do with the signal peptide. In such proteins, the signal ... For one thing, introns enable alternative splicing. This refers to the selective joining of certain exons but not others. The ... It turned out that in most cases, the phase 1 introns in the group of genes in question resulted from the presence of a ...
Intron retention identifies a malaria vector within the Anopheles (Nyssorhynchus) albitaris complex (Diptera: Culicidae). ... 21Intron retention identifies a malaria vector within the Anopheles (Nyssorhynchus) albitaris complex (Diptera: Culicidae). ...
They] found lag times for splicing of 5-10 min for introns ranging from 1.2 kb to 240 kb. These times represent the time, after ... An unexpected finding of [researchers] study is that splicing occurred at a similar rate for several U2-dependent introns ... The splicing rates for small introns agree well with previous measurements (refs 19, 20). Note-the following 2 sources-[1] ...
All patients were first screened for the common intron 22 and intron 1 inversions. Inversion-negative samples were screened for ... Screening of mutations of hemophilia A in 40 Italian patients: a novel G-to-A mutation in intron 10 of the F8 gene as a ... In all patients with moderate and mild hemophilia A, a nucleotide change in the c.1538 -18G,A in intron 10, not reported in the ... These included five (12.5%) intron 22 inversions, one (2.5%) small deletion, one (2.5%) small insertion and seven (17.5%) point ...
90% of the mm6 introns could be ported to mm10 and matched with an intron. so in conclusion it can still be used, even though ... A new genome-wide search of minor introns has been performed and it led to the discovery of ~150 more minor introns (doi.org/ ... database minor introns • 1.5k views ADD COMMENT • link updated 7 months ago by Ram 37k • written 7.8 years ago by Martombo & ... and many of those introns dont really match with an intron of the most recent assembly (especially for the mouse genome). So ...
Ubi1 intron-mediated enhancement of the expression of Bt cry1Ah gene in transgenic maize (Zea mays L).pdf [ English. ] ... Intron-Mediated Enhancement- A Tool for Heterologous Gene Expression in Plants?.pdf [ English. ] ... Utilizing modified ubi1 introns to enhance exogenous gene expression in maize (Zea mays L.) and rice (Oryza sativa L.).pdf [ ...
... in the light of recent work on the molecular mechanisms regulating bacterial and phage group I and II intron dynamics, to show ... Group I and II introns can be considered as molecular parasites that interrupt protein-coding and structural RNA genes in all ... Group I and II introns can be considered as molecular parasites that interrupt protein-coding and structural RNA genes in all ... Learning to Live Together: Mutualism between Self-splicing Introns and Their Hosts ...
I am undergoing Intron-A treatment for hepatitis C. The nurse in charge of the treatment registry knows of no diet plan.. By ... I am undergoing INTRON-A treatment for Hepatitis C. One of the possible side effects of the treatment is suppression of the ... Home Immune Boosting I am undergoing Intron-A treatment for hepatitis C. The nurse in charge... ...
... has close relationship with intron. However, the relationship (if any) between SCUB and intron number as well as exon position ... To explore this relationship, the sequences of a set of genes containing between zero and nine introns was extracted from the ... These data provide some evidence of linkage between SCUB, the evolution of introns and DNA methylation, which brings about a ... was positively related to intron number, but that of NNA/NNT was inversely correlated; the opposite was the case in the land ...
It identifies intron-exon borders and splice sites and is able to cope with sequencing errors and genes spanning several ... it very often provides the user with the correct determination of intron-exon borders and splice sites, showing an improved ... From: Scipio: Using protein sequences to determine the precise exon/intron structures of genes and their orthologs in closely ...
The Acadian-specific 216G--,A mutation in exon 3 and a variant 9-repeat VNTR allele (designated VNTR(t,t)) in intron 5 are in ... The Acadian-specific 216GA mutation in exon 3 and a variant 9-repeat VNTR allele (designated VNTR(t,t)) in intron 5 are in ... Structure, diversity, and evolution of the 45-bp VNTR in intron 5 of the USH1C gene ... and evolution of the 45-bp VNTR in intron 5 of the USH1C gene. Genomics, 83 (3), 439-44. https://doi.org/10.1016/j.ygeno. ...
Sato M, Mori Y, Sakurada A, Fujimura S, Horii A. A GT dinucleotide repeat polymorphism in intron 1 of the H-cadherin (CDH13) ... A GT dinucleotide repeat polymorphism in intron 1 of the H-cadherin (CDH13) gene. In: Journal of Human Genetics. 1998 ; Vol. 43 ... Sato, M., Mori, Y., Sakurada, A., Fujimura, S., & Horii, A. (1998). A GT dinucleotide repeat polymorphism in intron 1 of the H- ... Sato, M, Mori, Y, Sakurada, A, Fujimura, S & Horii, A 1998, A GT dinucleotide repeat polymorphism in intron 1 of the H- ...
Huang M, Han Y, Zhang X, Pei F, Deng J, Kang J, Yan C. An intron polymorphism in the CXCL16 gene is associated with increased ... "Introns" is a descriptor in the National Library of Medicines controlled vocabulary thesaurus, MeSH (Medical Subject Headings) ... A Novel Regulatory Mechanism of Type II Collagen Expression via a SOX9-dependent Enhancer in Intron 6. J Biol Chem. 2017 Jan 13 ... This graph shows the total number of publications written about "Introns" by people in this website by year, and whether " ...
Retargeted intron targeting leuB gene in S. Agona. Lane 3: Retargeted intron targeting argD gene in S. Agona. (B) & (C) Intron ... leuB and argD metabolic gene knockout using group II intron technology. Group II intron technology was utilized to construct ... which resulted in a 350 bp retargeted intron. Lane 1: Retargeted intron targeting E.coli lacZ gene as positive control; Lane 2 ... C) Intron insertion in argD gene of S. Agona. Lane 20: PCR product of argD with targetron insertion (1,887 bp) in pure ...
Reactome is pathway database which provides intuitive bioinformatics tools for the visualisation, interpretation and analysis of pathway knowledge.
The first intron of the murine beta-casein gene contains a functional promoter. In: Biochemical and Biophysical Research ... The first intron of the murine beta-casein gene contains a functional promoter. Biochemical and Biophysical Research ... The first intron of the murine beta-casein gene contains a functional promoter. / Kolb, Andreas. ... Kolb, A. (2003). The first intron of the murine beta-casein gene contains a functional promoter. Biochemical and Biophysical ...
This is a list of changes made recently to pages linked from a specified page (or to members of a specified category). Pages on your watchlist are bold. ...
Roferon and Intron A differ from the natural product only in amino acid residue at position 23 and achieve similar results in ... Roferon and Intron A differ from the natural product only in amino acid residue at position 23 and achieve similar results in ...
Interferon alfa 2b (Interferon alfa-2b, Intron A). *View full drug information ...
Privacy & Cookies: This site uses cookies. By continuing to use this website, you agree to their use ...
  • The gene is transcribed from left (5′) to right (3′) beginning at the promoter (P). The long primary RNA transcript contains both intron and exon sequences. (blogspot.com)
  • More importantly, the introns are spliced out and the exon sequences are fused to form the mature mRNA. (blogspot.com)
  • This results in cleavage of the 3′ intron/exon junction and joining of the 5′ exon to the 3′ exon. (blogspot.com)
  • Another intron -enabled process important for gene evolution is exon shuffling. (medicalxpress.com)
  • The study reveals a clear and complete picture of how exon shuffling works and what role long phase 1 introns play in it. (medicalxpress.com)
  • Inversion-negative samples were screened for point mutations by direct sequencing of all coding regions and intron-exon boundaries of the factor 8 gene. (nih.gov)
  • The Acadian-specific 216G-->A mutation in exon 3 and a variant 9-repeat VNTR allele (designated VNTR(t,t)) in intron 5 are in complete linkage disequilibrium. (lsu.edu)
  • Introns are more important as like the exons, new gene or genotype combinations are constructed by introducing exon in new between or between unknown introns. (attainmfg.com)
  • After the 2'-OH of the A at the branch has joined to the initial G of the intron, the 3'‑OH of the upstream exon is available to react with the first nucleotide of the downstream exon, thereby joining the two exons via the phosphoester transfer mechanism. (dualjuridik.org)
  • Our results indicate that ORFs are efficiently captured without prior identification of intron-exon boundaries. (datadryad.org)
  • The nucleotide sequences of ten RHD exons and exon-intron boundary regions were evaluated by RHD gene-specific PCR-SSP and sequencing. (nih.gov)
  • A total of 31 PALB2 variants at the intron/exon boundaries were analyzed with MaxEntScan. (fecyt.es)
  • In both the species, diversity of microsatellites was highest in intergenic regions, followed by intron and exon regions, and lowest in coding regions. (who.int)
  • Challenging this assumption, a recent study has found a reduction in the mutation rate in exons compared to introns in somatic cells, ascribed to an enhanced exonic mismatch repair system activity. (nature.com)
  • After controlling for sampling bias in datasets with diseased probands and extended nucleotide context dependency, we find no reduction in the mutation rate in exons compared to introns in the germline. (nature.com)
  • A main requirement for the validation of this assumption is that mutation rate on exons and introns does not correlate with that sequence function. (nature.com)
  • 17 found in tumoral DNA, primarily from skin melanomas and DNA-polymerase- ε (POLE)-mutant colorectal cancers, that mutation rates are lower in exons than in introns after accounting for the trinucleotide-context-dependent mutational signature. (nature.com)
  • The study suggests that the lower mutation rate in exons results from an enhanced mismatch repair (MMR) activity in exons compared to introns. (nature.com)
  • In turn, the increased repair activity is attributed to different amounts of H3K36me3 epigenetic marks on exons and introns 17 . (nature.com)
  • The coding regions are divided into numerous blocks called "exons" and the exons are separated by "introns. (blogspot.com)
  • The triose phosphate isomerase (TPI) gene from maize is composed of 9 exons and 8 introns. (blogspot.com)
  • The cell must cleave the primary transcript at each end of the intron while holding on to the flanking exons so the chopped RNA transcript does not come apart. (blogspot.com)
  • In some cases, the introns can be thousands of nucleotides long-much longer than the exons. (blogspot.com)
  • Eukaryotic genes are composed of exons, which correspond to protein-coding sequences (ex-on signifies that they are expressed), and intervening sequences called introns (int-ron denotes their intervening role), which may be involved in gene regulation, but are removed from the pre-mRNA during processing.Intron sequences in mRNA do not encode functional proteins. (attainmfg.com)
  • The eukaryotic pre-mRNA possesses introns (intervening sequencing) that interrupt the exons (the coding regions). (attainmfg.com)
  • Introns and exons are parts of genes. (attainmfg.com)
  • Introns or the intervening sequence are considered as the non-coding part of the genes, while the exons or the expressed sequence are known to be as the coding part for proteins of the genes. (attainmfg.com)
  • Exons code for proteins, whereas introns do not. (attainmfg.com)
  • Eukaryotic cells possess a nucleus bound by a membrane, and their genes consist of alternating introns and exons. (attainmfg.com)
  • The pre-mRNA is cut, introns are spliced out (removed) and two flanking exons are joined together. (attainmfg.com)
  • For example, the human genome has groupings called introns and exons. (attainmfg.com)
  • A great way to remember this is by considering introns as intervening sequences and exons as expressed sequences. (attainmfg.com)
  • Introns are the common attribute found in the genes of the multicellular eukaryotes like humans, while exons are found in both prokaryotes and eukaryotes. (attainmfg.com)
  • Almost every gene has introns same introns are joined together therefore, the human genome has groupings called introns exons! (attainmfg.com)
  • Same introns introns were discovered in 1977 with the introduction of DNA sequencing introns as intervening sequences exons. (attainmfg.com)
  • Exons introns in prokaryotes expressed sequences eukaryotic cells possess a nucleus bound by a membrane, and their genes consist alternating! (attainmfg.com)
  • This post assumes you know what introns, exons and alternate splicing are. (wordpress.com)
  • know that RNA splicing occurs in molecular biology, and that it is a form of RNA processing in which a newly made precursor messenger RNA transcript is transformed into a mature messenger RNA (mRNA): During splicing introns are removed and exons arejoined together, but what would happen if the introns were not removed? (solvedlib.com)
  • In the second step, the 3' splice site is cleaved and the exons are fused with concomitant release of the intron lariat. (bdbiosciences.com)
  • Namely, genes contain noncoding regions referred to as introns. (medicalxpress.com)
  • To their surprise, the study's authors identified a group of genes containing an unusually large number of phase 1 introns that were over 50,000 nucleotide pairs long. (medicalxpress.com)
  • It turned out that in most cases, the phase 1 introns in the group of genes in question resulted from the presence of a particular amino acid sequence at the beginning of the protein. (medicalxpress.com)
  • Group I and II introns can be considered as molecular parasites that interrupt protein-coding and structural RNA genes in all domains of life. (uwo.ca)
  • Some introns code for separate genes. (rush.edu)
  • Transcriptional enhancer elements are found in the 5' upstream regions of casein genes but have also been detected in the first intron of the bovine beta-casein gene. (elsevier.com)
  • Introns are interruptions in the text of eukaryotic genes. (attainmfg.com)
  • Cut, introns are interruptions in the text of eukaryotic genes are also present in prokaryotes but removed entirely make. (attainmfg.com)
  • Three genes of T4 phage were found to have stretches of non-coding sequences which belonged to the group IA type introns of self-splicing nature. (who.int)
  • Just how widespread this is, isn't known, but most protein coding genes have introns. (wordpress.com)
  • It is now safe to assume that any gene containing introns (95% of all protein coding genes [ Proc. (wordpress.com)
  • An intron characteristic of Archaeal tRNA and rRNA genes, where intron transcript generates a bulge-helix-bulge motif that is recognised by a splicing endoribonuclease. (virtualflybrain.org)
  • Intron numbers of SbSOD genes ranged from 5 to 7. (tubitak.gov.tr)
  • Secuencias de ADN en los genes que se localizan entre los EXONES. (bvsalud.org)
  • Learning to Live Together: Mutualism between Self-splicing Introns and" by David R. Edgell, Venkata R. Chalamcharla et al. (uwo.ca)
  • IMSEAR at SEARO: A unique group of self-splicing introns in bacteriophage T4. (who.int)
  • Khan AU, Ajamaluddin M, Ahmad M. A unique group of self-splicing introns in bacteriophage T4. (who.int)
  • The currently available full-genome sequences of many organisms have made it possible to study the evolution of introns in detail. (medicalxpress.com)
  • And it is precisely there, at the beginning of a gene, that long introns tend to occur, because they contain regulatory DNA sequences important for the protein's synthesis. (medicalxpress.com)
  • Moss, Stephen P., Domino A. Joyce, Stuart Humphries, Katherine J. Tindall and David H. Lunt (2011) Comparative analysis of teleost genome sequences reveals an ancient intron size expansion in the zebrafish lineage. (davelunt.net)
  • Huang M, Han Y, Zhang X, Pei F, Deng J, Kang J, Yan C. An intron polymorphism in the CXCL16 gene is associated with increased risk of coronary artery disease in Chinese Han population: a large angiography-based study. (rush.edu)
  • GU is invariant at the 5' splice site, and AG is (almost) invariant at the 3' splice site for the most prevalent class of introns in pre-mRNA. (dualjuridik.org)
  • Together with an analysis of intron length and splice site strength, we observe that the genomic signature of splicing-coupled selection differs between long and short introns . (bvsalud.org)
  • and many of those introns don't really match with an intron of the most recent assembly (especially for the mouse genome). (biostars.org)
  • A new genome-wide search of minor introns has been performed and it led to the discovery of ~150 more minor introns ( doi.org/10.1186/s12864-019-6046-x ). (biostars.org)
  • Introns are very much common in the genome of higher vertebrates such as human beings, mammals, amphibians, fish and mice but unlikely to be seen in the genome of certain varieties of eukaryotic micro-organism. (attainmfg.com)
  • I am always a bit frustrated with the way introns are treated in many genome characterisation papers- "the genome contained Y introns with mean intron. (davelunt.net)
  • Intron endonucleases and inteins attract considerable attention for their molecular mechanisms, phylogenetic diversity, role in genome evolution, and application in research, biotechnology and medicine. (grantome.com)
  • Understanding the function of noncoding regions in the genome , such as introns , is of central importance to evolutionary biology . (bvsalud.org)
  • Splicing, the removal of introns from pre-mRNA, is mediated by spliceosomal complexes and occurs in two distinct catalytic steps. (bdbiosciences.com)
  • The genomic signature of splicing-coupled selection differs between long and short introns. (bvsalud.org)
  • On one hand , the sequence of introns , especially short introns , appears to evolve in an almost neutral manner. (bvsalud.org)
  • The strongest signal we identify is associated with short introns . (bvsalud.org)
  • The intron sequence (dark brown) is released as a lariat (looped) structure. (blogspot.com)
  • Intron lariat is the equivalent of a "circular" intermediate. (dualjuridik.org)
  • The nuclear group I introns, exemplified by the rRNA introns of Tetrahymena thermophila and Physarum polycephalum, may well have arisen by â ¦ And eukaryotes evolving from these early ancestors should keep some of these same introns. (attainmfg.com)
  • Three types of man-made cytokines have been approved to treat melanoma skin cancer: interferon alfa-2b (Intron A), pegylated interferon alfa-2b (Sylatron), and interleukin-2 (aldesleukin, Proleukin). (healthline.com)
  • Introns are also distinguished by phase, depending on where they occur relative to a codon. (medicalxpress.com)
  • Phase 0 introns are found in between codons, whereas phases 1 and 2 occur immediately after the first or second nucleotide in the codon, respectively. (medicalxpress.com)
  • P53 haplotypes defined by 3 polymorphisms (codon 72, intron 3, and intron 6) have been implicated in breast cancer]. (cdc.gov)
  • This endonuclease recognizes a long DNA site approximately 20 base pairs in length and facilitates the lateral transfer of that intron. (rcsb.org)
  • First, we showed that phage T4 group I intron endonuclease 1-Tevl, a member of the GIY-YIG family, is bifunctional, doubling as a transcriptional autorepressor. (grantome.com)
  • Second, we engineered the archaeal l-Dmol intron endonuclease, a monomeric LAGLIDADG family enzyme, into a heterodimer, a homodimer and a monomer with altered specificity, an accomplishment with both practical and evolutionary implication. (grantome.com)
  • Third, we caught a first glimpse, by cryo-electron microscopy (EM), of a lactococcal group II intron-encoded retroelement, consisting of the protein which has endonuclease and reverse transcriptase (RT) activity, in complex with its intron RNA, scaffolded on a ribosome. (grantome.com)
  • For one thing, introns enable alternative splicing. (medicalxpress.com)
  • An unexpected finding of [researchers'] study is that splicing occurred at a similar rate for several U2-dependent introns spanning a wide range of sizes. (harvard.edu)
  • They] found lag times for splicing of 5-10 min for introns ranging from 1.2 kb to 240 kb. (harvard.edu)
  • The splicing rates for small introns agree well with previous measurements (refs 19, 20). (harvard.edu)
  • Introns may therefore be under pressure to maintain their self-splicing character in prokaryotes. (attainmfg.com)
  • We describe in this review, the salient splicing features of group I introns of bacteriophage T4 and propose, a hypothetical model to fit in the self-splicing of nrdB intron of T4 phage. (who.int)
  • Therefore, T4 bacteriophage can serve as a good model system to study the evolutionary aspects of splicing of introns. (who.int)
  • The 2'‑OH of an A at the "branch" point forms a phosphoester with the first G of the intron to initiate splicing. (dualjuridik.org)
  • The conserved LAGLIDADG motif, which is found in many mobile intron endonucleases, maturases and inteins, forms a novel helical interface and contributes essential residues to the active site. (rcsb.org)
  • Homing endonucleases are rare-cutting DNA cleavage enzymes that are most often encoded by introns and inteins. (grantome.com)
  • Once considered purely selfish DNA elements, they now seem, in the light of recent work on the molecular mechanisms regulating bacterial and phage group I and II intron dynamics, to show evidence of co-evolution with their hosts. (uwo.ca)
  • A in intron 10, not reported in the HAMSTeRS factor 8 mutation database (http://europium.csc.mrc.ac.uk/), was found. (nih.gov)
  • If this reduction happens also in the germline, it can compromise studies of population genomics, including the detection of selection when using introns as proxies for neutrality. (nature.com)
  • If you are taking INTRON A with REBETOL, also read the Medication Guide for REBETOL ® (ribavirin) Capsules and Oral Solution. (nih.gov)
  • The various components of the spliceosome have to assemble at the 5′ (left) end of an intron and at the 3′ end. (blogspot.com)
  • First, transcriptional enhancer elements present in the intron increase the basal activity of the beta-casein promoter. (elsevier.com)
  • A snippet of RNA from an intron in a gene can bind to an upstream regulatory element forming a triple helix and shut off transcription of the gene. (wordpress.com)
  • Now a team of bioinformaticians from MIPT and IMPB RAS has examined the relation between intron phase and length in humans and mice. (medicalxpress.com)
  • I'm interested in studying minor introns in both humans and mice. (biostars.org)
  • To probe the structure and function of the l-TevI linker, which serves as a communication bridge between catalytic and DNA binding domains and controls cleavage versus repression;and to test the hypothesis that the linker acts as a redox switch, that regulates cleavage fidelity and thereby influences intron spread. (grantome.com)
  • INTRON A alone is a treatment for certain types of cancers and hepatitis B virus. (nih.gov)
  • INTRON A by itself or with REBETOL is a treatment for some people infected with hepatitis C virus. (nih.gov)
  • I am undergoing Intron-A treatment for hepatitis C. The nurse in charge of the treatment registry knows of no diet plan. (dietitian.com)
  • Home Immune Boosting I am undergoing Intron-A treatment for hepatitis C. The nurse in charge. (dietitian.com)
  • I am undergoing INTRON-A treatment for Hepatitis C . One of the possible side effects of the treatment is suppression of the bone marrow"s ability to produce blood cells. (dietitian.com)
  • Introns" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus, MeSH (Medical Subject Headings) . (rush.edu)
  • 2. To use cryo-EM, among other techniques, to lay the structural foundation for biochemical function of the group II intron ribonucleoprotein (RNP), and study RNP interactions with target DNA in the tri-macromolecular initiation complex for retromobility. (grantome.com)
  • A Novel Regulatory Mechanism of Type II Collagen Expression via a SOX9-dependent Enhancer in Intron 6. (rush.edu)
  • Of the 40 patients, 20 (50%) had severe hemophilia A, 19 (47.5%) had moderate hemophilia A, and one (2.5%) had mild hemophilia A. All patients were first screened for the common intron 22 and intron 1 inversions. (nih.gov)
  • Intron 22 inversion (inv22) may account for 45% of all cases of severe haemophilia A. Haemophilia A is underdiagnosed in South Africa (SA), and owing to limited resources the genotypes of most haemophilia A patients are unknown.Objectives. (bvsalud.org)
  • Nous avons génotypé les deux polymorphismes mononucléotidiques du gène ADIPOQ chez 140 patients atteints de DNID sans lien de parenté et 66 témoins non diabétiques en recourant à l'analyse du polymorphisme de longueur des fragments de restriction par réaction en chaîne de polymérase. (who.int)
  • Structure, diversity, and evolution of the 45-bp VNTR in intron 5 of t" by Sevtap Savas, Ben Frischhertz et al. (lsu.edu)
  • I have a project going at the moment to examine changes in intron diversity, size and location in animal genomes. (davelunt.net)
  • These included five (12.5%) intron 22 inversions, one (2.5%) small deletion, one (2.5%) small insertion and seven (17.5%) point mutations. (nih.gov)
  • We have used a method based on DNA strand asymmetery that does not require comparison with any putatively neutrally evolving sequence, nor sequence conservation between species, to detect selection within introns . (bvsalud.org)
  • With a team of highly experienced experts, SGS INTRON tested the synthetic turf components and systems in accordance with the field of application and standards established by sports associations. (openpr.com)
  • High level transcription of the complement regulatory protein CD59 requires an enhancer located in intron 1. (ox.ac.uk)
  • Intron-Mediated Enhancement- A Tool for Heterologous Gene Expression in Plants? (cbd.int)
  • However, within the cells of multicelled animals and plants almost every gene has introns. (attainmfg.com)
  • Kolb, A 2003, ' The first intron of the murine beta-casein gene contains a functional promoter ', Biochemical and Biophysical Research Communications , vol. 306, no. 4, pp. 1099-1105. (elsevier.com)