DNA-Directed RNA Polymerases
RNA
RNA Polymerase I
DNA-Directed DNA Polymerase
RNA Polymerase II
RNA Polymerase III
Amanitins
Templates, Genetic
RNA, Small Interfering
RNA Replicase
Transcription, Genetic
Molecular Sequence Data
Base Sequence
RNA, Ribosomal
DNA Polymerase I
RNA Editing
DNA Polymerase II
RNA Splicing
Amino Acid Sequence
Bacteriophage T7
RNA, Bacterial
Escherichia coli
RNA, Double-Stranded
DNA
DNA Polymerase III
RNA, Messenger
Saccharomyces cerevisiae
RNA Interference
Nucleic Acid Conformation
Cell Nucleus
Bacteriophage T3
RNA, Fungal
Mutation
Promoter Regions, Genetic
DNA Polymerase beta
Nucleotides
Models, Molecular
TATA-Box Binding Protein
Binding Sites
Alpha-Amanitin
RNA, Plant
RNA, Small Nuclear
RNA, Transfer
Manganese
Thermus
Catalytic Domain
HeLa Cells
RNA, Catalytic
Sequence Homology, Amino Acid
Bacteriophage N4
Eukaryotic Cells
RNA Processing, Post-Transcriptional
Conserved Sequence
Base Pairing
RNA Nucleotidyltransferases
Cell Nucleolus
Taq Polymerase
Deoxyribonucleotides
RNA-Directed DNA Polymerase
Sequence Alignment
Protein Binding
Substrate Specificity
Macromolecular Substances
Protein Subunits
Transcription Factors
RNA, Antisense
Saccharomyces cerevisiae Proteins
Plasmids
RNA Stability
T-Phages
Transcriptional Elongation Factors
DNA Repair
Magnesium
Protein Structure, Tertiary
Thymine Nucleotides
Virus Replication
Polydeoxyribonucleotides
Polynucleotide Adenylyltransferase
DNA Primers
RNA Precursors
Allolevivirus
Chromatin
Uridine Triphosphate
RNA, Untranslated
Nucleic Acid Hybridization
Sequence Homology, Nucleic Acid
Archaea
Proliferating Cell Nuclear Antigen
Exonucleases
Mutagenesis
RNA, Archaeal
RNA Caps
Oligonucleotides
Protein Conformation
Sequence Analysis, RNA
Models, Genetic
Cloning, Molecular
DNA Damage
DNA, Single-Stranded
Prokaryotic Cells
Chromatography, DEAE-Cellulose
Genes
Transcription Factors, General
Poly dA-dT
Centrifugation, Density Gradient
Cytidine Triphosphate
Structure-Activity Relationship
Aphidicolin
DNA Nucleotidyltransferases
Transcription Factor TFIIB
Dactinomycin
Sigma Factor
Hydroxyacetylaminofluorene
DNA Primase
Temperature
Bacteriophage phi 6
Evolution, Molecular
Crystallography, X-Ray
RNA-Binding Proteins
Mutagenesis, Site-Directed
RNA, Protozoan
Species Specificity
Potassium Permanganate
DNA-Binding Proteins
Protein Biosynthesis
Salmon
Holoenzymes
rRNA Operon
Gene Silencing
Cytidine Monophosphate
Transcription Termination, Genetic
TATA Box
Chromatography, Ion Exchange
Catalysis
Arabidopsis
Poliovirus
Eukaryota
Ribonucleotides
Carmovirus
Rifampin
Electrophoresis, Polyacrylamide Gel
RNA Ligase (ATP)
Amino Acid Motifs
Cell-Free System
Poly(ADP-ribose) Polymerases
DNA, Ribosomal
Yeasts
Pol1 Transcription Initiation Complex Proteins
Cattle
Transcription Factor TFIIIB
Chloroplasts
DEAD-box RNA Helicases
Open Reading Frames
Sulfolobus solfataricus
Bromovirus
Plasmacytoma
Recombinant Fusion Proteins
Oligodeoxyribonucleotides
Polymerase Chain Reaction
Thymus Gland
Plastids
Exodeoxyribonucleases
In vivo and in vitro processing of the Bacillus subtilis transcript coding for glutamyl-tRNA synthetase, serine acetyltransferase, and cysteinyl-tRNA synthetase. (1/6307)
In Bacillus subtilis, the adjacent genes gltX, cysE, and cysS encoding respectively glutamyl-tRNA synthetase, serine acetyl-transferase, and cysteinyl-tRNA synthetase, are transcribed as an operon but a gltX probe reveals only the presence of a monocistronic gltX mRNA (Gagnon et al., 1994, J Biol Chem 269:7473-7482). The transcript of the gltX-cysE intergenic region contains putative alternative secondary structures forming a p-independent terminator or an antiterminator, and a conserved sequence (T-box) found in the leader of most aminoacyl-tRNA synthetase and many amino acid biosynthesis genes in B. subtilis and in other Gram-positive eubacteria. The transcription of these genes is initiated 45 nt upstream from the first codon of gltX and is under the control of a sigmaA-type promoter. Analysis of the in vivo transcript of this operon revealed a cleavage site immediately downstream from the p-independent terminator structure. In vitro transcription analysis, using RNA polymerases from Escherichia coli, B. subtilis, and that encoded by the T7 phage, in the presence of various RNase inhibitors, shows the same cleavage. This processing generates mRNAs whose 5'-end half-lives differ by a factor of 2 in rich medium, and leaves putative secondary structures at the 3' end of the gltX transcript and at the 5' end of the cysE/S mRNA, which may be involved in the stabilization of these mRNAs. By its mechanism and its position, this cleavage differs from that of the other known transcripts encoding aminoacyl-tRNA synthetases in B. subtilis. (+info)Autoantibodies to RNA polymerases recognize multiple subunits and demonstrate cross-reactivity with RNA polymerase complexes. (2/6307)
OBJECTIVE: To determine the subunit specificity of autoantibody directed to RNA polymerases (RNAP) I, II, and III, which is one of the major autoantibody responses in patients with systemic sclerosis (SSc). METHODS: Thirty-two SSc sera with anti-RNAP antibodies (23 with anti-RNAP I/III, 5 with anti-RNAP I/III and II, and 4 with anti-RNAP II alone) were analyzed by immunoblotting using affinity-purified RNAP and by immunoprecipitation using 35S-labeled cell extracts in which RNAP complexes were dissociated. Antibodies bound to individual RNAP subunits were eluted from preparative immunoblots and were further analyzed by immunoblotting and immunoprecipitation. RESULTS: At least 15 different proteins were bound by antibodies in anti-RNAP-positive SSc sera in various combinations. All 9 sera immunoprecipitating RNAP II and all 28 sera immunoprecipitating RNAP I/III recognized the large subunit proteins of RNAP II and III, respectively. Reactivity to RNAP I large subunits was strongly associated with bright nucleolar staining by indirect immunofluorescence. Affinity-purified antibodies that recognized a 62-kd subunit protein cross-reacted with a 43-kd subunit protein and immunoprecipitated both RNAP I and RNAP III. Antibodies that recognized a 21-kd subunit protein obtained from sera that were positive for anti-RNAP I/III and II antibodies immunoprecipitated both RNAP II and RNAP III. CONCLUSION: Anti-RNAP antibodies recognize multiple subunits of RNAP I, II, and III. Moreover, the results of this study provide the first direct evidence that antibodies that recognize shared subunits of human RNAPs or epitopes present on different human RNAP subunits are responsible for the recognition of multiple RNAPs by SSc sera. (+info)Efficient synthesis of nucleic acids heavily modified with non-canonical ribose 2'-groups using a mutantT7 RNA polymerase (RNAP). (3/6307)
A T7 RNAP mutant (Y639F) which eliminates discrimination of the chemical character of the NTP ribose 2'-group, facilitates incorporation of non-canonicalsubstrates into nucleic acids. However, transcripts containing a high percentage of non-canonical NMPs are poorly extended due to effects of the 2'-substituents on the transcript:template hybrid conformation. We tested the addition of compounds that stabilize A-type helix geometry to the reaction. High concentrations of polyamines, together with other changes in reaction conditions, greatly increased the synthesis of transcripts heavily substituted with non-canonical ribose 2'-groups. Template structures that facilitate promoter opening increased the efficiency of reactions where non-canonical substrates were incorporated during transcription of +1 to +6. (+info)General method of analysis of kinetic equations for multistep reversible mechanisms in the single-exponential regime: application to kinetics of open complex formation between Esigma70 RNA polymerase and lambdaP(R) promoter DNA. (4/6307)
A novel analytical method based on the exact solution of equations of kinetics of unbranched first- and pseudofirst-order mechanisms is developed for application to the process of Esigma70 RNA polymerase (R)-lambdaPR promoter (P) open complex formation, which is described by the minimal three-step mechanism with two kinetically significant intermediates (I1, I2), [equation: see text], where the final product is an open complex RPo. The kinetics of reversible and irreversible association (pseudofirst order, [R] >> [P]) to form long-lived complexes (RPo and I2) and the kinetics of dissociation of long-lived complexes both exhibit single exponential behavior. In this situation, the analytical method provides explicit expressions relating observed rate constants to the microscopic rate constants of mechanism steps without use of rapid equilibrium or steady-state approximations, and thereby provides a basis for interpreting the composite rate constants of association (ka), isomerization (ki), and dissociation (kd) obtained from experiment for this or any other sequential mechanism of any number of steps. In subsequent papers, we apply this formalism to analyze kinetic data obtained in the reversible and irreversible binding regimes of Esigma70 RNA polymerase (R)-lambdaP(R) promoter (P) open complex formation. (+info)The Escherichia coli Ada protein can interact with two distinct determinants in the sigma70 subunit of RNA polymerase according to promoter architecture: identification of the target of Ada activation at the alkA promoter. (5/6307)
The methylated form of the Ada protein (meAda) activates transcription from the Escherichia coli ada, aidB, and alkA promoters with different mechanisms. In this study we identify amino acid substitutions in region 4 of the RNA polymerase subunit sigma70 that affect Ada-activated transcription at alkA. Substitution to alanine of residues K593, K597, and R603 in sigma70 region 4 results in decreased Ada-dependent binding of RNA polymerase to the alkA promoter in vitro and impairs alkA transcription both in vivo and in vitro, suggesting that these residues define a determinant for meAda-sigma70 interaction. In a previous study (P. Landini, J. A. Bown, M. R. Volkert, and S. J. W. Busby, J. Biol. Chem. 273:13307-13312, 1998), we showed that a set of negatively charged amino acids in sigma70 region 4 is involved in meAda-sigma70 interaction at the ada and aidB promoters. However, the alanine substitutions of positively charged residues K593, K597, and R603 do not affect meAda-dependent transcription at ada and aidB. Unlike the sigma70 amino acids involved in the interaction with meAda at the ada and aidB promoters, K593, K597, and R603 are not conserved in sigmaS, an alternative sigma subunit of RNA polymerase mainly expressed during the stationary phase of growth. While meAda is able to promote transcription by the sigmaS form of RNA polymerase (EsigmaS) at ada and aidB, it fails to do so at alkA. We propose that meAda can activate transcription at different promoters by contacting distinct determinants in sigma70 region 4 in a manner dependent on the location of the Ada binding site. (+info)An intrinsic DNA curvature found in the cyanobacterium Microcystis aeruginosa K-81 affects the promoter activity of rpoD1 encoding a principal sigma factor. (6/6307)
The rpoD1 gene in the unicellular cyanobacterium Microcystis aeruginosa K-81 encodes a principal sigma factor of RNA polymerase and is transcribed under light and dark conditions to produce multiple monocistronic transcripts. In the 5'-upstream region from rpoD1 Promoter 2, which has a sequence of Escherichia coli type, we found a sequence-directed DNA curvature with an AT-rich sequence. Insertions of 2 to 21 base pairs introduced into the curved center changed a gross geometry of the original curved DNA structure. The rpoD1 promoter activities assayed in vivo by using transcriptional lacZ fusions were correlated with the change in the gross geometry in not only a cyanobacterium but also E. coli. In addition, RNA polymerase binding to the rpoD1 promoter region and the efficiency of the mRNA synthesis from the rpoD1 Promoter 2 were also affected in vitro by the change in the geometry. These results suggest that the tertiary structure of the curved DNA is important for the rpoD1 transcription. The deletion of the center region of the curvature resulted in a considerable reduction of the transcription from Promoter 2 in the cyanobacterium. This report demonstrates that a curved DNA plays a significant role in transcription in cyanobacteria, and that this functional curvature is located in the 5'-upstream region from the rpoD gene, which encodes a principal sigma factor in eubacteria. (+info)Disruption of substrate binding site in E. coli RNA polymerase by lethal alanine substitutions in carboxy terminal domain of the beta subunit. (7/6307)
Alanine substitution of four amino acids in two evolutionarily conserved motifs, PSRM and RFGEMIE, near the carboxy terminus of the beta subunit of E. coli RNA polymerase results in a dramatic loss of the enzyme's affinity to substrates with no apparent effect on the maximal rate of the enzymatic reaction or on binding to promoters. The magnitude and selectivity of the effect suggest that the mutations disrupt the substrate binding site of the active center. (+info)Bone marrow ribonucleic acid polymerase. Effect of testosterone on nucleotide incorporation into nuclear RNA. (8/6307)
The incorporation of 3H-UTP into RNA by isolated rat bone marrow nuclei is stimulated by testosterone. This effect is hormone and tissue specific. Using alpha-amanitine and different ionic strength conditions it was found that testosterone enhances preferentially RNA polymerase I activity. The sedimentation pattern of RNA isolated from bone marrow nuclei shows that the synthesis of RNA species within the 14-30 S range is mainly stimulated by the hormone. (+info)Plasmacytoma is a type of plasma cell dyscrasia, which is a group of diseases that affect the production and function of plasma cells. Plasma cells are a type of white blood cell that produces antibodies to fight infections. In plasmacytoma, the abnormal plasma cells grow and multiply out of control, leading to a tumor.
There are several subtypes of plasmacytoma, including:
* solitary plasmacytoma: A single tumor that occurs in one location.
* multiple myeloma: A type of cancer that affects the bones and is characterized by an overgrowth of malignant plasma cells in the bone marrow.
* extramedullary plasmacytoma: A tumor that occurs outside of the bone marrow, such as in soft tissue or organs.
Plasmacytoma is usually diagnosed through a combination of physical examination, imaging tests such as X-rays or CT scans, and biopsy. Treatment typically involves chemotherapy and/or radiation therapy to destroy the abnormal cells. In some cases, surgery may be necessary to remove the tumor.
Plasmacytoma is a relatively rare cancer, but it can be aggressive and potentially life-threatening if left untreated. It is important for patients with symptoms of plasmacytoma to seek medical attention as soon as possible to receive an accurate diagnosis and appropriate treatment.
The signs and symptoms of CE can vary depending on the location of the tumor, but they may include:
* Lumps or swelling in the neck, underarm, or groin area
* Fever
* Fatigue
* Weight loss
* Night sweats
* Swollen lymph nodes
* Pain in the affected area
CE is caused by a genetic mutation that leads to uncontrolled cell growth and division. The exact cause of the mutation is not fully understood, but it is believed to be linked to exposure to certain viruses or chemicals.
Diagnosis of CE typically involves a combination of physical examination, imaging tests such as CT scans or PET scans, and biopsy to confirm the presence of cancer cells. Treatment options for CE depend on the stage and location of the tumor, but may include:
* Chemotherapy to kill cancer cells
* Radiation therapy to shrink the tumor
* Surgery to remove the tumor
* Immunotherapy to boost the immune system's ability to fight the cancer
Overall, CE is a rare and aggressive form of cancer that requires prompt diagnosis and treatment to improve outcomes.
1. Influenza (flu): Caused by the influenza virus, which is an RNA virus that affects the respiratory system and can cause fever, cough, sore throat, and body aches.
2. HIV/AIDS: Caused by the human immunodeficiency virus (HIV), which is an RNA virus that attacks the body's immune system and can lead to acquired immunodeficiency syndrome (AIDS).
3. Hepatitis B: Caused by the hepatitis B virus, which is an RNA virus that infects the liver and can cause inflammation, scarring, and cancer.
4. Measles: Caused by the measles virus, which is an RNA virus that affects the respiratory system and can cause fever, cough, and a rash.
5. Rabies: Caused by the rabies virus, which is an RNA virus that attacks the central nervous system and can cause brain damage and death.
6. Ebola: Caused by the Ebola virus, which is an RNA virus that affects the blood vessels and can cause fever, vomiting, diarrhea, and bleeding.
7. SARS-CoV-2: Caused by the severe acute respiratory syndrome-related coronavirus 2 (SARS-CoV-2), which is an RNA virus that affects the respiratory system and can cause COVID-19.
RNA virus infections are often difficult to treat and can be highly contagious, so it's important to take precautions to prevent transmission and seek medical attention if symptoms persist or worsen over time.
There are two main types of systemic scleroderma: diffuse cutaneous systemic sclerosis (DCSS) and limited cutaneous systemic sclerosis (LCSS). DCSS is characterized by skin thickening and scar formation over the trunk, arms, and legs, while LCSS is characterized by skin tightening and patches of scaly skin on the hands and face.
The symptoms of systemic scleroderma can include:
* Skin hardening and tightening
* Fatigue
* Joint pain and stiffness
* Muscle weakness
* Swallowing difficulties
* Heartburn and acid reflux
* Shortness of breath
* Raynaud's phenomenon (pale or blue-colored fingers and toes in response to cold temperatures or stress)
The exact cause of systemic scleroderma is not known, but it is believed to involve a combination of genetic and environmental factors. Treatment options for systemic scleroderma include medications to manage symptoms such as pain, stiffness, and swallowing difficulties, as well as physical therapy and lifestyle modifications to improve quality of life.
In summary, systemic scleroderma is a chronic autoimmune disease that affects multiple systems in the body, causing skin hardening and thickening, fatigue, joint pain, and other symptoms. While there is no cure for systemic scleroderma, treatment options are available to manage symptoms and improve quality of life.
There are several types of genomic instability, including:
1. Chromosomal instability (CIN): This refers to changes in the number or structure of chromosomes, such as aneuploidy (having an abnormal number of chromosomes) or translocations (the movement of genetic material between chromosomes).
2. Point mutations: These are changes in a single base pair in the DNA sequence.
3. Insertions and deletions: These are changes in the number of base pairs in the DNA sequence, resulting in the insertion or deletion of one or more base pairs.
4. Genomic rearrangements: These are changes in the structure of the genome, such as chromosomal breaks and reunions, or the movement of genetic material between chromosomes.
Genomic instability can arise from a variety of sources, including environmental factors, errors during DNA replication and repair, and genetic mutations. It is often associated with cancer, as cancer cells have high levels of genomic instability, which can lead to the development of resistance to chemotherapy and radiation therapy.
Research into genomic instability has led to a greater understanding of the mechanisms underlying cancer and other diseases, and has also spurred the development of new therapeutic strategies, such as targeted therapies and immunotherapies.
In summary, genomic instability is a key feature of cancer cells and is associated with various diseases, including cancer, neurodegenerative disorders, and aging. It can arise from a variety of sources and is the subject of ongoing research in the field of molecular biology.
RNA polymerase IV
RNA polymerase II subunit B4
RNA-polymerase)-subunit kinase
POLR3D
POLR3E
POLR2C
POLRMT
RNA polymerase II holoenzyme
POLR2K
Viral eukaryogenesis
POLR3G
Wiedemann-Rautenstrauch syndrome
POLR2B
POLR2E
POLR2A
POLR2I
POLR2L
POLR3F
POLR2J
POLR2H
POLR3K
POLR2J2
Maurice Green (virologist)
Alan Ming-ta Wu
Rauchvirus
ZNRD1
POLR1A
POLR2G
Grapevine virus A
DNA polymerase mu
Sulfolobus
CDC25C
Promoter (genetics)
Michal Hocek
Short interspersed nuclear element
Glucocorticoid receptor
Enzyme inhibitor
Eggerthellaceae
ENDOG
Environmental DNA
Index of biochemistry articles
Nuclear receptor
Orthohantavirus
POLE (gene)
Picornavirus
No-SCAR (Scarless Cas9 Assisted Recombineering) Genome Editing
Chromosome 16
Epigenomics
Artificial transcription factor
Transcription factor II B
RBBP8
STAT6
Telomerase RNA component
Cdc14
Viroid
Psoralen
Ligand binding assay
Ubiquitin
DNA-directed RNA polymerase subunit omega(rpoZ) | Technique alternative | 01023070510 - Scetibio
6vyt.10 | SWISS-MODEL Template Library
Sigma70 promoters in Escherichia coli: specific transcription in dense regions of overlapping promoter-like signals
SCOPe 2.07: Domain d1hqmb : 1hqm B
Browsing Journal Articles by Subject
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MPD: Genes and genomic regions
HIV Reverse Transcriptase | Profiles RNS
YRC Public Data Repository - Protein Structure Prediction - Protein Overview
PCR Amplification | An Introduction to PCR Methods | Promega
Nutrients | Free Full-Text | Towards an Integrative Understanding of tRNA Aminoacylation-Diet-Host-Gut Microbiome Interactions...
DeCS
Removal of double-stranded contaminants from RNA transcripts: Synthesis of adenovirus VA RNA|sub|1|/sub| from a T7 vector -...
Error rate in transcription with the wild typ - Eukaryotes - BNID 111573
Neonatal avian pneumovirus infection in commercial turkeys - Fingerprint
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MECHANISMS OF COOPERATIVE PROTEIN-DNA INTERACTIONS
- Albert Einstein College of Medicine
Purifying selection masks the mutational flexibility of HIV-1 reverse transcriptase<...
The invasive MED/Q Bemisia tabaci genome: a tale of gene loss and gene gain | BMC Genomics | Full Text
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SMED30021552
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General transcription factor specified global gene regulation in archaea - Fingerprint - NYU Scholars
Mechanism of Ribonucleic Acid Chain Initiation. 1. A Non-Steady-State Study of Ribonucleic Acid Synthesis Without Enzyme...
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Pesquisa | Portal Regional da BVS
Proteins6
- The goal of the proposed biophysical studies is to understand the physical mechanisms by which cooperative DNA-binding proteins regulate the transcription of genes. (elsevier.com)
- This method is unique in that it allows resolution of both the intrinsic and cooperative Gibbs free energies for proteins which bind to multiple, specific-sites on DNA. (elsevier.com)
- Ribosomal RNA and transfer RNA assemble protein building blocks (amino acids) into functioning proteins, which is essential for the normal functioning and survival of cells. (medlineplus.gov)
- Cells depend on their DNA for coding information to make various classes of proteins that include enzymes, certain hormones, transport proteins, and structural proteins that support life. (cdc.gov)
- Specialized cell structures called ribosomes are the cellular organelles that actually synthesize the proteins (RNA transcription). (cdc.gov)
- RNA, lipids, and proteins. (who.int)
Ribosomal2
- The MTD test uses transcription-mediated amplification to detect M. tuberculosis-complex ribosomal RNA (2). (cdc.gov)
- Both enzymes help synthesize a form of RNA known as ribosomal RNA (rRNA). (medlineplus.gov)
Synthesis4
- RNA synthesis is central to life, and RNA polymerase (RNAP) depends on accessory factors for recovery from stalled states and adaptation to environmental changes. (nih.gov)
- p.6 left column paragraph above bottom paragraph:'The error rate in transcription with the wild type trigger loop is on the order of 10^- 6, of which about 10^- 4 may be accounted for by the fidelity of RNA synthesis. (harvard.edu)
- These enzymes are involved in the production (synthesis) of ribonucleic acid (RNA), a chemical cousin of DNA. (medlineplus.gov)
- RNA polymerase III also plays a role in the synthesis of several other forms of RNA, including transfer RNA (tRNA). (medlineplus.gov)
Protein3
- DNA-directed RNA polymerase subunit omega(rpoZ) is a recombinant protein expressed in E. coli. (scetibio.com)
- Thermodynamic characterization of the binding and cooperative interactions among gal-repressor, catabolite activator protein (CAP), and RNA polymerase as a function of the allosteric regulatory molecules galactose and cAMP is proposed in order to develop a comprehensive physical- chemical description of the regulation of the goal operon. (elsevier.com)
- These mutations appear to alter the structure and function of the POLR1D protein, which reduces the amount of functional RNA polymerase I and RNA polymerase III in cells. (medlineplus.gov)
Nucleic1
- Nucleic acid amplification (NAA) tests, such as polymerase chain reaction (PCR) and other methods for amplifying DNA and RNA, may facilitate rapid detection of microorganisms. (cdc.gov)
Transcription2
- We show that HelD prevents non-specific interactions between RNAP and DNA and dissociates stalled transcription elongation complexes. (nih.gov)
- Liu X, Bushnell DA, Kornberg RD. RNA polymerase II transcription: structure and mechanism. (harvard.edu)
Gene1
- The POLR1D gene provides instructions for making one part (subunit) of two related enzymes called RNA polymerase I and RNA polymerase III. (medlineplus.gov)
Enzymes1
- Enzymes that catalyze DNA template-directed extension of the 3'-end of an RNA strand one nucleotide at a time. (bvsalud.org)
Nucleotide2
- First, the polymerase backtracks to extrude the misincorporated nucleotide. (harvard.edu)
- DNA is composed of alternating sugar and phosphate groups, with the sugar attached to 1 of 4 possible nucleotide bases (adenosine, cytosine, guanine, thymidine). (cdc.gov)
Mycobacterial2
Abstract1
- ABSTRACT We evaluated the COBAS AMPLICOR polymerase chain reaction (PCR) based test for the detection of Mycobacterium tuberculosis complex in 866 respiratory and non-respiratory samples. (who.int)
Macromolecules2
Transcribe2
- RNA polymerases read the codes from specific areas of the DNA and transcribe the information into a mRNA copy of the DNA. (cdc.gov)
- This tumor type is associated with the biallelic loss of exons that transcribe a messenger RNA of 4,772 kb. (bvsalud.org)
Genes1
- The total chromosomal content of a cell involves approximately 105 genes in a specialized macromolecule of deoxyribonucleic acid (DNA). (cdc.gov)
Motif1
- DNA and RNA polymerases share a core architecture composed of three structurally conserved motifs: A, B, and C. Although the amino acid sequences of these motifs are highly conserved between closely related organisms, variation across broader evolutionary distances suggests that only a few residues in each motif are indispensable for polymerase function. (nebraska.edu)
Infection1
- HCV infection was confirmed by anti-HCV and HCV RNA in 1 of 7 HCWs with OBI. (who.int)
Sequence2
- P.6 left column 3rd paragraph:'The trigger loop is a conserved feature of all multisubunit, DNA-directed RNA polymerases, either observed in structures, such as that of the T. thermophilus RNAP [ref 71], or indicated by sequence analysis, as for E. coli and archaeal (M. jannaschii) RNAPs [refs 72,73]. (harvard.edu)
- 1. Is electrophilic or can be metabolical y activated to electrophiles does not alter the linear sequence of nucleotides (or bases) in the DNA, 2. (who.int)
Hepatitis3
- lope, bovine herpes virus glycoprotein, and Hence, DNA vaccine vectors have been de- hepatitis B surface antigen (2,4-8). (who.int)
- We tested 132 HCWs for hepatitis B virus (HBV) DNA by nested polymerase chain reaction (PCR), and hepatitis C virus antibody (anti-HCV) by ELISA. (who.int)
- This problem is ag- HCWs were recruited on the basis of Seven serum samples that were positive gravated by low hepatitis B vaccination accepting study enrolment without coverage, which was only 14% among for HBV DNA by nested PCR under- any random selection. (who.int)
20201
- METHODOLOGY: A cross-sectional study was conducted in the City of Maputo from 19 to 28 October 2020 through direct observation of mask use of all individuals present in markets, supermarkets and bus terminals. (cdc.gov)
Chain2
- RNA polymerase, beta subunit, conserved site / RNA polymerase Rpb2, domain 7 / RNA polymerase Rpb2, domain 3 / RNA polymerase Rpb2, OB-fold / RNA polymerase Rpb2, domain 7 / RNA polymerase Rpb2, domain 3 / RNA polymerases beta chain signature. (pdbj.org)
- All samples sis , the polymerase chain reaction (PCR) is were unique, each sample represented 1 the most widely used, best studied and patient, and duplicate samples were exclud- most widely published amplification tech- ed from this study. (who.int)
Type1
- In eukaryotes, three forms of the enzyme have been distinguished on the basis of sensitivity to alpha-amanitin, and the type of RNA synthesized. (bvsalud.org)
Humans1
- DNA vaccines in humans and the very limited information that is available from early clinical studies. (who.int)
Expression2
- The combi- onstrated in mice, induced by particle bom- nation of the essential elements yields a eu- bardment with gold beads coated with DNA karyotic expression vector that is capable of encoding human growth hormone and hu- driving the production of the antigen of in- man a-1 antitrypsin (3). (who.int)
- DNA vaccines were used to immunize ani- expression. (who.int)
Mechanism2
- The proposed studies will focus on determining the mechanism of the cooperative interactions among the three binding sites and determining if the contacts between the repressor and DNA affect the cooperative interactions. (elsevier.com)
- Studies are proposed to determine if gal-repressor binds cooperatively to DNA and if so, to determine the mechanism. (elsevier.com)
Structure1
- Other issues to be considered include determining how the geometric relationship of the repressor binding affects interaction between sites, and if local changes in DNA structure play a role in mediating cooperativity. (elsevier.com)
Complex1
- An NAA test for Mycobacterium tuberculosis complex (Amplified Mycobacterium Tuberculosis Direct Test or MTD {Gen-Probe{Registered}, San Diego, California}) * was recently approved by the Food and Drug Administration (FDA) for use on processed clinical specimens (1), and others are under development. (cdc.gov)
Alterations2
Agriculture1
- Sweetpotato whitefly, Bemisia tabaci MED/Q and MEAM1/B, are two economically important invasive species that cause considerable damages to agriculture crops through direct feeding and indirect vectoring of plant pathogens. (biomedcentral.com)
Indirect2
Types1
- Symposium "The Third Revolution summarizes the types of DNA vaccine vectors in common use, the on Vaccines: DNA Vaccines", immune responses and protective responses that have been obtained in Belo Horizonte, MG, Brasil, animal models, the safety considerations pertinent to the evaluation of November 3-7, 1997. (who.int)
Specific1
- In contrast, gal-repressor binds to two specific-sites separated by many turns of the DNA-helix. (elsevier.com)
Complete1
- Direct macromolecule damage by radiation involves partial or complete energy transfer to one or more electrons on the molecule. (cdc.gov)
Control1
- Thus, carcinogens nogenic are polycyclic aromatic hy- to induce DNA damage, it can be may act not only by producing DNA drocarbons and benzene, which by cal ed a genotoxicant or a genotox- damage directly but also by altering themselves are relatively inert chem- in, and if it is shown that the agent the processes that control normal ical y. (who.int)
Laboratory1
- ry and non-respiratory samples received at Direct microscopy, culture on Lowen- our TB laboratory. (who.int)
Directly1
- Further development of the footprint titration method is proposed in order to directly measure repressor binding to supercoiled DNA. (elsevier.com)
Virus2
- Nous avons examiné 132 agents de santé à la recherche d'ADN du virus de l'hépatite B (VHB) au moyen de l'amplification en chaîne par polymérase (PCR) nichée et de l'anticorps du virus de l'hépatite C (anti-VHC) par la méthode ELISA. (who.int)
- Influenza is a single-stranded, helically shaped, RNA virus of the orthomyxovirus family. (cdc.gov)
Process1
- ture of the mistake, the flanking se- in a process termed metabolic acti- quence, the presence of DNA dam- vation ( Mil er, 1970 ). (who.int)
Term1
- Examples of direct-acting elec- all have an impact on the outcome trophilic carcinogens are formalde- The term "genotoxic" refers to an of this proces s (Arana and Kunkel, hyde, sulfur mustard, and ethylene agent that induces DNA damage, 2010) . (who.int)