Motifs in DNA- and RNA-binding proteins whose amino acids are folded into a single structural unit around a zinc atom. In the classic zinc finger, one zinc atom is bound to two cysteines and two histidines. In between the cysteines and histidines are 12 residues which form a DNA binding fingertip. By variations in the composition of the sequences in the fingertip and the number and spacing of tandem repeats of the motif, zinc fingers can form a large number of different sequence specific binding sites.
Four or five slender jointed digits in humans and primates, attached to each HAND.
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.
Proteins which bind to DNA. The family includes proteins which bind to both double- and single-stranded DNA and also includes specific DNA binding proteins in serum which can be used as markers for malignant diseases.
Endogenous substances, usually proteins, which are effective in the initiation, stimulation, or termination of the genetic transcription process.
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.
Inorganic compounds that contain zinc as an integral part of the molecule.
A compound given in the treatment of conditions associated with zinc deficiency such as acrodermatitis enteropathica. Externally, zinc sulfate is used as an astringent in lotions and eye drops. (Reynolds JEF(Ed): Martindale: The Extra Pharmacopoeia (electronic version). Micromedex, Inc, Englewood, CO, 1995)
A family of zinc finger transcription factors that share homology with Kruppel protein, Drosophila. They contain a highly conserved seven amino acid spacer sequence in between their ZINC FINGER MOTIFS.
The sequence of PURINES and PYRIMIDINES in nucleic acids and polynucleotides. It is also called nucleotide sequence.
A mild astringent and topical protectant with some antiseptic action. It is also used in bandages, pastes, ointments, dental cements, and as a sunblock.
Proteins which maintain the transcriptional quiescence of specific GENES or OPERONS. Classical repressor proteins are DNA-binding proteins that are normally bound to the OPERATOR REGION of an operon, or the ENHANCER SEQUENCES of a gene until a signal occurs that causes their release.
The parts of a macromolecule that directly participate in its specific combination with another molecule.
The degree of similarity between sequences of amino acids. This information is useful for the analyzing genetic relatedness of proteins and species.
Stable zinc atoms that have the same atomic number as the element zinc, but differ in atomic weight. Zn-66-68, and 70 are stable zinc isotopes.
The process in which substances, either endogenous or exogenous, bind to proteins, peptides, enzymes, protein precursors, or allied compounds. Specific protein-binding measures are often used as assays in diagnostic assessments.
One of several general transcription factors that are specific for RNA POLYMERASE III. It is a zinc finger (ZINC FINGERS) protein and is required for transcription of 5S ribosomal genes.
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).
The level of protein structure in which combinations of secondary protein structures (alpha helices, beta sheets, loop regions, and motifs) pack together to form folded shapes called domains. Disulfide bridges between cysteines in two different parts of the polypeptide chain along with other interactions between the chains play a role in the formation and stabilization of tertiary structure. Small proteins usually consist of only one domain but larger proteins may contain a number of domains connected by segments of polypeptide chain which lack regular secondary structure.
A salt produced by the reaction of zinc oxide with acetic acid and used as an astringent, styptic, and emetic.
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.
A zinc-binding domain defined by the sequence Cysteine-X2-Cysteine-X(9-39)-Cysteine-X(l-3)-His-X(2-3)-Cysteine-X2-Cysteine -X(4-48)-Cysteine-X2-Cysteine, where X is any amino acid. The RING finger motif binds two atoms of zinc, with each zinc atom ligated tetrahedrally by either four cysteines or three cysteines and a histidine. The motif also forms into a unitary structure with a central cross-brace region and is found in many proteins that are involved in protein-protein interactions. The acronym RING stands for Really Interesting New Gene.
Proteins that have one or more tightly bound metal ions forming part of their structure. (Dorland, 28th ed)
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 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.
Proteins found in the nucleus of a cell. Do not confuse with NUCLEOPROTEINS which are proteins conjugated with nucleic acids, that are not necessarily present in the nucleus.
A metallic element of atomic number 30 and atomic weight 65.38. It is a necessary trace element in the diet, forming an essential part of many enzymes, and playing an important role in protein synthesis and in cell division. Zinc deficiency is associated with ANEMIA, short stature, HYPOGONADISM, impaired WOUND HEALING, and geophagia. It is known by the symbol Zn.
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.
Recombinant proteins produced by the GENETIC TRANSLATION of fused genes formed by the combination of NUCLEIC ACID REGULATORY SEQUENCES of one or more genes with the protein coding sequences of one or more genes.
Bones that make up the SKELETON of the FINGERS, consisting of two for the THUMB, and three for each of the other fingers.
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.
Established cell cultures that have the potential to propagate indefinitely.
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 biosynthesis of RNA carried out on a template of DNA. The biosynthesis of DNA from an RNA template is called REVERSE TRANSCRIPTION.
A painful disability in the hand affecting the finger or thumb. It is caused by mechanical impingement of the digital flexor tendons as they pass through a narrowed retinacular pulley at the level of the metacarpal head. Thickening of the sheath and fibrocartilaginous metaplasia can occur, and nodules can form. (From Green's Operative Hand Surgery, 5th ed, p2137-58).
An early growth response transcription factor that has been implicated in regulation of CELL PROLIFERATION and APOPTOSIS.
Any of the processes by which nuclear, cytoplasmic, or intercellular factors influence the differential control (induction or repression) of gene action at the level of transcription or translation.
Transport proteins that carry specific substances in the blood or across cell membranes.
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.
Screening techniques first developed in yeast to identify genes encoding interacting proteins. Variations are used to evaluate interplay between proteins and other molecules. Two-hybrid techniques refer to analysis for protein-protein interactions, one-hybrid for DNA-protein interactions, three-hybrid interactions for RNA-protein interactions or ligand-based interactions. Reverse n-hybrid techniques refer to analysis for mutations or other small molecules that dissociate known interactions.
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.
A ZINC FINGER MOTIF containing transcription factor that was originally identified as one of the IMMEDIATE-EARLY PROTEINS. It shuttles between the CYTOPLASM and the CELL NUCLEUS and is involved in destabilization of mRNAs for TUMOR NECROSIS FACTOR-ALPHA.
Procedures by which protein structure and function are changed or created in vitro by altering existing or synthesizing new structural genes that direct the synthesis of proteins with sought-after properties. Such procedures may include the design of MOLECULAR MODELS of proteins using COMPUTER GRAPHICS or other molecular modeling techniques; site-specific mutagenesis (MUTAGENESIS, SITE-SPECIFIC) of existing genes; and DIRECTED MOLECULAR EVOLUTION techniques to create new genes.
Constituent of the 50S subunit of prokaryotic ribosomes containing about 120 nucleotides and 34 proteins. It is also a constituent of the 60S subunit of eukaryotic ribosomes. 5S rRNA is involved in initiation of polypeptide synthesis.
Any of the processes by which nuclear, cytoplasmic, or intercellular factors influence the differential control of gene action during the developmental stages of an organism.
Processes that stimulate the GENETIC TRANSCRIPTION of a gene or set of genes.
A low-molecular-weight (approx. 10 kD) protein occurring in the cytoplasm of kidney cortex and liver. It is rich in cysteinyl residues and contains no aromatic amino acids. Metallothionein shows high affinity for bivalent heavy metals.
Diffusible gene products that act on homologous or heterologous molecules of viral or cellular DNA to regulate the expression of proteins.
The uptake of naked or purified DNA by CELLS, usually meaning the process as it occurs in eukaryotic cells. It is analogous to bacterial transformation (TRANSFORMATION, BACTERIAL) and both are routinely employed in GENE TRANSFER TECHNIQUES.
A transcription factor that plays a role as a key regulator of HEMATOPOIESIS. Aberrant Ikaros expression has been associated with LYMPHOBLASTIC LEUKEMIA.
Isoforms encoded by the WT1 Wilms tumor suppressor gene (GENES, WILMS TUMOR) and produced by alternative splicings. They are zinc finger-containing transcription factors involved in both transactivation and repression, and are critical for normal development and function of the urogenital tract.
Models used experimentally or theoretically to study molecular shape, electronic properties, or interactions; includes analogous molecules, computer-generated graphics, and mechanical structures.
Genetically engineered MUTAGENESIS at a specific site in the DNA molecule that introduces a base substitution, or an insertion or deletion.
Proteins that originate from insect species belonging to the genus DROSOPHILA. The proteins from the most intensely studied species of Drosophila, DROSOPHILA MELANOGASTER, are the subject of much interest in the area of MORPHOGENESIS and development.
Within a eukaryotic cell, a membrane-limited body which contains chromosomes and one or more nucleoli (CELL NUCLEOLUS). The nuclear membrane consists of a double unit-type membrane which is perforated by a number of pores; the outermost membrane is continuous with the ENDOPLASMIC RETICULUM. A cell may contain more than one nucleus. (From Singleton & Sainsbury, Dictionary of Microbiology and Molecular Biology, 2d ed)
Commonly observed structural components of proteins formed by simple combinations of adjacent secondary structures. A commonly observed structure may be composed of a CONSERVED SEQUENCE which can be represented by a CONSENSUS SEQUENCE.
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.
Proteins prepared by recombinant DNA technology.
A group of transcription factors that were originally described as being specific to ERYTHROID CELLS.
A thiol-containing non-essential amino acid that is oxidized to form CYSTINE.
CELL LINES derived from the CV-1 cell line by transformation with a replication origin defective mutant of SV40 VIRUS, which codes for wild type large T antigen (ANTIGENS, POLYOMAVIRUS TRANSFORMING). They are used for transfection and cloning. (The CV-1 cell line was derived from the kidney of an adult male African green monkey (CERCOPITHECUS AETHIOPS).)
Proteins encoded by homeobox genes (GENES, HOMEOBOX) that exhibit structural similarity to certain prokaryotic and eukaryotic DNA-binding proteins. Homeodomain proteins are involved in the control of gene expression during morphogenesis and development (GENE EXPRESSION REGULATION, DEVELOPMENTAL).
The distal part of the arm beyond the wrist in humans and primates, that includes the palm, fingers, and thumb.
A GATA transcription factor that is expressed in the MYOCARDIUM of developing heart and has been implicated in the differentiation of CARDIAC MYOCYTES. GATA4 is activated by PHOSPHORYLATION and regulates transcription of cardiac-specific genes.
Extrachromosomal, usually CIRCULAR DNA molecules that are self-replicating and transferable from one organism to another. They are found in a variety of bacterial, archaeal, fungal, algal, and plant species. They are used in GENETIC ENGINEERING as CLONING VECTORS.
Proteins found in any species of fungus.
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.
Genes whose expression is easily detectable and therefore used to study promoter activity at many positions in a target genome. In recombinant DNA technology, these genes may be attached to a promoter region of interest.
The first continuously cultured human malignant CELL LINE, derived from the cervical carcinoma of Henrietta Lacks. These cells are used for VIRUS CULTIVATION and antitumor drug screening assays.
Proteins that bind to RNA molecules. Included here are RIBONUCLEOPROTEINS and other proteins whose function is to bind specifically to RNA.
Proteins obtained from various species of Xenopus. Included here are proteins from the African clawed frog (XENOPUS LAEVIS). Many of these proteins have been the subject of scientific investigations in the area of MORPHOGENESIS and development.
Proteins encoded by the GAG GENE of the HUMAN IMMUNODEFICIENCY VIRUS.
The act, process, or result of passing from one place or position to another. It differs from LOCOMOTION in that locomotion is restricted to the passing of the whole body from one place to another, while movement encompasses both locomotion but also a change of the position of the whole body or any of its parts. Movement may be used with reference to humans, vertebrate and invertebrate animals, and microorganisms. Differentiate also from MOTOR ACTIVITY, movement associated with behavior.
The characteristic 3-dimensional shape of a protein, including the secondary, supersecondary (motifs), tertiary (domains) and quaternary structure of the peptide chain. PROTEIN STRUCTURE, QUATERNARY describes the conformation assumed by multimeric proteins (aggregates of more than one polypeptide chain).
A genus of small, two-winged flies containing approximately 900 described species. These organisms are the most extensively studied of all genera from the standpoint of genetics and cytology.
A GATA transcription factor that is specifically expressed in hematopoietic lineages and plays an important role in the CELL DIFFERENTIATION of ERYTHROID CELLS and MEGAKARYOCYTES.
Genes at loci that are involved in the development of WILMS TUMOR. Included are human WT1 at 11p13 and human WT2 (MTACR1) at 11p15.
Promoter-specific RNA polymerase II transcription factor that binds to the GC box, one of the upstream promoter elements, in mammalian cells. The binding of Sp1 is necessary for the initiation of transcription in the promoters of a variety of cellular and viral GENES.
Proteins that are coded by immediate-early genes, in the absence of de novo protein synthesis. The term was originally used exclusively for viral regulatory proteins that were synthesized just after viral integration into the host cell. It is also used to describe cellular proteins which are synthesized immediately after the resting cell is stimulated by extracellular signals.
Proteins obtained from the species SACCHAROMYCES CEREVISIAE. The function of specific proteins from this organism are the subject of intense scientific interest and have been used to derive basic understanding of the functioning similar proteins in higher eukaryotes.
An early growth response transcription factor that controls the formation of the MYELIN SHEATH around peripheral AXONS by SCHWANN CELLS. Mutations in EGR2 transcription factor have been associated with HEREDITARY MOTOR AND SENSORY NEUROPATHIES such as CHARCOT-MARIE-TOOTH DISEASE.
The integration of exogenous DNA into the genome of an organism at sites where its expression can be suitably controlled. This integration occurs as a result of homologous recombination.
A continuing periodic change in displacement with respect to a fixed reference. (McGraw-Hill Dictionary of Scientific and Technical Terms, 6th ed)
The relationship between the chemical structure of a compound and its biological or pharmacological activity. Compounds are often classed together because they have structural characteristics in common including shape, size, stereochemical arrangement, and distribution of functional groups.
Force exerted when gripping or grasping.
Deletion of sequences of nucleic acids from the genetic material of an individual.
An electrophoretic technique for assaying the binding of one compound to another. Typically one compound is labeled to follow its mobility during electrophoresis. If the labeled compound is bound by the other compound, then the mobility of the labeled compound through the electrophoretic medium will be retarded.
A technique that localizes specific nucleic acid sequences within intact chromosomes, eukaryotic cells, or bacterial cells through the use of specific nucleic acid-labeled probes.
A diverse class of enzymes that interact with UBIQUITIN-CONJUGATING ENZYMES and ubiquitination-specific protein substrates. Each member of this enzyme group has its own distinct specificity for a substrate and ubiquitin-conjugating enzyme. Ubiquitin-protein ligases exist as both monomeric proteins multiprotein complexes.
A family of transcription factors that are induced by GROWTH FACTORS and contain a highly conserved DNA-binding domain composed of three ZINC FINGER MOTIFS.
Use of restriction endonucleases to analyze and generate a physical map of genomes, genes, or other segments of DNA.
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.
The first digit on the radial side of the hand which in humans lies opposite the other four.
The phenotypic manifestation of a gene or genes by the processes of GENETIC TRANSCRIPTION and GENETIC TRANSLATION.
Process of generating a genetic MUTATION. It may occur spontaneously or be induced by MUTAGENS.
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.
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)
An idiopathic vascular disorder characterized by bilateral Raynaud phenomenon, the abrupt onset of digital paleness or CYANOSIS in response to cold exposure or stress.
Progressive restriction of the developmental potential and increasing specialization of function that leads to the formation of specialized cells, tissues, and organs.

A Drosophila doublesex-related gene, terra, is involved in somitogenesis in vertebrates. (1/4650)

The Drosophila doublesex (dsx) gene encodes a transcription factor that mediates sex determination. We describe the characterization of a novel zebrafish zinc-finger gene, terra, which contains a DNA binding domain similar to that of the Drosophila dsx gene. However, unlike dsx, terra is transiently expressed in the presomitic mesoderm and newly formed somites. Expression of terra in presomitic mesoderm is restricted to cells that lack expression of MyoD. In vivo, terra expression is reduced by hedgehog but enhanced by BMP signals. Overexpression of terra induces rapid apoptosis both in vitro and in vivo, suggesting that a tight regulation of terra expression is required during embryogenesis. Terra has both human and mouse homologs and is specifically expressed in mouse somites. Taken together, our findings suggest that terra is a highly conserved protein that plays specific roles in early somitogenesis of vertebrates.  (+info)

ETO-2, a new member of the ETO-family of nuclear proteins. (2/4650)

The t(8;21) is associated with 12-15% of acute myelogenous leukemias of the M2 subtype. The translocation results in the fusion of two genes, AML1 (CBFA2) on chromosome 21 and ETO (MTG8) on chromosome 8. AML1 encodes a DNA binding factor; the ETO protein product is less well characterized, but is thought to be a transcription factor. Here we describe the isolation and characterization of ETO-2, a murine cDNA that encodes a new member of the ETO family of proteins. ETO-2 is 75% identical to murine ETO and shares very high sequence identities over four regions of the protein with ETO (domain I-III and zinc-finger). Northern analysis identifies ETO-2 transcripts in many of the murine tissues analysed and in the developing mouse embryo. ETO-2 is also expressed in myeloid and erythroid cell lines. We confirmed the nuclear localization of ETO-2 and demonstrated that domain III and the zinc-finger region are not required for nuclear localization. We further showed that a region within ETO, containing domain II, mediates dimerization among family members. This region is conserved in the oncoprotein AML-1/ETO. The recent identification of another ETO-like protein, myeloid translocation gene-related protein 1, together with the data presented here, demonstrates that at least three ETO proteins exist with the potential to form dimers in the cell nucleus.  (+info)

Nrg1 is a transcriptional repressor for glucose repression of STA1 gene expression in Saccharomyces cerevisiae. (3/4650)

Expression of genes encoding starch-degrading enzymes is regulated by glucose repression in the yeast Saccharomyces cerevisiae. We have identified a transcriptional repressor, Nrg1, in a genetic screen designed to reveal negative factors involved in the expression of STA1, which encodes a glucoamylase. The NRG1 gene encodes a 25-kDa C2H2 zinc finger protein which specifically binds to two regions in the upstream activation sequence of the STA1 gene, as judged by gel retardation and DNase I footprinting analyses. Disruption of the NRG1 gene causes a fivefold increase in the level of the STA1 transcript in the presence of glucose. The expression of NRG1 itself is inhibited in the absence of glucose. DNA-bound LexA-Nrg1 represses transcription of a target gene 10.7-fold in a glucose-dependent manner, and this repression is abolished in both ssn6 and tup1 mutants. Two-hybrid and glutathione S-transferase pull-down experiments show an interaction of Nrg1 with Ssn6 both in vivo and in vitro. These findings indicate that Nrg1 acts as a DNA-binding repressor and mediates glucose repression of the STA1 gene expression by recruiting the Ssn6-Tup1 complex.  (+info)

The mouse Aire gene: comparative genomic sequencing, gene organization, and expression. (4/4650)

Mutations in the human AIRE gene (hAIRE) result in the development of an autoimmune disease named APECED (autoimmune polyendocrinopathy candidiasis ectodermal dystrophy; OMIM 240300). Previously, we have cloned hAIRE and shown that it codes for a putative transcription-associated factor. Here we report the cloning and characterization of Aire, the murine ortholog of hAIRE. Comparative genomic sequencing revealed that the structure of the AIRE gene is highly conserved between human and mouse. The conceptual proteins share 73% homology and feature the same typical functional domains in both species. RT-PCR analysis detected three splice variant isoforms in various mouse tissues, and interestingly one isoform was conserved in human, suggesting potential biological relevance of this product. In situ hybridization on mouse and human histological sections showed that AIRE expression pattern was mainly restricted to a few cells in the thymus, calling for a tissue-specific function of the gene product.  (+info)

Identification and characterization of a zinc finger gene (ZNF213) from 16p13.3. (5/4650)

During our search for the familial Mediterranean fever (FMF) gene, we identified by cDNA selection a 1.2 kb cDNA fragment representing a novel human gene that is expressed in a wide variety of tissues. This gene spans approx. 8.0 kb genomic DNA and has seven exons. Its 3' untranslated region contains a long tandem repeat that gives rise to a polymorphism with two alleles of approx. 1.1 kb and 1.0 kb, with the 1.1 kb allele in strong linkage disequilibrium with FMF in patients of different ethnic backgrounds. However, both genetic and mutational analyses have excluded this gene as the one responsible for FMF. The predicted 424 amino acid protein, designated ZNF213, contains three C2H2 zinc fingers, a Kruppel associated A box and a leucine rich motif (LeR domain/SCAN box), strongly suggestive of a transcription factor.  (+info)

Leukemia translocation protein PLZF inhibits cell growth and expression of cyclin A. (6/4650)

The PLZF gene was identified by its fusion with the RARalpha locus in a therapy resistant form of acute promyelocytic leukemia (APL) associated with the t(11;17)(q23;q21) translocation. Here we describe PLZF as a negative regulator of cell cycle progression ultimately leading to growth suppression. PLZF can bind and repress the cyclin A2 promoter while expression of cyclin A2 reverts the growth suppressed phenotype of myeloid cells expressing PLZF. In contrast RARalpha-PLZF, a fusion protein generated in t(11;17)(q23;q21)-APL activates cyclin A2 transcription and allows expression of cyclin A in anchorage-deprived NIH3T3 cells. Therefore, cyclin A2 is a candidate target gene for PLZF and inhibition of cyclin A expression may contribute to the growth suppressive properties of PLZF. Deregulation of cyclin A2 by RARalpha-PLZF may represent an oncogenic mechanism of this chimeric protein and contribute to the aggressive clinical phenotype of t(11;17)(q23;q21)-associated APL.  (+info)

RFLAT-1: a new zinc finger transcription factor that activates RANTES gene expression in T lymphocytes. (7/4650)

RANTES (Regulated upon Activation, Normal T cell Expressed and Secreted) is a chemoattractant cytokine (chemokine) important in the generation of inflammatory infiltrate and human immunodeficiency virus entry into immune cells. RANTES is expressed late (3-5 days) after activation in T lymphocytes. Using expression cloning, we identified the first "late" T lymphocyte associated transcription factor and named it "RANTES Factor of Late Activated T Lymphocytes-1" (RFLAT-1). RFLAT-1 is a novel, phosphorylated, zinc finger transcription factor that is expressed in T cells 3 days after activation, coincident with RANTES expression. While Rel proteins play the dominant role in RANTES gene expression in fibroblasts, RFLAT-1 is a strong transactivator for RANTES in T cells.  (+info)

Mapping the functional domains of BRCA1. Interaction of the ring finger domains of BRCA1 and BARD1. (8/4650)

Breast cancer 1 (BRCA1) and BRCA1-associated RING domain 1 (BARD1) are multidomain proteins that interact in vivo via their N-terminal RING finger motif regions. To characterize functional aspects of the BRCA1/BARD1 interaction, we have defined the structural domains required for the interaction, as well as their oligomerization state, relative stability, and possible nucleic acid binding activity. We have found that the RING finger motifs do not themselves constitute stable structural domains but are instead part of larger domains comprising residues 1-109 of BRCA1 and residues 26-119 of BARD1. These domains exist as homodimers and preferentially form a stable heterodimer. Shorter BRCA1 RING finger constructs do not interact with BARD1 or with longer BRCA1 constructs, indicating that the heterodimeric and homodimer interactions are mediated by regions outside the canonical RING finger motif. Nucleic acid binding is a generally proposed function of RING finger domains. We show that neither the homodimers nor the heterodimer displays affinity for nucleic acids, indicating that the proposed roles of BRCA1 and BARD1 in DNA repair and/or transcriptional activation must be mediated either by other regions of the proteins or by additional cofactors.  (+info)

TY - JOUR. T1 - Custom DNA-binding proteins come of age. T2 - Polydactyl zinc-finger proteins. AU - Segal, David. AU - Barbas, Carlos F.. PY - 2001/12/1. Y1 - 2001/12/1. N2 - Artificial transcription factors based on modified zinc-finger DNA-binding domains have been shown to activate or repress the transcription of endogenous genes in multiple organisms. Advances in both the construction of novel zinc-finger proteins and our understanding of the characteristics of a productive regulatory site have fueled these achievements.. AB - Artificial transcription factors based on modified zinc-finger DNA-binding domains have been shown to activate or repress the transcription of endogenous genes in multiple organisms. Advances in both the construction of novel zinc-finger proteins and our understanding of the characteristics of a productive regulatory site have fueled these achievements.. UR - http://www.scopus.com/inward/record.url?scp=0035712253&partnerID=8YFLogxK. UR - ...
Zinc-finger nucleases (ZFNs) are artificial restriction enzymes generated by fusing a zinc finger DNA-binding domain to a DNA-cleavage domain. Zinc finger domains can be engineered to target specific desired DNA sequences and this enables zinc-finger nucleases to target unique sequences within complex genomes. By taking advantage of endogenous DNA repair machinery, these reagents can be used to precisely alter the genomes of higher organisms. Alongside CRISPR/Cas9 and TALEN, ZFN is a prominent tool in the field of genome editing. The DNA-binding domains of individual ZFNs typically contain between three and six individual zinc finger repeats and can each recognize between 9 and 18 basepairs. If the zinc finger domains perfectly recognize a 3 basepair DNA sequence to generate a 3-finger array that can recognize a 9 basepair target site. Other procedures can utilize either 1-finger or 2-finger modules to generate zinc-finger arrays with six or more individual zinc fingers. The main drawback with ...
Read Functions of the CCCH type zinc finger protein OsGZF1 in regulation of the seed storage protein GluB-1 from rice, Plant Molecular Biology on DeepDyve, the largest online rental service for scholarly research with thousands of academic publications available at your fingertips.
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A zinc finger motif is an element of proteins that can specifically recognize and bind to DNA. Because they contain multiple cysteine residues, zinc finger motifs possess redox properties. Ionizing radiation generates a variety of free radicals in organisms. Zinc finger motifs, therefore, may be a target of ionizing radiation. The effect of gamma radiation on the zinc finger motifs in transcription factor IIIA (TFIIIA), a zinc finger protein, was investigated. TFIIIA was exposed to different gamma doses from 60Co sources. The dose rates were 0.20 Gy/min and 800 Gy/h, respectively. The binding capacity of zinc finger motifs in TFIIIA was determined using an electrophoretic mobility shift assay. We found that 1000 Gy of gamma radiation impaired the function of the zinc finger... motifs in TFIIIA. The sites of radiation-induced damage in the zinc finger were the thiol groups of cysteine residues and zinc (II) ions. The thiol groups were oxidized to form disulfide bonds and the zinc (II) ions were ...
We have taken a comprehensive approach to the generation of novel DNA binding zinc finger domains of defined specificity. Herein we describe the generation and characterization of a family of zinc finger domains developed for the recognition of each of the 16 possible 3-bp DNA binding sites having the sequence 5-GNN-3. Phage display libraries of zinc finger proteins were created and selected under conditions that favor enrichment of sequence-specific proteins. Zinc finger domains recognizing a number of sequences required refinement by site-directed mutagenesis that was guided by both phage selection data and structural information. In many cases, residues not expected to make base-specific contacts had effects on specificity. A number of these domains demonstrate exquisite specificity and discriminate between sequences that differ by a single base with >100-fold loss in affinity. We conclude that the three helical positions -1, 3, and 6 of a zinc finger domain are insufficient to allow for ...
TY - JOUR. T1 - Differentiation dependent expression in muscle cells of ZT3, a novel zinc finger factor differentially expressed in embryonic and adult tissues. AU - Polimeni, M.. AU - Giorgi, S.. AU - De Gregorio, L.. AU - Dragani, T. A.. AU - Molinaro, M.. AU - Cossu, G.. AU - Bouché, M.. PY - 1996/1. Y1 - 1996/1. N2 - ZT3, isolated from a murine muscle cell cDNA library by a low-stringency hybridization, encodes a zinc finger domain containing factor with a transcript of 5.0 kb. A 3 2.5 kb partial nucleotide sequence contains an ORF of 1.5 kb where 17 canonical C2H2 zinc finger domains organized in tandem were identified. It maps on mouse chromosome 11, close to two mutations which affect skeletal formation. ZT3 expression depends upon differentiation of myogenic cells in culture, since it is upregulated with myogenin and inhibited in scr-transfected C2C12 cells. ZT3 is not expressed in NIH3T3 or C3H10T1/2 fibroblasts, but is induced when fibroblasts are myogenically converted by ...
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The corpus luteum (CL) is a temporary organ involved in the maintenance of pregnancy. In the course of its life-cycle, the CL undergoes two distinct and consecutive processes for its inevitable removal through apoptosis: functional and structural luteolysis. We isolated a gene encoding for a novel rat zinc finger protein (ZFP), named rat ZFP96 (rZFP96) from an ovarian lambda cDNA library. Sequence analysis revealed close sequence and structural similarity to mouse ZFP96 and human zinc finger protein 305 (ZNF305). Quantitative reverse transcription-polymerase chain reaction analysis revealed a positive correlation with the end of pregnancy, that is, the onset of structural luteolysis of the CL. Messenger RNA levels increased 3-fold (P < 0.01) between days 13 and 22 of pregnancy and 8-fold (P < 0.01) between day 13 of pregnancy and day 1 post-partum. In addition, we detected rZFP96 expression in mammary, placenta, heart, kidney and skeletal muscle. Sequence analysis predicted that rZFP96 has a ...
Zinc finger nucleases (ZFNs) are proteins composed of a DNA binding-domain and a DNA cleaving-domain. One zinc finger binding domain recognizes and binds to a three nucleotide sequence, one can thus increase the binding specificity of a ZFN by adding more zinc fingers. The DNA cleaving-domain (Fok 1 nuclease) can then be used to create a double-stranded break in DNA at the desired point (Fig. 1). After a double stranded break, DNA is repaired by non-homologous end joining. This often causes small insertions or deletions in the DNA, resulting frame-shift mutations. These frame-shifts result in nonsense mutations or nonsense-mediated decay. These effects are therefore very useful for creating knockout genes. Additionally, genetic material such as DNA plasmids can be integrated into a gene after a double stranded break. A desired donor plasmid will contain arms of DNA which are homologous to the ZFN cut site. The donor plasmid and ZFNs can then be added simultaneously to the cell, the genetic ...
Zinc finger proteins contain DNA-binding domains and have a wide variety of functions, most of which encompass some form of transcriptional activation or repression. The majority of zinc finger proteins contain a Krueppel-type DNA binding domain and a KRAB domain, which is thought to interact with KAP1, thereby recruiting histone modifying proteins. Zinc finger protein 75 (ZNF75), also known as ZNF82, is a 289 amino acid member of the Krueppel C2H2-type zinc finger protein family. Localized to the nucleus, ZNF75 contains five C2H2- type zinc fingers and one KRAB domain through which it is thought to be involved in DNA-binding and transcriptional regulation ...
Zinc finger inhibitors, or zinc ejectors, are substances or compounds that interact adversely with zinc fingers and cause them to release their zinc from its binding site, disrupting the conformation of the polypeptide chain and rendering the zinc fingers ineffective, thereby preventing them from performing their associated cellular functions. This is typically accomplished through chelation of the zinc binding site. As zinc fingers are known to be involved in m-RNA regulation, reverse transcription, protection of synthesized viral DNA, transcription inhibition, and initial integration processes, prevention of zinc finger function can have drastic effects on the function of the cell or virus. Zinc finger inhibitors are typically used to combat HIV. HIV treatments usually rely on targeting reverse transcriptases and proteases. However, these methods are proving to be ineffective due to the development of resistant strains of the virus or due to the stoppage of the treatment. This method of using ...
Artificial transcription factors based on modified zinc-finger DNA-binding domains have been shown to activate or repress the transcription of endogenous genes in multiple organisms. Advances in both the construction of novel zinc-finger proteins and our understanding of the characteristics of a productive regulatory site have fueled these achievements ...
Zinc finger nucleases (ZFNs) are associated with cell death and apoptosis by binding at countless undesired locations. This cytotoxicity is associated with the binding ability of engineered zinc finger domains to bind dissimilar DNA sequences with high affinity. In general, binding preferences of transcription factors are associated with significant degenerated diversity and complexity which convolutes the design and engineering of precise DNA binding domains. Evolutionary success of natural zinc finger proteins, however, evinces that nature created specific evolutionary traits and strategies, such as modularity and rank-specific recognition to cope with binding complexity that are critical for creating clinical viable tools to precisely modify the human genome. Our findings indicate preservation of general modularity and significant alteration of the rank-specific binding preferences of the three-finger binding domain of transcription factor SP1 when exchanging amino acids in the 2nd finger. ...
BACKGROUND ZNF32 has been predicted to be a zinc finger protein and is involved in cell differentiation and tumor development, but its precise function is unknown. Specific monoclonal antibodies (mAbs) have been widely used in research and clinical diagnosis and treatments. Therefore, we established an anti-ZNF32 mAb to characterize this proteins function. MATERIAL/METHODS Peptide⁴⁹⁻⁶³, a specific small peptide of ZNF32, was chosen and the synthetic keyhole limpet hemocyanin (KLH)-peptide⁴⁹⁻⁶³ was used as an antigen to immunize mice. A mAb against peptide⁴⁹⁻⁶³ was generated by hybridoma technology, and hybridoma cells were screened by limiting dilution. The isoform of mAb-pZNF32-8D9 was identified by double agar diffusion. The sensitivity and specificity of the mAb and expressed levels of ZNF32 in various cells and tissues were identified by enzyme-linked immunosorbent assay (ELISA), immunocytochemistry, immunohistochemistry, and Western blotting. RESULTS A stable anti
Plasmids for genome engineering using zinc finger nucleases (ZFN) constructed via modular assembly of artificial zinc finger arrays.
We report here an efficient method for targeted mutagenesis of Arabidopsis genes through regulated expression of zinc finger nucleases (ZFNs)-enzymes engineered to create DNA double-strand breaks at specific target loci. ZFNs recognizing the Arabidopsis ADH1 and TT4 genes were made by Oligomerized Pool ENgineering (OPEN)-a publicly available, selection-based platform that yields high quality zinc finger arrays. The ADH1 and TT4 ZFNs were placed under control of an estrogen-inducible promoter and introduced into Arabidopsis plants by floral-dip transformation. Primary transgenic Arabidopsis seedlings induced to express the ADH1 or TT4 ZFNs exhibited somatic mutation frequencies of 7% or 16%, respectively. The induced mutations were typically insertions or deletions (1-142 bp) that were localized at the ZFN cleavage site and likely derived from imprecise repair of chromosome breaks by nonhomologous end-joining. Mutations were transmitted to the next generation for 69% of primary transgenics expressing the
The maize INDETERMINATE1 gene, ID1, is a key regulator of the transition to flowering and the founding member of a transcription factor gene family that encodes a protein with a distinct arrangement of zinc finger motifs. The zinc fingers and surrounding sequence make up the signature ID domain (IDD), which appears to be found in all higher plant genomes. The presence of zinc finger domains and previous biochemical studies showing that ID1 binds to DNA suggests that members of this gene family are involved in transcriptional regulation. Comparison of IDD genes identified in Arabidopsis and rice genomes, and all IDD genes discovered in maize EST and genomic databases, suggest that ID1 is a unique member of this gene family. High levels of sequence similarity amongst all IDD genes from maize, rice and Arabidopsis suggest that they are derived from a common ancestor. Several unique features of ID1 suggest that it is a divergent member of the maize IDD family. Although no clear ID1 ortholog was identified
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1HVO: ZINC-AND SEQUENCE-DEPENDENT BINDING TO NUCLEIC ACIDS BY THE N-TERMINAL ZINC FINGER DOMAIN OF THE HIV-1 NUCLEOCAPSID PROTEIN: NMR STRUCTURE OF THE COMPLEX WITH THE PSI-SITE ANALOG, D/ACGCC
Zinc finger proteins (ZNFs) bind DNA and, through this binding, regulate gene transcription. Most ZNFs contain conserved C2H2 motifs and are classified as Kruppel-type zinc fingers. For a general description of these proteins, see ZNF91 (MIM 603971).[supplied by OMIM, Jul 2002]
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Blimp1, a zinc-finger containing DNA-binding transcriptional repressor, functions as a master regulator of B cell terminal differentiation. Considerable evidence suggests that Blimp1 is required for the establishment of anteroposterior axis formation and the formation of head structures during early vertebrate development. In mouse embryos, Blimp1 is strongly expressed in axial mesendoderm, the tissue known to provide anterior patterning signals during gastrulation. Here, we describe for the first time the defects caused by loss of Blimp1 function in the mouse. Blimp1 deficient embryos die at mid-gestation, but surprisingly early axis formation, anterior patterning and neural crest formation proceed normally. Rather, loss of Blimp1 expression disrupts morphogenesis of the caudal branchial arches and leads to a failure to correctly elaborate the labyrinthine layer of the placenta. Blimp1 mutant embryos also show widespread blood leakage and tissue apoptosis, and, strikingly, Blimp1 homozygous mutants
TY - JOUR. T1 - An internal deletion within an 11p13 zinc finger gene contributes to the development of Wilms tumor. AU - Haber, Daniel A.. AU - Buckler, Alan J.. AU - Glaser, Thomas M. AU - Call, Katherine M.. AU - Pelletier, Jerry. AU - Sohn, Robert L.. AU - Douglass, Edwin C.. AU - Housman, David E.. PY - 1990/6/29. Y1 - 1990/6/29. N2 - We have recently described the isolation of a candidate for the Wilms tumor susceptibility gene mapping to band p13 of human chromosome 11. This gene, primarily expressed in fetal kidney, appears to encode a DNA binding protein. We now describe a sporadic, unilateral Wilms tumor in which one allele of this gene contains a 25 bp deletion spanning an exon-intron junction and leading to aberrant mRNA splicing and loss of one of the four zinc finger consensus domains in the protein. The mutation is absent in the affected individuals germline, consistent with the somatic inactivation of a tumor suppressor gene. In addition to this intragenic deletion affecting ...
We have previously reported (Villa et al. (1993), Genomics 18: 223) the characterization of the human ZNF75 gene located on Xq26, which has only limited homology (less than 65%) to other ZF genes in the databases. Here, we describe three human zinc finger genes with 86 to 95% homology to ZNF75 at the nucleotide level, which represent all the members of the human ZNF75 subfamily. One of these, ZNF75B, is a pseudogene mapped to chromosome 12q13. The other two, ZNF75A and ZNF75C, maintain an ORF in the sequenced region, and at least the latter is expressed in the U937 cell line. They were mapped to chromosomes 16 and 11, respectively. All these genes are conserved in chimpanzees, gorillas, and orangutans. The ZNF75B homologue is a pseudogene in all three great apes, and in chimpanzee it is located on chromosome 10 (phylogenetic XII), at p13 (corresponding to the human 12q13). The chimpanzee homologue of ZNF75 is also located on the Xq26 chromosome, in the same region, as detected by in situ ...
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An inducible program of inflammatory gene expression is a hallmark of antimicrobial defenses. This response is controlled by a collaboration involving signal-dependent activation of transcription factors, transcriptional co-regulators, and chromatin-modifying factors. Here we have identified a highly conserved Zinc finger DNA binding protein CNBP (also called ZNF9) upregulated in myeloid cells exposed to lipopolysaccharide. CNBP resides primarily in the cytosol and upon TLR4 engagement, CNBP translocate to the nucleus. To investigate the functional consequences of these events, we generated mice lacking CNBP and characterized the role of CNBP in controlling the inducible transcriptional program using a combination of RNA-sequencing and multiplex gene expression analysis (Nanostring). In response to an array of signals such as LPS, CNBP-deficient macrophages were impaired in their ability to induce important immune genes including IL12p40 and IL6 amongst others. CNBP-deficient cells showed normal ...
EntrezGene ,Full_name_from_nomenclature_authority=CCCTC-binding factor (zinc finger protein) ,GeneID=10664 ,LocusTag=- ,Modification_date=20120108 ,Nomenclature_status=O ,Other_designations=11 zinc finger transcriptional repressor;;11-zinc finger protein;;CTCFL paralog;;transcriptional repressor CTCF ,Symbol=CTCF ,Symbol_from_nomenclature_authority=CTCF ,Synonyms=- ,chromosome=16 ,dbXrefs=HGNC:13723;;MIM:604167;;Ensembl:ENSG00000102974;;HPRD:05005;;Vega:OTTHUMG00000137539;;EpiFactors:10664:genes ,description=CCCTC-binding factor (zinc finger protein) ,map_location=16q21-q22.3 ,tax_id=9606 ,tf?=yes ,transcription_factor= ,type_of_gene=protein-coding ...
...RICHMOND Calif. Dec. 7 2010 /- Sangamo BioSciences In... Abst.# 647 Manipulating Higher Order Chromatin Structure of the Be...These data demonstrate the use of zinc finger DNA-binding proteins (ZF... Abst.# 3764 Editing Human Lymphocyte Specificity for Safe and Effe...,Sangamo,BioSciences,Announces,Data,Presentation,of,First,In,Vivo,Demonstration,of,ZFN-mediated,Gene,Correction,Via,Systemic,Delivery,at,American,Society,for,Hematology,Meeting,biological,advanced biology technology,biology laboratory technology,biology device technology,latest biology technology
Neale, Matt (2010) PRDM9 points the zinc finger at meiotic recombination hotspots. Genome Biology, 11 (2). p. 104. ISSN 14656914 Full text not available from this repository ...
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The H3K9me3 histone modification is often found at promoter regions, where it functions to repress transcription. However, we have previously shown that 3′ exons of zinc finger genes (ZNFs) are marked by high levels of H3K9me3. We have now further investigated this unusual location for H3K9me3 in ZNF genes. Neither bioinformatic nor experimental approaches support the hypothesis that the 3′ exons of ZNFs are promoters. We further characterized the histone modifications at the 3′ ZNF exons and found that these regions also contain H3K36me3, a mark of transcriptional elongation. A genome-wide analysis of ChIP-seq data revealed that ZNFs constitute the majority of genes that have high levels of both H3K9me3 and H3K36me3. These results suggested the possibility that the ZNF genes may be imprinted, with one allele transcribed and one allele repressed. To test the hypothesis that the contradictory modifications are due to imprinting, we used a SNP analysis of RNA-seq data to demonstrate that both
Zinc finger CCHC domain-containing protein 8 contains a PF00098 domain.. Zinc finger CCHC domain-containing protein 8 contains a PF04046 domain.. Zinc finger CCHC domain-containing protein 8 is proteolytically cut by granzyme B, human-type (S01.010) cleavage. MDED-ALTL.. ...
TY - JOUR. T1 - Egr3/Pilot, a zinc finger transcription factor, is rapidly regulated by activity in brain neurons and colocalizes with Egr1/zif268. AU - Yamagata, K.. AU - Kaufmann, W. E.. AU - Lanahan, A.. AU - Papapavlou, M.. AU - Barnes, Carol A. AU - Andreasson, K. I.. AU - Worley, P. F.. PY - 1994/7. Y1 - 1994/7. UR - http://www.scopus.com/inward/record.url?scp=0028466211&partnerID=8YFLogxK. UR - http://www.scopus.com/inward/citedby.url?scp=0028466211&partnerID=8YFLogxK. M3 - Article. C2 - 10467592. AN - SCOPUS:0028466211. VL - 1. SP - 140. EP - 152. JO - Learning and Memory. JF - Learning and Memory. SN - 1072-0502. IS - 2. ER - ...
TY - JOUR. T1 - Zinc finger protein 131 inhibits estrogen signaling by suppressing estrogen receptor α homo-dimerization. AU - Oh, Yohan. AU - Chung, Kwang Chul. PY - 2013/1/4. Y1 - 2013/1/4. N2 - Steroid hormone estrogen elicits various physiological functions, many of which are mediated through two structurally and functionally distinct estrogen receptors, ERα and ERβ. The functional role of zinc finger protein 131 (ZNF131) is poorly understood, but it is assumed to possess transcriptional regulation activity due to the presence of a DNA binding motif. A few recent reports, including ours, revealed that ZNF131 acts as a negative regulator of ERα and that SUMO modification potentiates the negative effect of ZNF131 on estrogen signaling. However, its molecular mechanism for ERα inhibition has not been elucidated in detail. Here, we demonstrate that ZNF131 directly interacts with ERα, which consequently inhibits ERα-mediated trans-activation by suppressing its homo-dimerization. Moreover, ...
TY - JOUR. T1 - Testicular zinc finger protein recruits histone deacetylase 2 and suppresses the transactivation function and intranuclear foci formation of agonist-bound androgen receptor competitively with TIF2. AU - Tao, Rong Hua. AU - Kawate, Hisaya. AU - Wu, Yin. AU - Ohnaka, Keizo. AU - Ishizuka, Masamichi. AU - Inoue, Atsuto. AU - Hagiwara, Hiromi. AU - Takayanagi, Ryoichi. PY - 2006/3/9. Y1 - 2006/3/9. N2 - We previously reported that testicular zinc finger protein (TZF) is a corepressor for androgen receptor (AR). The present study demonstrated that a central portion (amino acids 512-663) of TZF, TZF(512-663), is responsible for both binding to AR and repressing the transactivation. TZF recruited endogenous histone deacetylase 2 (HDAC2) and formed a complex with agonist-bound AR. Imaging analyses showed that TZF and TZF(512-663) were recruited by AR and simultaneously impaired distinct AR foci formation. Quantification of the foci number using a three-dimensional imaging method revealed ...
TY - JOUR. T1 - Zinc finger protein 28 as a novel melanoma-related molecule. AU - Yajima, Ichiro. AU - Kumasaka, Mayuko. AU - Thang, Nguyen Dinh. AU - Yanagishita, Takeshi. AU - Ohgami, Nobutaka. AU - Kallenberg, David. AU - Naito, Yuji. AU - Yoshikawa, Toshikazu. AU - Sakashita, Naomi. AU - Kato, Masashi. PY - 2009/7/1. Y1 - 2009/7/1. KW - Cancer. KW - Melanocyte. KW - Melanoma. KW - Zinc finger protein. KW - c-Ret. UR - http://www.scopus.com/inward/record.url?scp=67349128973&partnerID=8YFLogxK. UR - http://www.scopus.com/inward/citedby.url?scp=67349128973&partnerID=8YFLogxK. U2 - 10.1016/j.jdermsci.2009.02.010. DO - 10.1016/j.jdermsci.2009.02.010. M3 - Letter. C2 - 19329283. AN - SCOPUS:67349128973. VL - 55. SP - 68. EP - 70. JO - Journal of Dermatological Science. JF - Journal of Dermatological Science. SN - 0923-1811. IS - 1. ER - ...
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Artificial transcription factors can be engineered to interact with specific DNA sequences to modulate endogenous gene expression within cells. A significant hurdle to implementation of this approach is the selection of the appropriate DNA sequence for targeting. We reasoned that a good target site should be located in chromatin, where it is accessible to DNA-binding proteins, and it should be, in the close vicinity of known transcriptional regulators of the gene. Here we have explored the efficacy of these criteria to guide our selection of potential regulators of gamma-globin expression. Several zinc finger-based transcriptional activators were designed to target the sites proximal to the -117-position of the gamma-globin promoter. This region is proximal to the binding sites of known and potential natural transcription factors. Design and study of three transcription factors identified the potent transcriptional activator, ggl-VP64-RA. This transcription factor was able to interact directly ...
Sangamo BioSciences, Inc. is focused on research and development of novel DNA-binding proteins for therapeutic gene regulation and genome editing. The Company has ongoing Phase 2 clinical trials to evaluate the safety and efficacy of a novel ZFP Therapeutic® for the treatment of HIV/AIDS. Sangamos other therapeutic programs are focused on monogenic diseases, including hemophilia, Huntingtons disease and hemoglobinopathies such as sickle cell anemia and beta-thalassemia. Sangamos core competencies enable the engineering of a class of DNA-binding proteins known as zinc finger DNA-binding proteins (ZFPs). Engineering of ZFPs that recognize a specific DNA sequence enables the creation of sequence-specific ZFP Nucleases (ZFNs) for gene modification and ZFP transcription factors (ZFP TFs) that can control gene expression and, consequently, cell function. Sangamo has entered into a strategic collaboration with Shire AG to develop therapeutics for hemophilia, Huntingtons disease and other monogenic ...
Direct editing of disease-causing mutations has obvious attractions for the treatment of genetic disorders if the many practical obstacles to the technique can be overcome. One promising line of research centres on the development of zinc finger nucleases (ZFNs) produced by fusing an engineered zinc finger DNA-binding domain to an endonuclease. These artificial enzymes induce efficient gene correction in cultured cells. Li et al. now report that zinc finger nucleases induce double-strand breaks in specifically selected locations on the genome and stimulate genome editing at a clinically meaningful level in vivo. In a proof-of-principle experiment, ZFNs delivered to the liver in a mouse model of haemophilia B achieved a level of gene replacement that was sufficient to correct the clotting defect, and the effect persisted following liver regeneration. Editing of the human genome to correct disease-causing mutations is a promising approach for the treatment of genetic disorders. Genome editing improves on
TY - JOUR. T1 - Outlier analysis defines zinc finger gene family DNA methylation in tumors and saliva of head and neck cancer patients. AU - Gaykalova, Daria A.. AU - Vatapalli, Rajita. AU - Wei, Yingying. AU - Tsai, Hua Ling. AU - Wang, Hao. AU - Zhang, Chi. AU - Hennessey, Patrick T.. AU - Guo, Theresa. AU - Tan, Marietta. AU - Li, Ryan. AU - Ahn, Julie. AU - Khan, Zubair. AU - Westra, William H.. AU - Bishop, Justin A.. AU - Zaboli, David. AU - Koch, Wayne M.. AU - Khan, Tanbir. AU - Ochs, Michael F.. AU - Califano, Joseph A.. N1 - Funding Information: The analysis in this article is based on a web database applications provided by Research Information Technology Systems (RITS)-https://www.rits.onc.jhmi.edu/. This work was supported by the National Institute of Dental and Craniofacial Research and National Institute of Health Challenge Grant (RC1DE020324); National Institute of Dental and Craniofacial Research and National Cancer Institute grant (P50 DE 019032 Head and Neck Cancer SPORE) to ...
Spodoptera frugiperda SF-21 cells infected with Autographa californica nuclear polyhedrosis virus mutants which lack a functional p35 gene undergo apoptosis, a type of programmed cell death. To identify p35-homologous genes in other baculoviruses, A. californica nuclear polyhedrosis virus DNA containing a deletion in p35 was cotransfected into SF-21 cells along with genomic DNAs from other baculoviruses. One of the viral DNAs which were able to rescue wild-type infection was from Cydia pomonella granulosis virus (CpGV). The CpGV gene responsible for the effect was mapped to a 1.6-kb SalI-SstI subclone of the SalI B fragment of CpGV. The sequence of the SalI-SstI subclone revealed an open reading frame capable of encoding a polypeptide of 31 kDa which was sufficient to rescue wild-type infection; this gene was thus called iap (inhibitor of apoptosis). The predicted sequence of the IAP polypeptide exhibited no significant homology to P35 but contained a zinc finger-like motif which is also found ...
TY - JOUR. T1 - A zinc finger transcription factor ART1 regulates multiple genes implicated in aluminum tolerance in rice. AU - Yamaji, Naoki. AU - Huang, Chao Feng. AU - Nagao, Sakiko. AU - Yano, Masahiro. AU - Sato, Yutaka. AU - Nagamura, Yoshiaki. AU - Ma, Jian Feng. PY - 2009/10. Y1 - 2009/10. N2 - Aluminum (Al) toxicity is the major limiting factor of crop production on acid soils, but some plant species have evolved ways of detoxifying Al. Here, we report a C2H2-type zinc finger transcription factor ART1 (for Al resistance transcription factor 1), which specifically regulates the expression of genes related to Al tolerance in rice (Oryza sativa). ART1 is constitutively expressed in the root, and the expression level is not affected by Al treatment. ART1 is localized in the nucleus of all root cells. A yeast one-hybrid assay showed that ART1 has a transcriptional activation potential and interacts with the promoter region of STAR1, an important factor in rice Al tolerance. Microarray ...
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Nucleases are the enzyme, used to cleave DNA into smaller units. Zinc-finger (ZFN) nucleases are artificial restriction enzyme used to cleave DNA into smaller fragments. It is the class of engineered DNA-binding proteins that creates double standard break at specified locations. It consist of two functional domain, a DNA-binding domain, and a DNA-cleaving domain. DNA binding domain recognizes the unique hexamer sequence of DNA and DNA-cleaving domain consisting nuclease domain of Fok I. The fusion between the DNA-binding domain, and a DNA-cleaving domain creates artificial restriction enzyme known as molecular scissor that cleaves the desired DNA sequence. ZFN is based on the DNA repair machinery and is becoming a prominent tool in the field of genome editing.. Zinc finger nucleases are useful for various biotechnological and life science applications. It is used to manipulate plants and animals for research purpose and is used in the clinical trial of CD4+ human T-cells for the treatment of ...
The first three zinc fingers (ZF1-3) of transcription factor IIIA (TFIIIA) from Xenopus have been shown to contribute the majority of the binding energy to the intact TFIIIA-DNA interaction [Liao et al. (1992) J. Mel. Biol, 223, 857-871]. We have expressed a 92-amino acid polypeptide containing the three N-terminal zinc fingers of TFIIIA. This three-fingered polypeptide has
CCCH zinc finger alignments in Postia placenta . Alignments can be refined by adding alignments from other genomes, adding your own sequences and/or aligning to other models from the same superfamily. The display of alignments can also be customised.
Krüppel-like factor (KLF) family members share a three C2H2 zinc finger DNA binding domain, and are involved in cell proliferation and differentiation control in normal as in pathological situations. KLFs can be deregulated in multiple cancers either by loss of heterozygosity (LOH), somatic mutation or transcriptional silencing by promoter hypermethylation. KLF family member proteins play a critical role in the growth and metastasis of numerous tumor types, at least in part by regulating the expression of cell cycle genes. Globally, KLF4 and KLF6 are considered as tumor suppressor gene, whereas KLF5 promotes cell proliferation. Family members have different transcriptional properties and can modulate each others activity by a variety of mechanisms. Since cells can express multiple KLFs, KLF transcription factors build likely a transcriptional network to control cell proliferation. Effects of changes in KLF factors are context-dependent and can appear contradictory, considering differences in ...
From NCBI Gene:. In human, ZIM2 and PEG3 are treated as two distinct genes though they share multiple 5 exons and a common promoter and both genes are paternally expressed (PMID:15203203). Alternative splicing events connect their shared 5 exons either with the remaining 4 exons unique to ZIM2, or with the remaining 2 exons unique to PEG3. In contrast, in other mammals ZIM2 does not undergo imprinting and, in mouse, cow, and likely other mammals as well, the ZIM2 and PEG3 genes do not share exons. Human PEG3 protein belongs to the Kruppel C2H2-type zinc finger protein family. PEG3 may play a role in cell proliferation and p53-mediated apoptosis. PEG3 has also shown tumor suppressor activity and tumorigenesis in glioma and ovarian cells. Alternative splicing of this PEG3 gene results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Sep 2009]. From UniProt: ...
GATA-1 and FOG-1 zinc fingers. Computer model showing the complex of the zinc finger transcription factors GATA-1 (orange) and FOG-1 (friend of GATA, blue). The two zinc ions shown in grey become visible after removing a few atoms hiding them. - Stock Image C035/5609
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Transcription factor that mediates a transcriptional program in various innate and adaptive immune tissue-resident lymphocyte T cell types such as tissue-resident memory T (Trm), natural killer (trNK) and natural killer T (NKT) cells and negatively regulates gene expression of proteins that promote the egress of tissue-resident T-cell populations from non-lymphoid organs. Plays a role in the development, retention and long-term establishment of adaptive and innate tissue-resident lymphocyte T cell types in non-lymphoid organs, such as the skin and gut, but also in other nonbarrier tissues like liver and kidney, and therefore may provide immediate immunological protection against reactivating infections or viral reinfection (By similarity). Binds specifically to the PRDI element in the promoter of the beta-interferon gene (PubMed:1851123). Drives the maturation of B-lymphocytes into Ig secreting cells (PubMed:12626569). Associates with the transcriptional repressor ZNF683 to chromatin at gene ...
Genetic analysis and homology between the phenotypic alterations of the human Greig Cephalopolysyndactyly Syndrome (GCPS) and the mouse mutant extra-toes (Xt) have suggested a dominant mutation in the same gene of both species. Recently, the GLI3 gene, a member of the Kruppel-related zinc finger genes, has been proposed as a candidate gene for GCPS. We examined the expression of the mouse Gli3 gene in both Xt mutant animals and during normal mouse development. Northern and RNAase protection analysis of embryos revealed that Gli3 expression was reduced about 50% in heterozygous Xt/+ mice and completely absent in homozygous Xt/Xt mice. In addition, in situ analysis of wild-type mice documented Gli3 expression in the developing limb and brain, structures affected in Xt mutant mice. This pattern suggests an important function of the Gli3 gene during morphogenesis.. ...
National Cancer Institute. Evi3 is a common site of retroviral integration in B-cell lymphomas of AKXD mice. BLAST searches of Evi3 genomic sequences against the mouse and human databases showed that most viral integrations at Evi3 are located immediately upstream of the first translated exon (exon 2) of a gene encoding a novel zinc finger protein with 30 kr ppel-like zinc finger repeats. Viral integrations at Evi3 upregulate the expression of this gene via promoter sequences present in the viral long terminal repeat. EVI3 protein is highly related to the early B-cell associated zinc finger protein EBFAZ, and all 30 zinc fingers found in EVI3 are conserved in EBFAZ. Ebfaz and Evi3 are coexpressed in many cell types, and EVI3, like EBFAZ, is located in the nucleus. EBFAZ binds to, and negatively regulates, early B cell factor (EBF), a basic helix-loop-helix transcription factor required for B-cell-lineage commitment. EBFAZ also binds to SMAD1 and SMAD4 in response to BMP2 signaling, which in turn ...
Education. -1998 PhD (4 years program) at University of Rome La Sapienza in Human Biology: Cellular and Molecular Biology Bases. -1991 Degree in Biology, University of Rome La Sapienza Department of Human Biopathology. University of Rome La Sapienza, Rome, Italy. Experimental Thesis, summa cum laude.. Current position and research experience. -From 2009 to present CNR Researcher (III level) at Istituto Biologia e Patologia Molecolari (IBPM), CNR, Rome, Italy.. -From 1999 to 2008 post-doctoral fellow at CNR, Istituto Biologia e Patologia Molecolari (IBPM), Rome, Italy.. -From 1994 to1998 PhD (4 years program) at University of Rome La Sapienza in Human Biology: Cellular and Molecular Biology Bases. Thesis on artificial zinc finger transcription factors programmed to upregulate utrophin gene in Duchenne Muscular Dystrophy (DMD). Supervisor: Dr. Claudio Passananti.. -From 1995 to 1993 research experience as PhD/fellow in the field of Regulation of gene expression and development in the ...
PubMed Central Canada (PMC Canada) provides free access to a stable and permanent online digital archive of full-text, peer-reviewed health and life sciences research publications. It builds on PubMed Central (PMC), the U.S. National Institutes of Health (NIH) free digital archive of biomedical and life sciences journal literature and is a member of the broader PMC International (PMCI) network of e-repositories.
In order to study the mechanism of neural patterning in Xenopus, we used subtractive cloning to isolate genes activated early during this process. One gene isolated was opl, (odd-paired-like) that resembles the Drosophila pair-rule gene odd-paired and encodes a zinc finger protein that is a member of the Zic gene family. At the onset of gastrulation, opl is expressed throughout the presumptive neural plate, indicating that neural determination has begun at this stage while, by neurula, opl expression is restricted to the dorsal neural tube and neural crest. opl encodes a transcriptional activator, with a carboxy terminal regulatory domain, which when removed increases opl activity. opl both sensitizes animal cap ectoderm to the neural inducer noggin and alters the spectrum of genes induced by noggin, allowing activation of the midbrain marker engrailed. Consistent with the later dorsal neural expression of opl, the activated form of opl is able to induce neural crest and dorsal neural tube ...
Department of Medicine, Vanderbilt University Medical Center, Nashville, Tennessee 37232, USA. The epithelium lining the intestine undergoes rapid and continuous renewal. Growth factors play a role in intestinal epithelial growth regulation in vitro and in vivo. In this study, transforming growth factor alpha (TGF alpha) is shown to act as a mitogen and induce the expression of two zinc finger-containing immediate early genes [Zif268 (zinc finger protein 268) and Nup475 (nuclear protein 475)] in rat intestinal epithelial (RIE-1) cells in culture. These two gene products were initially isolated from serum-treated fibroblasts and represent growth-stimulated transcription factors. In TGF alpha-treated RIE-1 cells, nuclear run-on experiments demonstrate that TGF alpha induction of these two genes is regulated predominantly at the level of gene transcription. Utilizing in situ hybridization techniques, we show that systemic administration of TGF alpha induces expression of these two genes in the rat ...
Exploring the Recognition of Quadruplex DNA by an Engineered Cys2-His2 Zinc Finger Protein. Biochemistry 45 (5) , pp. 1393-1399. 10.1021/bi050229x ...
1CS3: Structure-function studies of the BTB/POZ transcriptional repression domain from the promyelocytic leukemia zinc finger oncoprotein.
The ubiquitin-binding zinc finger (UBZ) is a type of zinc-coordinating β-β-α fold domain found mainly in proteins involved in DNA repair and transcriptional regulation. UBZ domains coordinate a zinc ion with cysteine or histidine residues; depending on their amino acid sequence, UBZ domains are classified into several families [1,2]. Type 1 UBZs are CCHH-type zinc fingers found in tandem UBZ domains of TAX1-binding protein 1 (TAX1BP1) [3,4,5], type 2 UBZs are CCHC-type zinc fingers found in FAAP20 which is a subunit of the Fanconi anemia (FA) core complex [6,7], type 3 UBZs are CCHH-type zinc fingers found only in the Y-family translesion polymerase eta [8,9,10], and type 4 UBZs are CCHC-type zinc fingers found in Y-family translesion polymerase kappa, Werner helicase-interacting protein 1 (WRNIP1), and Rad18 [11,12,13]. The UBZ domain consists of two short antiparallel β-strands followed by one α-helix. The α-helix packs against the β-strands with a zinc ion sandwiched between the ...
Targeted disruption of T cell receptor genes using engineered zinc finger protein nucleases - Disclosed herein are methods and compositions for inactivating TCR genes, using zinc finger nucleases (ZFNs) comprising a zinc finger protein and a cleavage domain or cleavage half-domain in conditions able to preserve cell viability. Polynucleotides encoding ZFNs, vectors comprising polynucleotides encoding ZFNs and cells comprising polynucleotides encoding ZFNs and/or cells comprising ZFNs are also provided. Disclosed herein are also methods and compositions for expressing a functional exogenous TCR in the absence of endogenous TCR expression in T lymphocytes, including lymphocytes with a central memory phenotype. Polynucleotides encoding exogenous TCR, vectors comprising polynucleotides encoding exogenous TCR and cells comprising polynucleotides encoding exogenous TCR and/or cells comprising exogenous TCR are also provided ...
Zinc is an essential trace element that plays a crucial role in catalytic, structural and regulatory functions of many proteins including enzymes and transcription factors; thus maintenance of zinc balance is critical for normal cellular function. Cellular mechanisms that maintain zinc balance include the regulation of genes coding for proteins that play vital roles in zinc homeostasis. These proteins include zinc transporters belonging to the ZIP (SLC39A) and ZnT (SLC30A) families as well as the zinc-binding metallothionein proteins. In contrast to bacterial and yeast systems, a transcription factor responsible for mediating transcriptional repression of a suite of genes in response to elevated zinc levels in mammals has hitherto not been identified. Using Caco-2 cells as a model of human intestinal epithelial cells and detection of protein binding by electrophoretic mobility shift analysis, we show that zinc finger protein ZNF658 binds specifically to the zinc transcriptional regulatory ...
Inhibitor of apoptosis proteins (IAPs) constitute a conserved family of molecules, which regulate both apoptosis and receptor signalling. They are often deregulated in cancer cells and represent potential targets for therapy. In my work, I investigated the effect of IAP inhibition in vivo to identify novel down-stream genes expressed in an IAP-dependent manner that could contribute to cancer aggressiveness. To this end, immunocompromised mice engrafted subcutaneously with the triple negative breast cancer (TNBC) cell line MDA-MB231 were treated with SM83, a Smac mimetic developed in our laboratory that acts as a pan-IAP inhibitor, and tumour nodules were profiled for gene expression. The analysis revealed that the inhibition of IAPs significantly reduces the expression of SNAI2, a zinc finger transcriptional repressor often associated with cancer aggressiveness, resistance to therapy and metastatic potential, especially in breast cancer. By testing several TNBC cell lines, I found that SNAI2 ...
Krüppel-like factor 5 (intestinal) or Krüppel-like factor 5 (KLF5) is a zinc finger-containing transcription factor and involved in important biological processes including cell proliferation and differentiation. However, clinical significance of KLF5 protein has remained largely unknown in breast cancer. Therefore, in this study, we immunolocalized KLF5 in 113 human breast carcinoma cases. KLF5 immunoreactivity was frequently detected in the nuclei of breast carcinoma cells, and median value of the ratio of KLF5-positive carcinoma cells was 30% and was positively associated with the status of androgen receptor. KLF5 immunoreactivity was also significantly associated with increased risk of recurrence and worse clinical outcome in breast cancer patients by univariate analyses, and subsequent multivariate analyses demonstrated that KLF5 immunoreactivity was an independent prognostic factor for both disease-free and breast cancer-specific survival of the patients. We then examined possible regulation of
TY - JOUR. T1 - Finger inter-dependence. T2 - Linking the kinetic and kinematic variables. AU - Kim, Sun Wook. AU - Shim, Jae Kun. AU - Zatsiorsky, Vladimir M.. AU - Latash, Mark L.. N1 - Funding Information: This study was supported in part by NIH Grants AG-018751, AR-048563, and NS-35032.. PY - 2008/6. Y1 - 2008/6. N2 - We studied the dependence between voluntary motion of a finger and pressing forces produced by the tips of other fingers of the hand. Participants moved one of the fingers (task finger) of the right hand trying to follow a cyclic, ramp-like flexion-extension template at different frequencies. The other fingers (slave fingers) were restricted from moving; their flexion forces were recorded and analyzed. Index finger motion caused the smallest force production by the slave fingers. Larger forces were produced by the neighbors of the task finger; these forces showed strong modulation over the range of motion of the task finger. The enslaved forces were higher during the flexion ...
Each competitor and mentor would love to have something that would avoid finger wounds. A torn tendon can prompt to lessen playing time for a competitor. There is additionally the danger of lasting handicap. These conceivable outcomes cause numerous competitors to wear a finger prop practically speaking and even in amusements. Concentrates on have demonstrated that the prophylactic finger support can forestall harm yet there are clashing reports also. The finger is uncovered and exceptionally helpless amid athletic action and in view of its huge size it is frequently harmed. In sports, finger supports have two purposes. They are intended to ensure the competitor with past finger wounds. The finger prop underpins the finger to diminish torment. It likewise keeps the finger from being harmed again as it mends. The prop additionally ensures the finger amid substantial physical games and keeps the finger from being harmed. Browse around this website ...
Dergai, O., Cousin, P., Gouge, J., Satia, K., Praz, V., Kuhlman, T., Lhote, P., Vannini, A., Hernandez, N. (May 2018) Mechanism of selective recruitment of RNA polymerases II and III to snRNA gene promoters. Genes Dev, 32 (9-10). pp. 711-722. ISSN 0890-9369 Denissov, S., Van Driel, M., Voit, R., Hekkelman, M., Hulsen, T., Hernandez, N., Grummt, I., Wehrens, R., Stunnenberg, H. (February 2007) Identification of novel functional TBP-binding sites and general factor repertoires. Embo Journal, 26 (4). pp. 944-954. ISSN 0261-4189 Emran, F., Florens, L., Ma, B., Swanson, S. K., Washburn, M. P., Hernandez, N. (August 2006) A role for Yin Yang-1 (YY1) in the assembly of snRNA transcription complexes. Gene, 377. pp. 96-108. ISSN 0378-1119 (Print) Kim, Y. S., Kim, J. M., Jung, D. L., Kang, J. E., Lee, S., Kim, J. S., Seol, W., Shin, H. C., Kwon, H. S., Van Lint, C., Hernandez, N., Hur, M. W. (June 2005) Artificial zinc finger fusions targeting Sp1-binding sites and the trans-activator-responsive element ...
Author Summary The ability of sexually reproducing organisms to produce viable offspring depends on their ability to faithfully execute meiosis. Meiosis is a specialized set of two cell divisions that ensures that each sperm and egg receives only one copy of each pair of chromosomes. Thus, in human females, although virtually all somatic cells carry 23 pairs of homologous chromosomes (for a total of 46 chromosomes), the egg needs to possess only one copy of each chromosome (for a total of 23). This reduction in chromosome number requires three basic steps: the pairing of homologous chromosomes, the linking of those pairs by recombination, and the separation of those pairs into two daughter cells at the first meiotic division. Unfortunately, little is known about the mechanism(s) by which the sites of recombination are chosen. Here we describe a Drosophila protein called Trem that both binds to meiotic chromosomes and defines the first known step of recombination initiation in Drosophila. Our studies of
hypothetical protein, PAC1, Anapl_07643, AS27_06939, AS28_03976, bcd1, B-cell-derived protein 1, C86813, CB1_000294041, cba1, copeb, core promoter element binding protein, core promoter element-binding protein, cpbp, FM2, FM6, GBF, GC-rich binding factor, GC-rich sites-binding factor GBF, Ierepo1, Ierepo3, immediate early response, erythropoietin 1, klf6-a, klf6-b, Krueppel-like factor 6, Krueppel-like factor 6-like, Krueppel-like factor 7, Kruppel-like factor 6, Kruppel-like zinc finger protein Zf9, M91_01956, M959_03695, MDA_GLEAN10016415, N300_13616, N301_13483, N302_03995, N303_03824, N305_14493, N306_00708, N307_00582, N308_06795, N309_01017, N312_07173, N320_02403, N321_14125, N322_09693, N324_04458, N325_02508, N326_01608, N327_05534, N328_08868, N329_08139, N330_10147, N331_09768, N332_08191, N334_00881, N335_03384, N336_10967, N339_05665, N340_06919, N341_10990, PAL_GLEAN10001872, PANDA_010138, proto-oncogene BCD1, protooncogene B-cell derived 1, R75280, ST12, suppression of ...
Its been a while since weve seen something from Amon Tobins alter ego - Two Fingers, but thats gonna get fixed really soon. A brand new EP. Check out Six Rhythms by Two Fingers, Noisia on Beatport. Two Fingers, the alias of our longtime friend Amon Tobin emerges on Division. Six new tracks including a Noisia feature, pressed on 1 x grams 12 vinyl. Mixmag - Premiere: Two Fingers - Cashew Rhythm (Original) Amon Tobin - Two Fingers - Saint Rhythm [Nest HQ Premiere] Amon Tobin - Two Fingers - Tasm Fet. Two Fingers, the alias of our longtime friend Amon Tobin emerges on Division. Six new tracks including a Noisia feature. Artwork by. View credits, reviews, tracks and shop for the Vinyl release of Six Rhythms on Discogs. Discover releases, reviews, credits, songs, and more about Two Fingers - Six Rhythms at Discogs. Complete your Two Fingers collection. Six Rhythms. By Two Fingers. • 6 songs. Play on Spotify. 1. Cashew Listen to Six Rhythms in full in the Spotify app. Play on Spotify. Playing. ...
ZC3H10 - ZC3H10 (GFP-tagged) - Human zinc finger CCCH-type containing 10 (ZC3H10) available for purchase from OriGene - Your Gene Company.
Notably, under conditions in which no killing of cells occurred, exposure of yeast over hundreds of generations to increasing concentrations of AmB has yielded resistant strains with permanent changes in the expression of genes such as yor1 and pdr16 (41), which are members of the ATP-binding cassette (ABC) family of transporters (9). The activation of yor1 and pdr16 is controlled by the zinc finger transcription factors Pdr1 and Pdr3, which activate proteins involved in multidrug resistance and in the translocation of plasma membrane phospholipids (9). Among the stably overexpressed genes that also confer resistance to AmB (41) are ict1, which encodes a lysophosphatidic acid acyltransferase that is responsible for enhanced phospholipid synthesis and increased resistance to antifungal drugs, and ygr035C and ypl088, which are activated by Yrm1q and Yrr1, the yeast zinc finger transcription factors which are also controlled by the pleiotropic drug resistance (PDR) gene network (9).. Another yeast ...
Buy our Recombinant Human MBD2 Interacting Zinc Finger MIZF protein. Ab161859 is a protein fragment produced in Wheat germ and has been validated in WB, ELISA…
The binding of Au(iii) complexes to the zinc finger domain of the anticancer drug target PARP-1 was studied using a hyphenated mass spectrometry approach combined with quantum mechanics/molecular mechanics (QM/MM) studies. Competition experiments were carried out, whereby each Au complex was exposed to two t
LIM (Lin-1, Isl1, Mec3) domain proteins all contain least one double zinc finger motif (Fig. 1). LIM family proteins contain between one and five LIM domains plus other that have specific functions such as actin-binding, kinases, and nuclear translocation motifs. We are the first to examine 33 LIM proteins (including three that bind to but do not themselves contain LIM domains) that are implicated in either the development of the heart, heart disorders and failure or both.. We then assembled a cellular snapshot of the LIM proteins known to be expressed in the heart that helps explain how mutations in these proteins may play a role in the development of heart failure. Furthermore, we name the complexity of LIM domain protein interactions as a LIM interactome.. ...
Numbness in right index finger - Hi, I have a random, tingling, and numbness to my right index finger at random times of the day. I havent hit my arm or jammed my finger or any sorts? More information. Many possibilities, more information is needed. If one taps on your median nerve in the wrist does your finger tingle. If one puts pressure on the proper digital nerve in the palm or finger can you reproduce the symptoms. If the problem was in a nerve root (C6) you would also get shooting pains to from the neck down to the finger. Time will tell. It will either or worse.
Recent development in gene targeting tools makes production of knockout (KO) rabbits possible. In the present work, we generated five...
The zinc-finger transcription factor Insulinoma-associated 1 (Insm1, previously IA-1) is expressed in the developing anxious and neuroendocrine systems, and is required for cell type specific differentiation. maintained in accordance with established protocols for zebrafish husbandry (Westerfield, 1995). Larvae and Embryos had been housed at 28C, on the 14 h light:10 h dark routine. Fish had been anaesthetized with Ethyl 3-aminobenzoate methanesulfonate sodium (MS-222, Tricaine, Sigma-Aldrich, St. Louis, MO). Embryos had been staged as previously referred to (Kimmel et al., 1995). Crazy type strains included the Ekwill stress (Ekwill Fish Plantation, Gibsonton, FL), the Stomach strain extracted from the Zebrafish International Analysis Middle (ZIRC, Eugene, OR) and hybrids made by crossing the Ekwill and Stomach strains. The Tg MK-0812 (XRho: distance43-mCFP) q13 transgenic range, called XOPS-mCFP hereafter, continues to be previously referred to (Morris et al., 2011; Morris et al., 2008a). This ...
Arsenic, an ancient drug used in traditional Chinese medicine, has attracted wide interest because it has therapeutic activity in patients with acute promyelocytic leukemia (APL). The drug acts by promoting degradation of an oncogenic protein, PML-RARα, a fusion protein containing sequences from the PML zinc finger protein and retinoic acid receptor α, which is found specifically in APL cells and helps drive their growth. Zhang et al. (see the Perspective by Kogan) now explain how arsenic initiates the molecular events leading to PML-RARα degradation. Arsenic was found to bind directly to cysteine residues within zinc finger domains of PML. Arsenic binding then induced oligomerization of PML, which in turn enhanced its association with an enzyme that helps catalyze SUMOylation, a posttranslational modification that can target proteins for degradation.. X.-W. Zhang, X.-J. Yan, Z.-R. Zhou, F.-F. Yang, Z.-Y. Wu, H.-B. Sun, W.-X. Liang, A.-X. Song, V. Lallemand-Breitenbach, M. Jeanne, Q.-Y. ...
Zinc finger (Znf) domains are relatively small protein motifs which contain multiple finger-like protrusions that make tandem contacts with their target molecule. Some of these domains bind zinc, but many do not; instead binding other metals such as iron, or no metal at all. For example, some family members form salt bridges to stabilise the finger-like folds. They were first identified as a DNA-binding motif in transcription factor TFIIIA from Xenopus laevis (African clawed frog), however they are now recognised to bind DNA, RNA, protein and/or lipid substrates [(PUBMED:10529348), (PUBMED:15963892), (PUBMED:15718139), (PUBMED:17210253), (PUBMED:12665246)]. Their binding properties depend on the amino acid sequence of the finger domains and of the linker between fingers, as well as on the higher-order structures and the number of fingers. Znf domains are often found in clusters, where fingers can have different binding specificities. There are many superfamilies of Znf motifs, varying in both ...
Zinc finger (Znf) domains are relatively small protein motifs which contain multiple finger-like protrusions that make tandem contacts with their target molecule. Some of these domains bind zinc, but many do not; instead binding other metals such as iron, or no metal at all. For example, some family members form salt bridges to stabilise the finger-like folds. They were first identified as a DNA-binding motif in transcription factor TFIIIA from Xenopus laevis (African clawed frog), however they are now recognised to bind DNA, RNA, protein and/or lipid substrates [(PUBMED:10529348), (PUBMED:15963892), (PUBMED:15718139), (PUBMED:17210253), (PUBMED:12665246)]. Their binding properties depend on the amino acid sequence of the finger domains and of the linker between fingers, as well as on the higher-order structures and the number of fingers. Znf domains are often found in clusters, where fingers can have different binding specificities. There are many superfamilies of Znf motifs, varying in both ...
In molecular biology the MIZ-type zinc finger domain is a zinc finger-containing protein with homology to the yeast protein, ... Wu L, Wu H, Ma L, Sangiorgi F, Wu N, Bell JR, Lyons GE, Maxson R (July 1997). "Miz1, a novel zinc finger transcription factor ... The name MIZ is derived from Msx-interacting-zinc finger. The crystal structure of S. cerevisiae sumo e3 ligase siz1 containing ...
In molecular biology the MYND-type zinc finger domain is a conserved protein domain. The MYND domain (myeloid, Nervy, and DEAF- ... ETO has been shown to be a co-repressor recruited by the promyelocytic leukemia zinc finger (PLZF) protein. A divergent MYND ... associated acute myeloid leukemia is a corepressor for the promyelocytic leukemia zinc finger protein". Mol. Cell. Biol. 20 (6 ... arranged with an invariant spacing to form a potential zinc-binding motif. Mutating conserved cysteine residues in the DEAF-1 ...
"Entrez Gene: Zinc finger protein 84". Retrieved 2016-02-16. v t e v t e (Genes on human chromosome 12, All stub articles, Human ... Zinc finger protein 84 is a protein that in humans is encoded by the ZNF84 gene. GRCh38: Ensembl release 89: ENSG00000198040 - ...
... is a protein that in humans is encoded by the ZNF263 gene. GRCh38: Ensembl release 89: ENSG00000006194 ... "Entrez Gene: Zinc finger protein 263". Retrieved 2017-01-30. v t e (Articles with short description, Short description matches ...
... is a protein that in humans is encoded by the ZFHX2 gene. It has been implicated in pain insensitivity. ... "Entrez Gene: Zinc finger homeobox 2". Habib AM, Matsuyama A, Okorokov AL, Santana-Varela S, Bras JT, Aloisi AM, et al. ( ...
"Entrez Gene: Zinc finger protein 585B". Retrieved 2016-03-22. v t e v t e (Articles with short description, Short description ... Zinc finger protein 585B is a protein that in humans is encoded by the ZNF585B gene. GRCh38: Ensembl release 89: ...
... is a protein that in humans is encoded by the ZNF506 gene. GRCh38: Ensembl release 89: ENSG00000081665 ... "Entrez Gene: Zinc finger protein 506". Retrieved 2016-02-01. v t e (Articles with short description, Short description matches ...
The FPG IleRS zinc finger domain represents a zinc finger domain found at the C-terminal in both DNA glycosylase/AP lyase ... "Mutation of the carboxy terminal zinc finger of E. coli isoleucyl-tRNA synthetase alters zinc binding and aminoacylation ... An Fpg-type zinc finger is also found at the C terminus of isoleucyl tRNA synthetase (EC). This enzyme catalyses the attachment ... The two DNA-binding motifs (a zinc finger and the helix-two-turns-helix motifs) suggest that the oxidized base is flipped out ...
... is a protein that in humans is encoded by the ZNF749 gene. GRCh38: Ensembl release 89: ENSG00000186230 ... "Entrez Gene: Zinc finger protein 749". Retrieved 2016-07-18. v t e (Articles with short description, Short description matches ... Wikidata, Genes on human chromosome 19, All stub articles, Human chromosome 19 gene stubs, Zinc finger proteins). ...
... is a protein that in humans is encoded by the ZNF696 gene. GRCh38: Ensembl release 89: ENSG00000185730 ... "Entrez Gene: Zinc finger protein 696". Retrieved 2016-01-19. v t e (Articles with short description, Short description matches ...
... is a protein that in humans is encoded by the ZNF684 gene. GRCh38: Ensembl release 89: ENSG00000117010 ... "Entrez Gene: Zinc finger protein 684". Retrieved 2016-04-11. v t e (Articles with short description, Short description matches ...
... is a protein that in humans is encoded by the ZNF414 gene. GRCh38: Ensembl release 89: ENSG00000133250 ... "Entrez Gene: Zinc finger protein 414". Retrieved 2016-08-22. v t e (Articles with short description, Short description matches ...
... is a protein that in humans is encoded by the ZNF236 gene. GRCh38: Ensembl release 89: ENSG00000130856 ... "Entrez Gene: Zinc finger protein 236". Holmes DI, Abdel Wahab N, Mason RM (September 1997). "Identification of glucose- ... "The Kruppel-like zinc-finger gene ZNF236 is alternatively spliced and excluded as susceptibility gene for diabetic nephropathy ... a glucose-regulated Kruppel-like zinc-finger gene mapping to human chromosome 18q22-q23". Genomics. 60 (1): 105-9. doi:10.1006/ ...
In molecular biology, the Btk-type zinc finger or Btk motif (BM) is a conserved zinc-binding motif containing conserved ... The Btk motif contains a conserved His and three Cys residues that form a zinc finger (although these differ from known zinc ... Proteins known to contain a Btk-type zinc finger include: Mammalian Bruton's tyrosine kinase (Btk), a protein tyrosine kinase ... The crystal structures of Btk show that the Btk-type zinc finger has a globular core, formed by a long loop which is held ...
... is a protein that in humans is encoded by the ZNF608 gene. GRCh38: Ensembl release 89: ENSG00000168916 ... "Entrez Gene: Zinc finger protein 608". Speliotes EK, Willer CJ, Berndt SI, Monda KL, Thorleifsson G, Jackson AU, et al. ( ...
... is a protein that in humans is encoded by the ZNF439 gene. "Human PubMed Reference:". National Center ... "Entrez Gene: Zinc finger protein 439". Retrieved 2016-03-21. v t e (Articles with short description, Short description matches ...
... is a protein that in humans is encoded by the ZNF134 gene. GRCh38: Ensembl release 89: ENSG00000213762 ... "Entrez Gene: Zinc finger protein 134". Retrieved 2016-01-19. v t e (Articles with short description, Short description matches ...
... is a protein that in humans is encoded by the ZNF780A gene. ENSG00000280568 GRCh38: Ensembl release 89 ... "Entrez Gene: Zinc finger protein 780A". Retrieved 2017-04-14. v t e (Articles with short description, Short description matches ...
... is a protein that in humans is encoded by the ZNF541 gene. GRCh38: Ensembl release 89: ENSG00000118156 ... "Entrez Gene: Zinc finger protein 541". Retrieved 2016-02-11. v t e (Articles with short description, Short description matches ...
... is a protein that in humans is encoded by the ZNF334 gene. This gene encodes a member of the C2H2 zinc ... "Entrez Gene: Zinc finger protein 334". Retrieved 2016-03-10. Henc I, Soroczyńska-Cybula M, Bryl E, Witkowski JM (2015). "The in ... The encoded protein contains a Krueppel-associated box, fourteen C2H2 zinc finger domains, and four C2H2-type/integrase DNA- ... vitro modulatory effect of TNFα on the mRNA expression and protein levels of zinc finger protein ZNF334 in CD4(+) lymphocytes ...
"Entrez Gene: Zinc finger protein 716". Retrieved 2016-02-24. v t e v t e (Genes on human chromosome 7, Human proteins, All stub ... Zinc finger protein 716 is a protein that in humans is encoded by the ZNF716 gene. GRCh38: Ensembl release 89: ENSG00000182111 ...
"Entrez Gene: Zinc finger protein 286A". Retrieved 2017-04-14. v t e (Genes on human chromosome, All stub articles, Human ... Zinc finger protein 286A is a protein encoded in humans by the ZNF286A gene. GRCm38: Ensembl release 89: ENSMUSG00000047342 - ...
... is a protein that in humans is encoded by the ZNF780B gene. ENSG00000281601 GRCh38: Ensembl release 89 ... "Entrez Gene: Zinc finger protein 780B". Retrieved 2016-04-21. v t e (Articles with short description, Short description matches ...
... is a protein that in humans is encoded by the ZNF26 gene. GRCh38: Ensembl release 89: ENSG00000198393 - ... "Entrez Gene: Zinc finger protein 26". Retrieved 2016-02-01. v t e (Genes on human chromosome 12, All stub articles, Human ...
"Entrez Gene: ZFP69 zinc finger protein". Retrieved 2016-02-17. v t e v t e (Articles with short description, Short description ... ZFP69 zinc finger protein is a protein that in humans is encoded by the ZFP69 gene. GRCh38: Ensembl release 89: ENSG00000187815 ...
"Entrez Gene: Zinc finger protein 577". Retrieved 2016-03-04. Sehrawat B, Sridharan M, Ghosh S, Robson P, Cass CE, Mackey JR, ... Zinc finger protein 577 is a protein that in humans is encoded by the ZNF577 gene. GRCh38: Ensembl release 89: ENSG00000161551 ...
... is a protein that in humans is encoded by the ZNF117 gene. GRCh38: Ensembl release 89: ENSG00000152926 ... "Entrez Gene: Zinc finger protein 117". Retrieved 2016-03-22. Rose JE, Behm FM, Drgon T, Johnson C, Uhl GR (2010). "Personalized ...
"Entrez Gene: Zinc finger protein 394". Retrieved 2016-03-02. Huang C, Wang Y, Li D, Li Y, Luo J, Yuan W, Ou Y, Zhu C, Zhang Y, ... Zinc finger protein 394 is a protein that in humans is encoded by the ZNF394 gene. GRCh38: Ensembl release 89: ENSG00000160908 ... Wang Z, Liu M, Wu X (2004). "Inhibition of transcriptional activities of AP-1 and c-Jun by a new zinc finger protein ZNF394". ...
... is a protein that in humans is encoded by the ZNF516 gene. Zinc-finger proteins bind nucleic acids and ... This gene encodes a zinc-finger protein, and belongs to the Krüppel C2H2-type zinc-finger protein family. It may be involved in ... "Entrez Gene: Zinc finger protein 516". Shaffer JR, Feingold E, Wang X, Lee M, Tcuenco K, Weeks DE, Weyant RJ, Crout R, McNeil ...
... is a protein that in humans is encoded by the ZNF786 gene. GRCh38: Ensembl release 89: ENSG00000197362 ... "Entrez Gene: Zinc finger protein 786". Retrieved 2016-03-22. v t e (Genes on human chromosome 7, Human proteins, All stub ...
Gommans WM, Haisma HJ, Rots MG (December 2005). "Engineering zinc finger protein transcription factors: the therapeutic ...
The signature of the C2H2-type zinc finger domain is: C-x(2,4)-C-x(3)-[LIVMFYWC]-x(8)-H-x(3,5)-H A matrix of numbers containing ...
... and zinc cames (instead of the traditional lead) for his leadlight windows, and he famously used Pyrex glass tubing as a major ... All are in my fingers to this day... " In 1881, soon after Wright turned 14, his parents separated. In 1884, his father sued ...
Zinc finger E-box-binding homeobox 2) and PRKD3 (Serine/threonine-protein kinase D3). Neault et al. recently identified miR-137 ...
Towards the latter part of the 19th and early 20th century, some were cast with zinc, commonly referred to as White Bronze. A ... Often, the opposite arm is raised with the index finger of the hand pointing towards the sky. This symbolizes the pathway to ...
ZNF598 is a zinc finger protein and the value is .13. It plays a key role in ribosome quality control. The predicted structures ...
... is a protein that in humans is encoded by the ZNF695 gene. ZNF692 GRCh38: Ensembl release 89: ... "Entrez Gene: Zinc finger protein 695". Retrieved 2016-02-29. Takahashi T, Yamahsita S, Matsuda Y, Kishino T, Nakajima T, ... "Splice variants of zinc finger protein 695 mRNA associated to ovarian cancer". J Ovarian Res. 6 (1): 61. doi:10.1186/1757-2215- ...
... zinc fingers'. In its regulatory role, zinc is involved in the regulation of nucleoproteins and the activity of various ... Zinc deficiency is defined either as insufficient zinc to meet the needs of the body, or as a serum zinc level below the normal ... Even with zinc-efficient varieties, zinc fertilizers are needed when the available zinc in the topsoil becomes depleted. Plant ... As biosystems are unable to store zinc, regular intake is necessary. Excessively low zinc intake can lead to zinc deficiency, ...
... is a protein that in humans is encoded by the ZNF275 gene. This gene encodes a zinc finger protein that ... "Entrez Gene: Zinc finger protein 275". Retrieved 2016-05-31. This article incorporates text from the United States National ...
Such elements include germanium, zinc, platinum, silicon, and boron. Recent examples of these alloys include argentium, ... when etiquette dictated no food should be touched with one's fingers. Serving pieces were often elaborately decorated and ...
Mol Cell Biol 10:3562-3568 (1990) Novel zinc finger gene implicated as myc collaborator by retrovirally accelerated lymphoma ...
YY1 is a zinc-finger protein that acts as a transcriptional repressor for a wide-variety of genes essential for development and ...
Runx2 (which may also be known as Cbfa1), and Osx (a zinc finger containing transcription factor) are necessary for ...
Zinc finger protein GLI2 also known as GLI family zinc finger 2 is a protein that in humans is encoded by the GLI2 gene. The ... Gli family zinc finger proteins are mediators of Sonic hedgehog (Shh) signaling and they are implicated as potent oncogenes in ... GLI2 belongs to the C2H2-type zinc finger protein subclass of the Gli family. Members of this subclass are characterized as ... "Entrez Gene: GLI family zinc finger 2". Tojo M, Kiyosawa H, Iwatsuki K, Nakamura K, Kaneko F (May 2003). "Expression of the ...
Hu HM, Arcinas M, Boxer LM (March 2002). "A Myc-associated zinc finger protein-related factor binding site is required for the ...
The mouse PRC2 has four subunits: Suz12 (zinc finger), Eed, Ezh1 or Ezh2 (SET domain with histone methyltransferase activity) ...
It interacts with HIV-1 Gag protein through Zinc Finger of HIV-1 Gag. GRCh38: Ensembl release 89: ENSG00000147604 - Ensembl, ... Witte S, Krawinkel U (August 1997). "Specific interactions of the autoantigen L7 with multi-zinc finger protein ZNF7 and ... "Specific interactions of the autoantigen L7 with multi-zinc finger protein ZNF7 and ribosomal protein S7". The Journal of ...
"Entrez Gene: ZNF193 zinc finger protein 193". Rual JF, Venkatesan K, Hao T, et al. (2005). "Towards a proteome-scale map of the ... Zinc finger protein 193 is a protein that in humans is encoded by the ZNF193 gene. GRCh38: Ensembl release 89: ENSG00000137185 ... 1997). "Three genes encoding zinc finger proteins on human chromosome 6p21.3: members of a new subclass of the Kruppel gene ... Williams AJ, Blacklow SC, Collins T (2000). "The Zinc Finger-Associated SCAN Box Is a Conserved Oligomerization Domain". Mol. ...
... using zinc-finger nuclease technology, are being commercialized by SAGE Labs. Laboratory mouse Animal testing on rodents Morris ...
The protein, which contains a C2-C2 zinc finger-like domain that can bind to zinc, can enhance the tumor suppressor activity of ...
Zinc finger protein Rlf is a protein that in humans is encoded by the RLF gene. GRCh38: Ensembl release 89: ENSG00000117000 - ... 1996). "The rearranged L-myc fusion gene (RLF) encodes a Zn-15 related zinc finger protein". Oncogene. 11 (12): 2699-704. PMID ...
Zinc finger protein Gfi-1 is a transcriptional repressor that in humans is encoded by the GFI1 gene. It is important normal ... Zweidler-Mckay PA, Grimes HL, Flubacher MM, Tsichlis PN (1996). "Gfi-1 encodes a nuclear zinc finger protein that binds DNA and ... encoding a novel zinc finger protein reveals a new syntenic region between man and rodents". Cytogenet Cell Genet. 70 (3-4): ... "The zinc finger protein Gfi-1 can enhance STAT3 signaling by interacting with the STAT3 inhibitor PIAS3". EMBO J. 19 (21): 5845 ...
This gene encodes a member of the RING zinc finger protein family found in striated muscle and iris. The product of this gene ... Dai KS, Liew CC (June 2001). "A novel human striated muscle RING zinc finger protein, SMRZ, interacts with SMT3b via its RING ... Kedar V, McDonough H, Arya R, Li HH, Rockman HA, Patterson C (December 2004). "Muscle-specific RING finger 1 is a bona fide ... MuRF1 is the name most commonly used in the literature, and it stands for "Muscle RING Finger 1." Structurally, there are two ...
... bric-a-brac/poxvirus and zinc finger (BTB/POZ) domains, which is atypical of CNC-bZip family members. These BTB/POZ domains ...
C) DNA-binding domain (DBD): Highly conserved domain containing two zinc fingers that binds to specific sequences of DNA called ... a novel zinc finger motif (CHC2) is identified in parasitic flatworm NRs. (D) Hinge region: Thought to be a flexible domain ... "Nuclear receptors from the ctenophore Mnemiopsis leidyi lack a zinc-finger DNA-binding domain: lineage-specific loss or ...
It consists of binding sites for fork head domain factors and zinc finger transcription factors. TMEM125 has two variant ...
Tyrosine-protein kinase, or Bromodomain adjacent to zinc finger domain, 1B (BAZ1B) is an enzyme that in humans is encoded by ... "Entrez Gene: BAZ1B bromodomain adjacent to zinc finger domain, 1B". Zanella M, Vitriolo A, Andirko A, Martins PT, Sturm S, ... Pascual J, Martinez-Yamout M, Dyson HJ, Wright PE (December 2000). "Structure of the PHD zinc finger from human Williams-Beuren ...
... and a ZZ-type zinc finger motif. This is likely involved in protein binding, and has recently been identified as a SUMOylation ... "DNA damage-inducible SUMOylation of HERC2 promotes RNF8 binding via a novel SUMO-binding Zinc finger". The Journal of Cell ... Lehman AL, Nakatsu Y, Ching A, Bronson RT, Oakey RJ, Keiper-Hrynko N, Finger JN, Durham-Pierre D, Horton DB, Newton JM, Lyon MF ... At the site of doubles stranded breaks, HERC2 facilitates the binding of RNF8, a RING finger ubiquitin ligase to the E2 ...
... is a protein in humans that is encoded by the GZF1 gene. GRCh38: Ensembl release 89: ... "Entrez Gene: GDNF-inducible zinc finger protein 1". Retrieved 2013-05-28. v t e (Articles with short description, Short ...
... and the multivalent zinc finger factor, CTCF". J. Biol. Chem. 275 (38): 29915-21. doi:10.1074/jbc.M001538200. PMID 10906122. ... "RBBP6 interacts with multifunctional protein YB-1 through its RING finger domain, leading to ubiquitination and proteosomal ...
The KOX zinc finger genes: genome wide mapping of 368 ZNF PAC clones with zinc finger gene clusters predominantly in 23 ... zinc finger protein 20provided by HGNC. Primary source. HGNC:HGNC:12992 See related. Ensembl:ENSG00000132010 MIM:194557; ... The zinc finger-associated SCAN box is a conserved oligomerization domain. Williams AJ, et al. Mol Cell Biol, 1999 Dec. PMID ... Multiple genes encoding zinc finger domains are expressed in human T cells. Thiesen HJ. New Biol, 1990 Apr. PMID 2288909 ...
zinc finger nuclease. NHEJ. nonhomologous end-joining. HR. homologous recombination. KO. knockout. P-gp. P-glycoprotein. MDR/ ... The development of zinc finger nuclease (ZFN) technology has enabled the genetic engineering of the rat genome. The ability to ... Characterization of Multidrug Resistance 1a/P-Glycoprotein Knockout Rats Generated by Zinc Finger Nucleases. Xiaoyan Chu, Zuo ... Characterization of Multidrug Resistance 1a/P-Glycoprotein Knockout Rats Generated by Zinc Finger Nucleases ...
Compare Anti-zinc finger protein 874b Antibody Products from leading suppliers on Biocompare. View specifications, prices, ...
Solution structure of the third zinc finger domain of FOG-1 ... Zinc finger protein ZFPM1. A. 35. Mus musculus. Mutation(s): 3 ... Classic zinc finger domains (cZFs) consist of a beta-hairpin followed by an alpha-helix. They are among the most abundant of ... Classic zinc finger domains (cZFs) consist of a beta-hairpin followed by an alpha-helix. They are among the most abundant of ... A Classic Zinc Finger from Friend of GATA Mediates an Interaction with the Coiled-coil of Transforming Acidic Coiled-coil 3.. ...
View mouse Gatad2a Chr8:70359726-70449034 with: phenotypes, sequences, polymorphisms, proteins, references, function, expression
The zinc finger transcription factor 191 is required for early embryonic development and cell proliferation. Li, J., Chen, X., ... Chromosomal localization of two human zinc finger protein genes, ZNF24 (KOX17) and ZNF29 (KOX26), to 18q12 and 17p13-p12, ... Molecular cloning of six novel Krüppel-like zinc finger genes from hematopoietic cells and identification of a novel ... Establishment of transgenic mice carrying gene encoding human zinc finger protein 191. Li, J.Z., Chen, X., Yang, H., Wang, S.L ...
Timeline for Protein Zinc finger FYVE domain-containing protein 19 from g.43.1.1: B-box zinc-binding domain: *Protein Zinc ... Protein Zinc finger FYVE domain-containing protein 19 from g.43.1.1: B-box zinc-binding domain appears in SCOPe 2.07. ... More info for Protein Zinc finger FYVE domain-containing protein 19 from g.43.1.1: B-box zinc-binding domain. ... Lineage for Protein: Zinc finger FYVE domain-containing protein 19. *Root: SCOPe 2.08 *. Class g: Small proteins [56992] (100 ...
The human zinc finger antiviral protein (ZAP) is capable of inhibiting several major human pathogens, including Influenza A ... The human zinc finger antiviral protein (ZAP) is capable of inhibiting several major human pathogens, including Influenza A ... Role and modulation of Zinc-finger antiviral protein and antiviral Regnase-1-like endonucleases. ...
First-in-human in vivo genome editing via AAV-zinc finger nucleases for mucopolysaccharidosis I/II and hemophilia B ... Non-viral Delivery of Zinc Finger Nuclease mRNA Enables Highly Efficient In Vivo Genome Editing of Multiple Therapeutic Gene ... Diversifying the structure of zinc finger nucleases for high-precision genome editing ...
Engineered zinc finger protein transcription factors (ZFP TFs) can be designed to specifically increase the level of a ... Engineered zinc finger protein transcription factors (ZFP TFs) can be designed to specifically increase the level of a ... Develop Engineered Zinc Finger Protein Transcriptional Activators of the Glial Cell Line-Derived Neurotrophic Factor (GDNF) ... Development of a Zinc Finger Protein Therapeutic for the Potential Treatment of Parkinsons Disease ...
Some compounds were also screened for their inhibitory effect of the zinc-finger protein. PARP-1, essential for DNA repair and ... biological characterization and investigation of their inhibition properties of the zinc finger protein. PARP-1 M. Serratrice, ... biological characterization and investigation of their inhibition properties of the zinc finger protein PARP-1† ...
A team of researchers lead by Huanzhang Zhu used the on target DNA cleaving potential of zinc finger nucleases to cleave the ... To do this they targeted zinc finger-FokI fusions to a sequence within the extremely well conserved long terminal repeat (LTR) ... In fact, a team of researchers lead by Huanzhang Zhu used the on target DNA cleaving potential of zinc finger nucleases to ... The team concluded that the use of their designed zinc finger as part of a therapeutic strategy, could indeed eradicate the ...
Zinc finger proteins: New insights into structural and functional diversity. Curr. Opin. Struct. Biol. 2001; 11:39-46. ... Zinc finger proteins as designer transcription factors. J. Biol. Chem. 2000; 275:8742-8. ... Adaptive evolution in zinc finger transcription factors. PLoS Genet. 2009; 5:e1000325. ... Analysis of an artificial zinc finger epigenetic modulator: widespread binding but limited regulation. Nucleic Acids Res. 2014 ...
We derived the modeling approach for generating a three-Cys2His2 zinc-finger-DNA complex model according to the results of ... Our docking data demonstrate that two AIRs with a reasonable geometric distribution in each of the three-Cys2His2 zinc-finger ... This approach is efficient for generating a zinc-finger protein-DNA complex model for unknown complex structures in which the ... Defining the ambiguous interaction restraints for the classical three-Cys2His2 zinc-finger proteins that wrap around DNA is ...
Dive into the research topics of The T-Box near the Zinc Fingers of the Human Vitamin D Receptor Is Required for Heterodimeric ... The T-Box near the Zinc Fingers of the Human Vitamin D Receptor Is Required for Heterodimeric DNA Binding and Transactivation. ...
Lu, Yan, "The Role of Thylakoid Zinc-Finger Proteins in Photosynthesis" (2014). Faculty Research and Creative Activities Award ...
title = "Chromosomal localization of four human zinc finger cDNAs",. abstract = "cDNA clones encoding zinc finger motifs were ... cDNA clones encoding zinc finger motifs were isolated by screening human placenta and T-cell (Peer) cDNA libraries with zinc ... cDNA clones encoding zinc finger motifs were isolated by screening human placenta and T-cell (Peer) cDNA libraries with zinc ... cDNA clones encoding zinc finger motifs were isolated by screening human placenta and T-cell (Peer) cDNA libraries with zinc ...
Identification of a novel TGF-β-regulated gene encoding a putative zinc finger protein in human osteoblasts. In: Nucleic acids ... Identification of a novel TGF-β-regulated gene encoding a putative zinc finger protein in human osteoblasts. Nucleic acids ... Dive into the research topics of Identification of a novel TGF-β-regulated gene encoding a putative zinc finger protein in ... The TIEG protein contains three zinc finger motifs, several proline-rich src homology-3 (SH3) binding domains at the C-terminal ...
In this complex, the zinc fingers bind in the major groove of B-DNA and wrap part way around the double helix. Each finger has ... This is the protein part of a two-part zinc finger mold, where the DNA model binds into the Zn Model. This is a nested model ... The zinc finger DNA-binding motif occurs in many proteins that regulate eukaryotic gene expression. The crystal structure of a ... This structure provides a framework for understanding how zinc fingers recognize DNA and suggests that this motif may provide a ...
RNA binding by the Wilms tumor suppressor zinc finger proteins. A A Caricasole, Antonio Duarte, S H Larsson, N D Hastie, M ... Dive into the research topics of RNA binding by the Wilms tumor suppressor zinc finger proteins. Together they form a unique ...
Phenotype data for mouse gene Zfp566. Discover Zfp566s significant phenotypes, expression, images, histopathology and more. Data for gene Zfp566 is all freely available for download.
We show by cloning the id1 gene that it encodes a protein with zinc finger motifs, suggesting that the id1 gene product ... The indeterminate gene encodes a zinc finger protein and regulates a leaf-generated signal required for the transition to ... Colasanti, J., Yuan, Z., Sundaresan, V. (1998-05-15). The indeterminate gene encodes a zinc finger protein and regulates a leaf ...
Zinc Finger Design AI Tool Opens Door to Large-Scale Gene Therapies ... Zinc Finger Design AI Tool Opens Door to Large-Scale Gene Therapies. ...
"PHD Zinc Fingers" by people in this website by year, and whether "PHD Zinc Fingers" was a major or minor topic of these ... Zinc finger domains of approximately 50 to 80 amino acids in length that are characterized by a conserved Cysteine(3)-Histidine ... "PHD Zinc Fingers" is a descriptor in the National Library of Medicines controlled vocabulary thesaurus, MeSH (Medical Subject ... Below are the most recent publications written about "PHD Zinc Fingers" by people in Profiles. ...
The KRAB-zinc finger proteins (KRAB-ZFPs) represent a very large, but poorly understood, family of transcriptional regulators ... KRAB zinc-finger proteins localise to novel KAP1-containing foci that are adjacent to PML nuclear bodies. ... View more ,The KRAB-zinc finger proteins (KRAB-ZFPs) represent a very large, but poorly understood, family of transcriptional ...
Comparison of KRC protein zinc finger domains. The zinc finger amino acid sequences of the KRC ZAS domains are compared. Mouse ... The zinc finger 1 and zinc finger 2 domains within the ZAS domains are designated in green and blue font, respectively, in the ... and at position 2 of the second zinc finger (outlined in gray). The linker region between the two zinc fingers is outlined in ... between the first and second zinc fingers of the ZAS-N and ZAS-C domains except at position 3 of the first zinc finger ( ...
Our results demonstrate that expression of the tumor suppressor promyelocytic leukemia zinc finger (PLZF) is decreased in GC ... Our results demonstrate that expression of the tumor suppressor promyelocytic leukemia zinc finger (PLZF) is decreased in GC ... Extracellular vesicle derived miR-544 downregulates expression of tumor suppressor promyelocytic leukemia zinc finger resulting ... Extracellular vesicle derived miR-544 downregulates expression of tumor suppressor promyelocytic leukemia zinc finger resulting ...
Of the 18 zinc fingers contained within ZFP100, the region encompassing fingers 2-6 is sufficient to maintain CB localization. ... Of the 18 zinc fingers contained within ZFP100, the region encompassing fingers 2-6 is sufficient to maintain CB localization. ... Of the 18 zinc fingers contained within ZFP100, the region encompassing fingers 2-6 is sufficient to maintain CB localization. ... Of the 18 zinc fingers contained within ZFP100, the region encompassing fingers 2-6 is sufficient to maintain CB localization. ...
Zinc-Finger Nucleases Induced by HIV-1 Tat Excise HIV-1 From the Host Genome in Infected and Latently Infected Cells. Mol Ther ... Zinc Finger Nuclease. In a preliminary study, ZFN-modified CD4+ T cells with disruption of CCR5 were engrafted into NOD/SCID/ ... Zinc-Finger Nuclease Editing of Human Cxcr4 Promotes HIV-1 Cd4(+) T Cell Resistance and Enrichment. Mol Ther (2012) 20(4):849- ... Simultaneous Zinc-Finger Nuclease Editing of the HIV Coreceptors Ccr5 and Cxcr4 Protects CD4+ T Cells From HIV-1 Infection. ...
2021 , In Memory of Dr. Olusola Akinyele. By Alphegaservices ...
  • The zinc finger DNA-binding motif occurs in many proteins that regulate eukaryotic gene expression. (nih.gov)
  • PHD fingers occur in many proteins that function in chromatin-mediated gene expression and EPIGENETICS such as POLYCOMB-GROUP PROTEINS. (jefferson.edu)
  • The KRAB-zinc finger proteins (KRAB-ZFPs) represent a very large, but poorly understood, family of transcriptional regulators in mammals. (edu.au)
  • Within these chimeric proteins, the DNA binding specificity of the zinc finger protein determines the site of nuclease action.Once the engineered ZFNs recognize and bind to their specified locus, it leads to the dimerization of the two nuclease domains on the ZFNs to evoke a double-strand break (DSB) in the targeted DNA. (wustl.edu)
  • Finger like and finger proteins are like zinc fingers small proteins with a structural motif that is characterized by the coordination of one or more zinc ions in order to stabilize the fold. (blimp-1.com)
  • Motifs in DNA - and RNA-binding proteins whose amino acids are folded into a single structural unit around a zinc atom. (bvsalud.org)
  • argylesock says… Zinc finger nucleases (ZFN) are proteins which can be used in genetic modification (GM, genetic engineering, GE). (wordpress.com)
  • The association is referring to zinc finger nucleases (ZFNs), a class of engineered DNA-binding proteins that facilitate targeted editing of the genome by creating double-strand breaks in DNA at user-specified locations. (wordpress.com)
  • YY1 is a ubiquitously distributed transcription factor belonging to the GLI-Kruppel class of zinc finger proteins. (abbkine.com)
  • Adjustments in the manifestation of transcription elements like Zinc finger E-box-binding homeobox 1/2 (ZEB1/2), Zinc finger proteins SNAIL1 (SNAIL), Twist-related proteins 1 (TWIST) or vimentin (VIM) might become prognostic factors along the way of carcinogenesis [16]. (cancerhugs.com)
  • In fact, a team of researchers lead by Huanzhang Zhu used the on target DNA cleaving potential of zinc finger nucleases to cleave the HIV-1 provirus out of infected human T-cells. (epigenie.com)
  • A significant advancement toward this objective was achieved with the advent of a novel technology that enables high-frequency and high-fidelity genome editing via the application of custom designed zinc finger nucleases (ZFNs). (wustl.edu)
  • Human hematopoietic stem/progenitor cells modified by zinc-finger nucleases targeted to CCR5 control HIV-1 in vivo. (nature.com)
  • In one case zinc finger nucleases were used to delete the CCR5 gene in a patient's cells, a procedure that we discussed in TWiV #278 . (virology.ws)
  • Modification of existing genes in living animal and human cells is enabled by engineered nucleases such as meganucleases, zinc finger nucleases, transcription activator-like effector-based nucleases, and the CRISPR-Cas system. (cdc.gov)
  • Early methods for targeting DSB-inducing nucleases to specific genomic sites relied on protein-based systems with customizable DNA-binding specificities such as meganucleases, zinc finger nucleases (ZFNs) and transcription activator-like effector nucleases (TALENs). (cdc.gov)
  • We established a broadly applicable strategy using zinc finger nucleases (ZFNs) and transcription activator-like effector nucleases (TALENs) for targeted disruption of endogenous genes and cis-acting regulatory elements in diverged nematode species. (bioseek.eu)
  • The development of zinc finger nuclease (ZFN) technology has enabled the genetic engineering of the rat genome. (aspetjournals.org)
  • However, they also stress that delivery of these gene-editing tools in clinical settings remains a pickle, but propose a strategy of transplanted autologous CD34+ cells pretreated with zinc-finger nuclease as the way to go. (epigenie.com)
  • Generation of Esr1-knockout rats using zinc finger nuclease-mediated genome editing. (childrensmercy.org)
  • This entry was posted in agriculture , horticulture , knowledge transfer and tagged biotechnology , crop , crop variety , genetic modification , law , zinc finger nuclease . (wordpress.com)
  • cDNA clones encoding zinc finger motifs were isolated by screening human placenta and T-cell (Peer) cDNA libraries with zinc finger (ZNF) consensus sequences. (elsevier.com)
  • The TIEG protein contains three zinc finger motifs, several proline-rich src homology-3 (SH3) binding domains at the C-terminal end, and is homologous in this region to the zinc finger-containing transcription factor family of genes. (elsevier.com)
  • We show by cloning the id1 gene that it encodes a protein with zinc finger motifs, suggesting that the id1 gene product functions as a transcriptional regulator of the floral transition. (nus.edu.sg)
  • Zinc finger (Znf) domains are relatively small protein motifs which contain multiple finger-like protrusions that make tandem contacts with their target molecule. (embl.de)
  • Zinc-binding motifs are stable structures, and they rarely undergo conformational changes upon binding their target. (embl.de)
  • Zinc finger domains of approximately 50 to 80 amino acids in length that are characterized by a conserved Cysteine(3)-Histidine-Cysteine(4) amino acid motif which coordinates binding of two zinc ions. (jefferson.edu)
  • A ZFN is a chimeric protein that consists of the non-specific endonuclease domain of FokI fused to a DNA-binding domain composed of an engineered zinc-finger motif. (wustl.edu)
  • In the proposed "zinc finger" DNA-binding motif, each repeat unit binds a zinc metal ion through invariant Cys and His residues and this drives the folding of each 30-residue unit into an independent nucleic acid-binding domain. (embl.de)
  • By variations in the composition of the sequences in the fingertip and the number and spacing of tandem repeats of the motif, zinc fingers can form a large number of different sequence specific binding sites. (bvsalud.org)
  • U2 small nuclear ribonucleoprotein auxiliary factor 35 kDa subunit- related protein 2 (U2(RNU2) small nuclear RNA auxiliary factor 1-like 2) (CCCH type zinc finger, RNA-binding motif and serine/arginine rich protein 2) (Renal carcinoma antigen NY-REN-20). (yellowcouch.org)
  • The KOX zinc finger genes: genome wide mapping of 368 ZNF PAC clones with zinc finger gene clusters predominantly in 23 chromosomal loci are confirmed by human sequences annotated in EnsEMBL. (nih.gov)
  • Chromosomal localization of 9 KOX zinc finger genes: physical linkages suggest clustering of KOX genes on chromosomes 12, 16, and 19. (nih.gov)
  • Multiple genes encoding zinc finger domains are expressed in human T cells. (nih.gov)
  • Molecular cloning of six novel Krüppel-like zinc finger genes from hematopoietic cells and identification of a novel transregulatory domain KRNB. (wikigenes.org)
  • hunchback and Ikaros-like zinc finger genes control reproductive system development in Caenorhabditis elegans. (ncsu.edu)
  • The new zinc finger peptides of the invention may be particularly useful in the modulation of target genes associated with expanded GGGGCC hexanucleotide repeats or CGG trinucleotide repeats, and more specifically the targeted repression of such genes. (imperial.tech)
  • Likewise, hypoxic breast cancer cells showed higher propensity to increase expression of oncogenes and to decrease expression of tumor suppressor genes ( Jefford and Irminger-Finger, 2006 ). (frontiersin.org)
  • A transcriptional activator and oncogene protein that contains two CYS2-HIS2 ZINC FINGERS . (nih.gov)
  • A DNA-binding protein that contains an N-terminal BTB (POZ) DOMAIN and C-terminal CYS2-HIS2 ZINC FINGERS . (nih.gov)
  • Furthermore, 8 of 9 mothers of children with CHB had antibody reactivity against amino acids 1-135 of the Ro 52-kd protein, containing 2 putative zinc fingers reconstituted under reducing conditions. (nih.gov)
  • Interoperable with Gal4, the new system's key component is a fusion protein in which the DNA-binding domain of Gal4 has been replaced with a zinc finger domain with a different DNA-binding specificity. (a-star.edu.sg)
  • The human zinc finger antiviral protein (ZAP) is capable of inhibiting several major human pathogens, including Influenza A virus and SARS-CoV-2. (europa.eu)
  • SARS-CoV-2 Is Restricted by Zinc Finger Antiviral Protein despite Preadaptation to the Low-CpG Environment in Humans. (cdc.gov)
  • The zinc finger amino acid sequences of the KRC ZAS domains are compared. (biomedcentral.com)
  • The critical amino acid residues within the α helical regions of the zinc finger regions are identical at all corresponding positions between the first and second zinc fingers of the ZAS-N and ZAS-C domains except at position 3 of the first zinc finger (outlined in gray) and at position 2 of the second zinc finger (outlined in gray). (biomedcentral.com)
  • Zn fingers 5-10 are required for maximal binding of ZFP100 to a 20-amino-acid region of Lsm11, a U7 snRNP core protein. (utmb.edu)
  • Their binding properties depend on the amino acid sequence of the finger domains and of the linker between fingers, as well as on the higher-order structures and the number of fingers. (embl.de)
  • C2H2-type (classical) zinc fingers (Znf) were the first class to be characterised. (embl.de)
  • They contain a short beta hairpin and an alpha helix (beta/beta/alpha structure), where a single zinc atom is held in place by Cys(2)His(2) (C2H2) residues in a tetrahedral array. (embl.de)
  • This entry represents the classical C2H2 zinc finger domain. (embl.de)
  • AoSAP8-P encoding A20 and/or AN1 type zinc finger protein in asparagus officinalis L. Improving stress tolerance in transgenic Nicotiana sylvestris. (bvsalud.org)
  • The full length CDS of an A20 and AN1 type zinc finger gene (named AoSAP8-P), located nearby the male specific Y chromosome (MSY) region of Asparagus officinalis ( garden asparagus) was amplified by RT-PCR from purple passion. (bvsalud.org)
  • Classic zinc finger domains (cZFs) consist of a beta-hairpin followed by an alpha-helix. (rcsb.org)
  • They are similar structurally to RING FINGER DOMAINS, with a globular fold topology of two BETA-SHEETS and an ALPHA-HELIX. (jefferson.edu)
  • Comparison of KRC protein zinc finger domains. (biomedcentral.com)
  • The zinc finger 1 and zinc finger 2 domains within the ZAS domains are designated in green and blue font, respectively, in the consensus sequence. (biomedcentral.com)
  • Comparisons with other mammalian ZFP100 orthologs show that the central Zn fingers sufficient for in vivo activity are most highly conserved, whereas the number and sequence of the Zn fingers in the N- and C-terminal domains vary. (utmb.edu)
  • We generated two synthetic zinc-finger DNA-binding domains (ZF-DBDs) targeting this sequence. (elsevier.com)
  • Znf domains are often found in clusters, where fingers can have different binding specificities. (embl.de)
  • To obtain structural information, we synthesized single and double zinc finger peptides from the yeast transcription activator ADR1, and assessed the metal-binding and DNA-binding properties of these peptides, as well as the solution structure of the metal-stabilized domains, with the use of a variety of spectroscopic techniques. (embl.de)
  • Mutations conferring drug resistance were not confined to the N-terminal p53/Nutlin-binding domain, and were additionally seen in the acidic, zinc finger and RING domains. (ntu.edu.sg)
  • 1985. Effects of marginal zinc deficiency on subclinical lead toxicity in the rat neonate. (cdc.gov)
  • Modulation of tissue trace metal concentrations in weanling rats fed different levels of zinc and exposed to oral lead and cadmium. (cdc.gov)
  • The present invention provides new zinc finger peptides and encoding nucleic acid molecules that can be used for the modulation of gene expression in vitro and/or in vivo. (imperial.tech)
  • Our prototype links the tandem zinc finger (TZF) domain from tristetraprolin (TTP) to the endoribonuclease RNase4 (R4). (cancer.gov)
  • We, recently, reported the Arabidopsis thaliana Tandem Zinc Finger protein 9 (TZF9) to be an RNA-binding protein co-localizing with components of RNA granules. (uni-halle.de)
  • We have studied the transcriptional co-regulator Friend of GATA (FOG), which contains nine zinc fingers. (rcsb.org)
  • Sangamo BioSciences, a Richmond, California-based pharmaceutical company, has developed a 'zinc fingers' technology that can home in on the CCR5 section of cellular DNA and artificially create a functional equivalent of the delta-32 mutation. (scientificamerican.com)
  • Of the 18 zinc fingers contained within ZFP100, the region encompassing fingers 2-6 is sufficient to maintain CB localization. (utmb.edu)
  • Encodes a zinc finger protein involved in high light and cold acclimation. (or.jp)
  • Kong W , Liu X , Yin G , Zheng S , Zhu A , Yu P , Shan Y , Ying R , Zhang J , . Extracellular vesicle derived miR-544 downregulates expression of tumor suppressor promyelocytic leukemia zinc finger resulting in increased peritoneal metastasis in gastric cancer. (aging-us.com)
  • Our results demonstrate that expression of the tumor suppressor promyelocytic leukemia zinc finger (PLZF) is decreased in GC tissues and PM lesions from GC patients. (aging-us.com)
  • The binding sites of Zinc atom in the Solution Structure of Miz-1 Zinc Finger 7 (pdb code 2m0f ). (atomistry.com)
  • This binding sites where shown within 5.0 Angstroms radius around Zinc atom. (atomistry.com)
  • In the classic zinc finger, one zinc atom is bound to two cysteines and two histidines. (bvsalud.org)
  • The Implications of Zinc Therapy in Combating the COVID-19 Global Pandemic. (cdc.gov)
  • A competitive ELISA for quantitative measurement of Human PR domain zinc finger protein 1 (PRDM1) in samples from blood, plasma, serum, cell culture supernatant and other biological fluids. (blimp-1.com)
  • To understand the molecular consequences of dysregulated RNA regulons in cancer, the goal of this exploratory, high-risk/high-reward R21 proposal is to develop a zinc finger-directed RNA-cleaving agent to suppress RNA regulons that are upregulated in many tumors. (cancer.gov)
  • Antagonistic effects of zinc and aluminum on lead inhibition of *-aminolevulinic acid dehydratase. (cdc.gov)
  • 1994. Inhibition of Na+-glucose cotransport in kidney cortical cells by cadmium and copper: Protection by zinc. (cdc.gov)
  • 1976. The in vitro effect of zinc on the inhibition of human *-aminolevulinic acid dehydratase by lead. (cdc.gov)
  • PHD Zinc Fingers" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus, MeSH (Medical Subject Headings) . (jefferson.edu)
  • Zinc oxide in Portland cement. (elsevier.com)
  • In general, workers were concerned about their workplace exposures, specifically to acids and zinc oxide dust. (cdc.gov)
  • Engineered zinc finger protein transcription factors (ZFP TFs) can be designed to specifically increase the level of a therapeutically important protein from its native gene in a patients' own cells. (michaeljfox.org)
  • The protein contains a zinc finger and a polyalanine tract similar to ones previously implicated in DNA binding and transactivation or repression, respectively. (elsevier.com)
  • This is the protein part of a two-part zinc finger mold, where the DNA model binds into the Zn Model. (nih.gov)
  • To do this they targeted zinc finger- Fok I fusions to a sequence within the extremely well conserved long terminal repeat (LTR) U3 region of the HIV-1 provirus. (epigenie.com)
  • Establishment of transgenic mice carrying gene encoding human zinc finger protein 191. (wikigenes.org)
  • 1988. Antagonistic effect of zinc in lead treated developing chick embryos. (cdc.gov)