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35 Cards in this Set
- Front
- Back
activation domain
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a part of a transcription factor required for the activation of target-gene transcription; it may bind to components of the transcriptional machinery or may recruit proteins that modify chromatin structure or both
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Barr body
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a densely staining mass that represents an inactivated X chromasome
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barrier insulator
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a DNA element that prevents the spread of heterochromatin by serving as a binding site for proteins that maintain euchromatic chromatin modifications such as histone acetylation
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chromatin remodeling
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changes in nucleosome position along DNA
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coactivator
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a special class of eukaryotic regulatory complex that serves as a bridge to bring together regulatory proteins and RNA polymerase II
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constitutive heterochromatin
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chromosomal regions of permanently condensed chromatin usually around the telomeres and centromeres
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corepressor
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a protein or protein complex that acts in concert with a repressor protein to repress transcription, often by modifying chromatin structure; usually not a DNA-binding entity itself
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dosage compensation
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the process in organisms using a chromosomal sex-determination mechanism (such as XX vs XY) that allows standard structural genes on the sex chromosomes to be expressed at the same levels in females and in males, regardless of the number of sex chromosomes. in mammals, dosage compensation operates by maintaining only a single active X chromosome in each cell; in Drosophila, it operates by hyperactivating the male X chromosome
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enhanceosome
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the macromolecular assembly responsible for interaction between enhancer elements and the promoter regions of genes
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enhancer (element/mutation)
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element: a cis-acting regulatory sequence that can elevate levels of transcription from an adjacent promoter. many tissue specific enhancers can determine spatial patterns of gene expression in higher eukaryotes. enhancers can act on promoters over many tens of kilobases of DNA and can be 5' or 3' of the promoters that they regulate
mutation: a modifier mutation that makes the phenotype of mutation of another gene more severe |
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enhancer-blocking insulator
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regulatory elements postioned between a promoter and an enhancer. their presence prevents the promoter from being activated by the enhancer
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epigenetic inheritance
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heritable modifications in gene function not due to changes in the base sequence of the DNA of the organism, examples are paramutation, x-chromosome inactivation, and parental imprinting
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epigenetic mark
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a heritable alteration, such as DNA methylation or a histone modification, that leaves the DNA sequence unchanged
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epigenetic silencing
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the reversable alteration of a gene due to chromatin structure
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euchromatin
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a less-condensed chromosomal region, thought to contain most of the normally functioning genes
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gene silencing
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a gene that is not expressed owing to epigenetic regulation. unlike genes that are mutant due to DNA sequence alterations, genes inactivated by silencing can be reactivated
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genomic imprinting
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a phenomenon in which a gene inherited form one of the parents is not expressed, even though both gene copies are functional.imprinted genes are methylated and inactivated in the formation of male or female gametes
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hemimethylation
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where one DNA sequence where one strand is methylated and other one isn't
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heterochromatin
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densely staining condensed chromosomal regions, believed to be for the most part genetically inert
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herterochromatin protein-1
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a protein necessary for the maintenance of heterochromatin
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histone code
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refers to the pattern of modification (eg acetylation, methylation, phosphorylation) of the histone tails that may carry information required for correct chromatin assembly
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histone deacetylase (HDAT)
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the enxymatic activity that removes an acetyle group from a histone tail, which promotes the pression of gene transcription
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histone tail
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the end of a histone protein protruding from the core nucleosome and subjected to posttranslational modification
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hyperacetylation
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an overabundance of acetyl groups attached to certain amino acids of the histone tails. transcriptionally active chromatin is usually hyperacetylated
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hypoacetylation
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an underabundance of acetyle groups on certain amino acids of the histone tails. transcriptionally inactive chromatin is usually hypoacetylated
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maternal imprinting
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the expression of a gene only when inherited from the father, because the copy of the gene inherited from the mother is inactive due to methylation in th ecourse of gamete formation
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mediator complex
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a protein complex that acts as an adaptor that interacts with transcription factors bound to regulatory sites and with general initiation factors and RNA polymerase II-mediated transcription
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monoallelic inheritance
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inheriting one allele?
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paternal imprinting
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the expression of a gene only when inherited form the mother, because the allele of the ene inherited from the father is inactive due to methylation in the course of gamete formation
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pheromone
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a molecule that promotes mating behavior
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position-effect variegation (PEV)
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variegation causeecd byt the inactivation of a gene in some cells through its abnormal juxtaposition with heterochromatin
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promoter-proximal element
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the series of transcription-factor binding sites located near the core promoter
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reporter gene
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a gene whose phenotypic expression is easy to monitor; used to study tissue-specific promoter and enhancer activities in transgenes
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synergistic effect
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a feature of eukaryoti regulatory proteins for which the transciptional activation mediated by the interaction of several proteins is greater than the sum of the effects of the proteins taken individually
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upstream activation sequence (UAS)
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a DNA sequence of yeast located 5' of the gene promoter; a transcription factor binds to the UAS to positively regulate gene expresion
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