Histone H3 N-terminal mutations allow hyperactivation of the yeast GAL1 gene in vivo.
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Human CENP-A contains a histone H3 related histone fold domain that is required for targeting to the centromereHistone sumoylation is a negative regulator in Saccharomyces cerevisiae and shows dynamic interplay with positive-acting histone modificationsMitogen-stimulated phosphorylation of histone H3 is targeted to a small hyperacetylation-sensitive fractionHistone acetyltransferase activity is conserved between yeast and human GCN5 and is required for complementation of growth and transcriptional activationAssembly of CENP-A into centromeric chromatin requires a cooperative array of nucleosomal DNA contact sitesMethods designed for the identification and characterization ofin vitro andin vivo chromatin assembly mutants inSaccharomyces cerevisiaeThe conformational flexibility of the C-terminus of histone H4 promotes histone octamer and nucleosome stability and yeast viabilityRNA polymerase II and III transcription factors can stimulate DNA replication by modifying origin chromatin structures.Novel role for checkpoint Rad53 protein kinase in the initiation of chromosomal DNA replication in Saccharomyces cerevisiae.BUR1 and BUR2 encode a divergent cyclin-dependent kinase-cyclin complex important for transcription in vivo.The N terminus of the centromere H3-like protein Cse4p performs an essential function distinct from that of the histone fold domain.Direct role for the Rpd3 complex in transcriptional induction of the anaerobic DAN/TIR genes in yeastType B histone acetyltransferase Hat1p participates in telomeric silencingCks1, Cdk1, and the 19S proteasome collaborate to regulate gene induction-dependent nucleosome eviction in yeastHistones are required for transcription of yeast rRNA genes by RNA polymerase I.Redundant roles for histone H3 N-terminal lysine residues in subtelomeric gene repression in Saccharomyces cerevisiaeHistone octamer function in vivo: mutations in the dimer-tetramer interfaces disrupt both gene activation and repressionGlobal and specific transcriptional repression by the histone H3 amino terminus in yeastA novel histone H4 mutant defective in nuclear division and mitotic chromosome transmission.H3 k36 methylation helps determine the timing of cdc45 association with replication originsHir proteins are required for position-dependent gene silencing in Saccharomyces cerevisiae in the absence of chromatin assembly factor IAlterations in DNA replication and histone levels promote histone gene amplification in Saccharomyces cerevisiae.Analysis of primary structural determinants that distinguish the centromere-specific function of histone variant Cse4p from histone H3.Histone acetylation at promoters is differentially affected by specific activators and repressors.Role of histone acetylation in the assembly and modulation of chromatin structures.Yeast histone H3 and H4 N termini function through different GAL1 regulatory elements to repress and activate transcriptionThe role of histone acetylation in memory formation and cognitive impairments.Analysis of histone acetyltransferase and histone deacetylase families of Arabidopsis thaliana suggests functional diversification of chromatin modification among multicellular eukaryotes.Localized histone acetylation and deacetylation triggered by the homologous recombination pathway of double-strand DNA repair.Simultaneous mutation of methylated lysine residues in histone H3 causes enhanced gene silencing, cell cycle defects, and cell lethality in Saccharomyces cerevisiae.Histone modification governs the cell cycle regulation of a replication-independent chromatin assembly pathway in Saccharomyces cerevisiaeEarly disruption of centromeric chromatin organization in centromere protein A (Cenpa) null mice.Differential contributions of histone H3 and H4 residues to heterochromatin structure.PRB1 is required for clipping of the histone H3 N terminal tail in Saccharomyces cerevisiae.Uncoupling histone turnover from transcription-associated histone H3 modifications.Acetylation of histone H4 plays a primary role in enhancing transcription factor binding to nucleosomal DNA in vitro.All four core histone N-termini contain sequences required for the repression of basal transcription in yeastEverything you ever wanted to know about Saccharomyces cerevisiae telomeres: beginning to end.Deposition-related sites K5/K12 in histone H4 are not required for nucleosome deposition in yeastA new class of histone H2A mutations in Saccharomyces cerevisiae causes specific transcriptional defects in vivo
P2860
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P2860
Histone H3 N-terminal mutations allow hyperactivation of the yeast GAL1 gene in vivo.
description
1992 nî lūn-bûn
@nan
1992 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
1992 թվականի սեպտեմբերին հրատարակված գիտական հոդված
@hy
1992年の論文
@ja
1992年論文
@yue
1992年論文
@zh-hant
1992年論文
@zh-hk
1992年論文
@zh-mo
1992年論文
@zh-tw
1992年论文
@wuu
name
Histone H3 N-terminal mutations allow hyperactivation of the yeast GAL1 gene in vivo.
@ast
Histone H3 N-terminal mutations allow hyperactivation of the yeast GAL1 gene in vivo.
@en
type
label
Histone H3 N-terminal mutations allow hyperactivation of the yeast GAL1 gene in vivo.
@ast
Histone H3 N-terminal mutations allow hyperactivation of the yeast GAL1 gene in vivo.
@en
prefLabel
Histone H3 N-terminal mutations allow hyperactivation of the yeast GAL1 gene in vivo.
@ast
Histone H3 N-terminal mutations allow hyperactivation of the yeast GAL1 gene in vivo.
@en
P2860
P1433
P1476
Histone H3 N-terminal mutations allow hyperactivation of the yeast GAL1 gene in vivo
@en
P2093
P2860
P304
P356
10.1002/J.1460-2075.1992.TB05408.X
P407
P577
1992-09-01T00:00:00Z