The highly conserved N-terminal domains of histones H3 and H4 are required for normal cell cycle progression
about
SirT2 is a histone deacetylase with preference for histone H4 Lys 16 during mitosisHuman CENP-A contains a histone H3 related histone fold domain that is required for targeting to the centromereHistone H3 specific acetyltransferases are essential for cell cycle progression.Histones H3 and H4 are components of upstream activation factor required for the high-level transcription of yeast rDNA by RNA polymerase IRoles of transcription factor Mot3 and chromatin in repression of the hypoxic gene ANB1 in yeastSth1p, a Saccharomyces cerevisiae Snf2p/Swi2p homolog, is an essential ATPase in RSC and differs from Snf/Swi in its interactions with histones and chromatin-associated proteins.Suppressor analysis of a histone defect identifies a new function for the hda1 complex in chromosome segregation.Histones are required for transcription of yeast rRNA genes by RNA polymerase I.Histone H3 lysine 4 methylation is mediated by Set1 and required for cell growth and rDNA silencing in Saccharomyces cerevisiae.Redundant roles for histone H3 N-terminal lysine residues in subtelomeric gene repression in Saccharomyces cerevisiaeAmino termini of histones H3 and H4 are required for a1-alpha2 repression in yeast.Histone-histone interactions and centromere function.Histone chaperones link histone nuclear import and chromatin assemblyMutagenesis of pairwise combinations of histone amino-terminal tails reveals functional redundancy in budding yeast.Mutational analysis of H3 and H4 N termini reveals distinct roles in nuclear import.Global and specific transcriptional repression by the histone H3 amino terminus in yeastA novel histone H4 mutant defective in nuclear division and mitotic chromosome transmission.In silico functional characterization of a double histone fold domain from the Heliothis zea virus 1.Histone h3 exerts a key function in mitotic checkpoint control.Histone H3 N-terminal mutations allow hyperactivation of the yeast GAL1 gene in vivo.Progression into the first meiotic division is sensitive to histone H2A-H2B dimer concentration in Saccharomyces cerevisiaeRole of histone acetylation in the assembly and modulation of chromatin structures.The SIN3/RPD3 deacetylase complex is essential for G(2) phase cell cycle progression and regulation of SMRTER corepressor levels.H4 replication-dependent diacetylation and Hat1 promote S-phase chromatin assembly in vivoSubnucleosomal structures and nucleosome asymmetry across a genomeOrchestration of chromatin-based processes: mind the TRRAP.Conservation of deposition-related acetylation sites in newly synthesized histones H3 and H4.Activator-independent transcription of Snf1-dependent genes in mutants lacking histone tailsDifferential contributions of histone H3 and H4 residues to heterochromatin structure.Loss of Sin3/Rpd3 histone deacetylase restores the DNA damage response in checkpoint-deficient strains of Saccharomyces cerevisiae.Chromatin-modifiying enzymes are essential when the Saccharomyces cerevisiae morphogenesis checkpoint is constitutively activated.Chromatin assembly factor I contributes to the maintenance, but not the re-establishment, of silencing at the yeast silent mating loci.The amino-terminal tails of histones H2A and H3 coordinate efficient base excision repair, DNA damage signaling and postreplication repair in Saccharomyces cerevisiaeGenome-wide location and regulated recruitment of the RSC nucleosome-remodeling complex.RSC regulates nucleosome positioning at Pol II genes and density at Pol III genesDeposition-related sites K5/K12 in histone H4 are not required for nucleosome deposition in yeastEfficient transcriptional silencing in Saccharomyces cerevisiae requires a heterochromatin histone acetylation patternHistone cleavage as a mechanism for epigenetic regulation: current insights and perspectives.Cryptosporidium parvum mitochondrial-type HSP70 targets homologous and heterologous mitochondria.Set2-dependent K36 methylation is regulated by novel intratail interactions within H3
P2860
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P2860
The highly conserved N-terminal domains of histones H3 and H4 are required for normal cell cycle progression
description
1991 nî lūn-bûn
@nan
1991 թուականի Օգոստոսին հրատարակուած գիտական յօդուած
@hyw
1991 թվականի օգոստոսին հրատարակված գիտական հոդված
@hy
1991年の論文
@ja
1991年論文
@yue
1991年論文
@zh-hant
1991年論文
@zh-hk
1991年論文
@zh-mo
1991年論文
@zh-tw
1991年论文
@wuu
name
The highly conserved N-termina ...... normal cell cycle progression
@ast
The highly conserved N-termina ...... normal cell cycle progression
@en
type
label
The highly conserved N-termina ...... normal cell cycle progression
@ast
The highly conserved N-termina ...... normal cell cycle progression
@en
prefLabel
The highly conserved N-termina ...... normal cell cycle progression
@ast
The highly conserved N-termina ...... normal cell cycle progression
@en
P2093
P2860
P356
P1476
The highly conserved N-termina ...... normal cell cycle progression
@en
P2093
B A Mittman
B A Morgan
P2860
P304
P356
10.1128/MCB.11.8.4111
P407
P577
1991-08-01T00:00:00Z