Histone variant H2A.Z marks the 5' ends of both active and inactive genes in euchromatin
about
The insulator binding protein CTCF positions 20 nucleosomes around its binding sites across the human genomeUncoupling transcription from covalent histone modification.Essential role of p18Hamlet/SRCAP-mediated histone H2A.Z chromatin incorporation in muscle differentiationH3.3/H2A.Z double variant-containing nucleosomes mark 'nucleosome-free regions' of active promoters and other regulatory regionsANP32E is a histone chaperone that removes H2A.Z from chromatinThe euchromatic and heterochromatic landscapes are shaped by antagonizing effects of transcription on H2A.Z depositionHistone sumoylation is a negative regulator in Saccharomyces cerevisiae and shows dynamic interplay with positive-acting histone modificationsProximity of H2A.Z containing nucleosome to the transcription start site influences gene expression levels in the mammalian liver and brainAnalysis of human histone H2AZ deposition in vivo argues against its direct role in epigenetic templating mechanismsOpposing roles for Set2 and yFACT in regulating TBP binding at promotersThe interplay of histone modifications - writers that readChromatin Dynamics in Vivo: A Game of Musical ChairsPost-translational modifications of histones that influence nucleosome dynamicsGenetic and epigenetic influence on the response to environmental particulate matterExpression of P. falciparum var genes involves exchange of the histone variant H2A.Z at the promoterRegulation of DCC localization by HTZ-1/H2A.Z and DPY-30 does not correlate with H3K4 methylation levelsRestricting dosage compensation complex binding to the X chromosomes by H2A.Z/HTZ-1ING4 Mediates Crosstalk between Histone H3 K4 Trimethylation and H3 Acetylation to Attenuate Cellular TransformationAnp32e, a higher eukaryotic histone chaperone directs preferential recognition for H2A.ZMolecular basis and specificity of H2A.Z-H2B recognition and deposition by the histone chaperone YL1N terminus of Swr1 binds to histone H2AZ and provides a platform for subunit assembly in the chromatin remodeling complexGlobal regulation of H2A.Z localization by the INO80 chromatin-remodeling enzyme is essential for genome integrityThe Isw2 chromatin-remodeling ATPase cooperates with the Fkh2 transcription factor to repress transcription of the B-type cyclin gene CLB2NuA4-directed chromatin transactions throughout the Saccharomyces cerevisiae genome.Eaf1 is the platform for NuA4 molecular assembly that evolutionarily links chromatin acetylation to ATP-dependent exchange of histone H2A variants.Molecular architecture of the ATP-dependent chromatin-remodeling complex SWR1.DNA polymerase epsilon, acetylases and remodellers cooperate to form a specialized chromatin structure at a tRNA insulator.Coordinate control of gene expression noise and interchromosomal interactions in a MAP kinase pathwayThe ATP-dependent chromatin remodeling enzyme Fun30 represses transcription by sliding promoter-proximal nucleosomes.Interaction of transcriptional regulators with specific nucleosomes across the Saccharomyces genome.Histone variant Htz1 promotes histone H3 acetylation to enhance nucleotide excision repair in Htz1 nucleosomes.SWI/SNF-like chromatin remodeling factor Fun30 supports point centromere function in S. cerevisiae.Distinct roles for SWR1 and INO80 chromatin remodeling complexes at chromosomal double-strand breaks.The RSC chromatin remodelling enzyme has a unique role in directing the accurate positioning of nucleosomesRegulation of rRNA synthesis by TATA-binding protein-associated factor Mot1.The Tup1 corepressor directs Htz1 deposition at a specific promoter nucleosome marking the GAL1 gene for rapid activation.NuA4-dependent acetylation of nucleosomal histones H4 and H2A directly stimulates incorporation of H2A.Z by the SWR1 complex.Interaction of a DNA zip code with the nuclear pore complex promotes H2A.Z incorporation and INO1 transcriptional memoryDNA looping facilitates targeting of a chromatin remodeling enzyme.Histone variant H2A.Z and RNA polymerase II transcription elongation.
P2860
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P2860
Histone variant H2A.Z marks the 5' ends of both active and inactive genes in euchromatin
description
2005 nî lūn-bûn
@nan
2005 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2005 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
2005年の論文
@ja
2005年論文
@yue
2005年論文
@zh-hant
2005年論文
@zh-hk
2005年論文
@zh-mo
2005年論文
@zh-tw
2005年论文
@wuu
name
Histone variant H2A.Z marks the 5' ends of both active and inactive genes in euchromatin
@ast
Histone variant H2A.Z marks the 5' ends of both active and inactive genes in euchromatin
@en
Histone variant H2A.Z marks the 5' ends of both active and inactive genes in euchromatin.
@nl
type
label
Histone variant H2A.Z marks the 5' ends of both active and inactive genes in euchromatin
@ast
Histone variant H2A.Z marks the 5' ends of both active and inactive genes in euchromatin
@en
Histone variant H2A.Z marks the 5' ends of both active and inactive genes in euchromatin.
@nl
prefLabel
Histone variant H2A.Z marks the 5' ends of both active and inactive genes in euchromatin
@ast
Histone variant H2A.Z marks the 5' ends of both active and inactive genes in euchromatin
@en
Histone variant H2A.Z marks the 5' ends of both active and inactive genes in euchromatin.
@nl
P2093
P2860
P3181
P1433
P1476
Histone variant H2A.Z marks the 5' ends of both active and inactive genes in euchromatin
@en
P2093
Chih Long Liu
Marc D Meneghini
Marie Z Bao
Paul D Hartley
Ryan M Raisner
Stuart L Schreiber
P2860
P304
P3181
P356
10.1016/J.CELL.2005.10.002
P407
P577
2005-10-21T00:00:00Z