Nonprocessive methylation by Dot1 leads to functional redundancy of histone H3K79 methylation states.
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Antigenic variation in Trypanosoma brucei: joining the DOTsIdentification of arginine- and lysine-methylation in the proteome of Saccharomyces cerevisiae and its functional implicationsDevelopmental roles of the histone lysine demethylasesSynthesis of lysine methyltransferase inhibitorsChemical probes of histone lysine methyltransferasesDot1-dependent histone H3K79 methylation promotes activation of the Mek1 meiotic checkpoint effector kinase by regulating the Hop1 adaptorStructural basis for the role of the Sir3 AAA+ domain in silencing: interaction with Sir4 and unmethylated histone H3K79Nonprocessive [2 + 2]e- off-loading reductase domains from mycobacterial nonribosomal peptide synthetasesConformational adaptation drives potent, selective and durable inhibition of the human protein methyltransferase DOT1LMultiple histone modifications in euchromatin promote heterochromatin formation by redundant mechanisms in Saccharomyces cerevisiae.Spt10 and Spt21 are required for transcriptional silencing in Saccharomyces cerevisiae.Histone methylation modifiers in cellular signaling pathwaysMethylation of histone H3 on lysine 79 associates with a group of replication origins and helps limit DNA replication once per cell cycleThe role of multiple marks in epigenetic silencing and the emergence of a stable bivalent chromatin stateDirect screening for chromatin status on DNA barcodes in yeast delineates the regulome of H3K79 methylation by Dot1Degree of recruitment of DOT1L to MLL-AF9 defines level of H3K79 Di- and tri-methylation on target genes and transformation potential.Quantitative proteomic analysis of histone modificationsCREB trans-activation of disruptor of telomeric silencing-1 mediates forskolin inhibition of CTGF transcription in mesangial cells.NRMT2 is an N-terminal monomethylase that primes for its homologue NRMT1.Patterns and mechanisms of ancestral histone protein inheritance in budding yeast.A medicinal chemistry perspective for targeting histone H3 lysine-79 methyltransferase DOT1L.Histone H2B C-terminal helix mediates trans-histone H3K4 methylation independent of H2B ubiquitination.Quantitative proteomic discovery of dynamic epigenome changes that control human cytomegalovirus (HCMV) infectionSymmetry, asymmetry, and kinetics of silencing establishment in Saccharomyces cerevisiae revealed by single-cell optical assaysAnalysis of the tolerance to DNA alkylating damage in MEC1 and RAD53 checkpoint mutants of Saccharomyces cerevisiae.Selective inhibitors of protein methyltransferasesA dual role of H4K16 acetylation in the establishment of yeast silent chromatin.Breaking an epigenetic chromatin switch: curious features of hysteresis in Saccharomyces cerevisiae telomeric silencing.Linking cell cycle to histone modifications: SBF and H2B monoubiquitination machinery and cell-cycle regulation of H3K79 dimethylation.Dot1 histone methyltransferases share a distributive mechanism but have highly diverged catalytic properties.Mechanism for epigenetic variegation of gene expression at yeast telomeric heterochromatinH3K79me3T80ph is a Novel Histone Dual Modification and a Mitotic Indicator in Melanoma.A prototypic lysine methyltransferase 4 from archaea with degenerate sequence specificity methylates chromatin proteins Sul7d and Cren7 in different patterns.Controlling histone methylation via trans-histone pathways.Sirtuin 1 functionally and physically interacts with disruptor of telomeric silencing-1 to regulate alpha-ENaC transcription in collecting duct.A lesson learned from the H3.3K27M mutation found in pediatric glioma: a new approach to the study of the function of histone modifications in vivo?Structure-activity analysis of semisynthetic nucleosomes: mechanistic insights into the stimulation of Dot1L by ubiquitylated histone H2B.Two Dot1 isoforms in Saccharomyces cerevisiae as a result of leaky scanning by the ribosome.Sex-specific chromatin landscapes in an ultra-compact chordate genome.Dynamics of DOT1L localization and H3K79 methylation during meiotic prophase I in mouse spermatocytes.
P2860
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P2860
Nonprocessive methylation by Dot1 leads to functional redundancy of histone H3K79 methylation states.
description
2008 nî lūn-bûn
@nan
2008年の論文
@ja
2008年学术文章
@wuu
2008年学术文章
@zh
2008年学术文章
@zh-cn
2008年学术文章
@zh-hans
2008年学术文章
@zh-my
2008年学术文章
@zh-sg
2008年學術文章
@yue
2008年學術文章
@zh-hant
name
Nonprocessive methylation by D ...... tone H3K79 methylation states.
@en
Nonprocessive methylation by D ...... tone H3K79 methylation states.
@nl
type
label
Nonprocessive methylation by D ...... tone H3K79 methylation states.
@en
Nonprocessive methylation by D ...... tone H3K79 methylation states.
@nl
prefLabel
Nonprocessive methylation by D ...... tone H3K79 methylation states.
@en
Nonprocessive methylation by D ...... tone H3K79 methylation states.
@nl
P2093
P2860
P356
P1476
Nonprocessive methylation by D ...... tone H3K79 methylation states.
@en
P2093
Floor Frederiks
Gideon Oudgenoeg
Maarten Fornerod
Manuel Tzouros
Tibor van Welsem
P2860
P2888
P304
P356
10.1038/NSMB.1432
P577
2008-05-30T00:00:00Z
P5875
P6179
1026808095