Cotranscriptional histone H2B monoubiquitylation is tightly coupled with RNA polymerase II elongation rate

被引:73
作者
Fuchs, Gilad [1 ]
Hollander, Dror [2 ]
Voichek, Yoav [3 ]
Ast, Gil [2 ]
Oren, Moshe [1 ]
机构
[1] Weizmann Inst Sci, Dept Mol & Cell Biol, IL-76100 Rehovot, Israel
[2] Tel Aviv Univ, Sackler Fac Med, Dept Human Mol Genet & Biochem, IL-69978 Tel Aviv, Israel
[3] Weizmann Inst Sci, Dept Mol Genet, IL-76100 Rehovot, Israel
基金
欧洲研究理事会; 以色列科学基金会;
关键词
EXON-INTRON STRUCTURE; E3 UBIQUITIN LIGASE; HUMAN GENOME; H3; METHYLATION; HUMAN-CELLS; STEM-CELLS; EPIGENETIC MODIFICATIONS; CHROMATIN MODIFICATIONS; REGULATORY PATHWAY; TUMOR-SUPPRESSOR;
D O I
10.1101/gr.176487.114
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Various histone modifications decorate nucleosomes within transcribed genes. Among these, monoubiquitylation of histone H2B (H2Bubl) and methylation of histone H3 on lysines 36 (H3K36me2/3) and 79 (H3K79me2/3) correlate positively with gene expression. By measuring the progression of the transcriptional machinery along genes within live cells, we now report that H2B monoubiquitylation occurs cotranscriptionally and accurately reflects the advance of RNA polymerase II (Pol II). In contrast, H3K36me3 and H3K79me2 are less dynamic and represent Pol II movement less faithfully. High-resolution ChIP-seq reveals that H2Bubl levels are selectively reduced at exons and decrease in an exon-dependent stepwise manner toward the 3' end of genes. Exonic depletion of H2Bubl in gene bodies is highly correlated with Pol II pausing at exons, suggesting elongation rate changes associated with intron-exon structure. In support of this notion, H2Bubl levels were found to be significantly correlated with transcription elongation rates measured in various cell lines. Overall, our data shed light on the organization of H2Bubl within transcribed genes and single out H2Bubl as a reliable marker for ongoing transcription elongation.
引用
收藏
页码:1572 / 1583
页数:12
相关论文
共 95 条
[1]   A module of negative feedback regulators defines growth factor signaling [J].
Amit, Ido ;
Citri, Ami ;
Shay, Tal ;
Lu, Yiling ;
Katz, Menachem ;
Zhang, Fan ;
Tarcic, Gabi ;
Siwak, Doris ;
Lahad, John ;
Jacob-Hirsch, Jasmine ;
Amariglio, Ninette ;
Vaisman, Nora ;
Segal, Eran ;
Rechavi, Gideon ;
Alon, Uri ;
Mills, Gordon B. ;
Domany, Eytan ;
Yarden, Yosef .
NATURE GENETICS, 2007, 39 (04) :503-512
[2]  
[Anonymous], 2014, The R Foundation for Statistical Computing
[3]   High-resolution profiling of histone methylations in the human genome [J].
Barski, Artern ;
Cuddapah, Suresh ;
Cui, Kairong ;
Roh, Tae-Young ;
Schones, Dustin E. ;
Wang, Zhibin ;
Wei, Gang ;
Chepelev, Iouri ;
Zhao, Keji .
CELL, 2007, 129 (04) :823-837
[4]   Genome-wide function of H2B ubiquitylation in promoter and genic regions [J].
Batta, Kiran ;
Zhang, Zhenhai ;
Yen, Kuangyu ;
Goffman, David B. ;
Pugh, B. Franklin .
GENES & DEVELOPMENT, 2011, 25 (21) :2254-2265
[5]   The complex language of chromatin regulation during transcription [J].
Berger, Shelley L. .
NATURE, 2007, 447 (7143) :407-412
[6]   Characterization of the Contradictory Chromatin Signatures at the 3′ Exons of Zinc Finger Genes [J].
Blahnik, Kimberly R. ;
Dou, Lei ;
Echipare, Lorigail ;
Iyengar, Sushma ;
O'Geen, Henriette ;
Sanchez, Erica ;
Zhao, Yongjun ;
Marra, Marco A. ;
Hirst, Martin ;
Costello, Joseph F. ;
Korf, Ian ;
Farnham, Peggy J. .
PLOS ONE, 2011, 6 (02)
[7]   A tumor suppressor function of Smurf2 associated with controlling chromatin landscape and genome stability through RNF20 [J].
Blank, Michael ;
Tang, Yi ;
Yamashita, Motozo ;
Burkett, Sandra S. ;
Cheng, Steven Y. ;
Zhang, Ying E. .
NATURE MEDICINE, 2012, 18 (02) :227-234
[8]   Dynamic Integration of Splicing within Gene Regulatory Pathways [J].
Braunschweig, Ulrich ;
Gueroussov, Serge ;
Plocik, Alex M. ;
Graveley, Brenton R. ;
Blencowe, Benjamin J. .
CELL, 2013, 152 (06) :1252-1269
[9]   Gene silencing -: Trans-histone regulatory pathway in chromatin [J].
Briggs, SD ;
Xiao, TJ ;
Sun, ZW ;
Caldwell, JA ;
Shabanowitz, J ;
Hunt, DF ;
Allis, CD ;
Strahl, BD .
NATURE, 2002, 418 (6897) :498-498
[10]   Drosophila Stem Cells Share a Common Requirement for the Histone H2B Ubiquitin Protease Scrawny [J].
Buszczak, Michael ;
Paterno, Shelley ;
Spradling, Allan C. .
SCIENCE, 2009, 323 (5911) :248-251