The Human PAF1 Complex Acts in Chromatin Transcription Elongation Both Independently and Cooperatively with SII/TFIIS

被引:216
作者
Kim, Jaehoon [1 ]
Guermah, Mohamed [1 ]
Roeder, Robert G. [1 ]
机构
[1] Rockefeller Univ, Biochem & Mol Biol Lab, New York, NY 10065 USA
关键词
RNA-POLYMERASE-II; SACCHAROMYCES-CEREVISIAE; HISTONE METHYLATION; H2B UBIQUITYLATION; GENE-EXPRESSION; IN-VIVO; RTF1; INITIATION; NUCLEOSOMES; COMPONENT;
D O I
10.1016/j.cell.2009.12.050
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
Genetic and cell-based studies have implicated the PAF1 complex (PAF1C) in transcription-associated events, but there has been no evidence showing a direct role in facilitating transcription of a natural chromatin template. Here, we demonstrate an intrinsic ability of human PAF1C (hPAF1C) to facilitate activator (p53)- and histone acetyltransferase (p300)-dependent transcription elongation from a recombinant chromatin template in a biochemically defined RNA polymerase II transcription system. This represents a PAF1C function distinct from its established role in histone ubiquitylation and methylation. Importantly, we further demonstrate a strong synergy between hPAF1C and elongation factor SII/TFIIS and an underlying mechanism involving direct hPAF1C-SII interactions and cooperative binding to RNA polymerase II. Apart from a distinct PAF1C function, the present observations provide a molecular mechanism for the cooperative function of distinct transcription elongation factors in chromatin transcription.
引用
收藏
页码:491 / 503
页数:13
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