Spt6 Association with RNA Polymerase II Directs mRNA Turnover During Transcription

被引:35
|
作者
Dronamraju, Raghuvar [1 ,2 ]
Hepperla, Austin J. [3 ]
Shibata, Yoichiro [2 ,3 ]
Adams, Alexander T. [1 ]
Magnuson, Terry [2 ,3 ,4 ]
Davis, Ian J. [2 ,3 ,4 ,5 ]
Strahl, Brian D. [1 ,2 ,3 ]
机构
[1] Univ N Carolina, Sch Med, Dept Biochem & Biophys, Chapel Hill, NC 27599 USA
[2] Univ N Carolina, Sch Med, Lineberger Comprehens Canc Ctr, Chapel Hill, NC 27599 USA
[3] Univ N Carolina, Curriculum Genet & Mol Biol, Chapel Hill, NC 27599 USA
[4] Univ N Carolina, Carolina Ctr Genome Sci, Dept Genet, Chapel Hill, NC 27599 USA
[5] Univ N Carolina, Dept Pediat, Chapel Hill, NC 27599 USA
关键词
FACTORS REPRESS TRANSCRIPTION; ELONGATION-FACTOR SPT6; SACCHAROMYCES-CEREVISIAE; CELL-CYCLE; GENE-EXPRESSION; CHROMATIN-STRUCTURE; CCR4-NOT COMPLEX; ANTISENSE TRANSCRIPTION; GENOME-WIDE; SH2; DOMAIN;
D O I
10.1016/j.molcel.2018.05.020
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
Spt6 is an essential histone chaperone that mediates nucleosome reassembly during gene transcription. Spt6 also associates with RNA polymerase II (RNAPII) via a tandem Src2 homology domain. However, the significance of Spt6-RNAPII interaction is not well understood. Here, we show that Spt6 recruitment to genes and the nucleosome reassembly functions of Spt6 can still occur in the absence of its association with RNAPII. Surprisingly, we found that Spt6-RNAPII association is required for efficient recruitment of the Ccr4-Not de-adenylation complex to transcribed genes for essential degradation of a range of mRNAs, including mRNAs required for cell-cycle progression. These findings reveal an unexpected control mechanism for mRNA turnover during transcription facilitated by a histone chaperone.
引用
收藏
页码:1054 / +
页数:17
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