Elongin A regulates transcription in vivo through enhanced RNA polymerase processivity

被引:10
作者
Wang, Yating [1 ]
Hou, Liming [1 ,4 ]
Ardehali, M. Behfar [2 ,3 ]
Kingston, Robert E. [2 ,3 ]
Dynlacht, Brian D. [1 ]
机构
[1] NYU, Sch Med, Dept Pathol, New York, NY 10016 USA
[2] Massachusetts Gen Hosp, Dept Mol Biol, Boston, MA 02114 USA
[3] Harvard Med Sch, Dept Genet, Boston, MA 02115 USA
[4] Nanjing Agr Univ, Dept Anim Genet Breeding & Reprod, Coll Anim Sci & Technol, Nanjing 210000, Jiangsu, Peoples R China
关键词
MAMMALIAN ELONGIN; ELONGATION-FACTOR; IDENTIFICATION; DEGRADATION; ACTIVATION; PROTEIN; REPEAT;
D O I
10.1074/jbc.RA120.015876
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
Elongin is an RNA polymerase II (RNAPII)-associated factor that has been shown to stimulate transcriptional elongation in vitro. The Elongin complex is thought to be required for transcriptional induction in response to cellular stimuli and to ubiquitinate RNAPII in response to DNA damage. Yet, the impact of the Elongin complex on transcription in vivo has not been well studied. Here, we performed comprehensive studies of the role of Elongin A, the largest subunit of the Elongin complex, on RNAPII transcription genome-wide. Our results suggest that Elongin A localizes to actively transcribed regions and potential enhancers, and the level of recruitment correlated with transcription levels. We also identified a large group of factors involved in transcription as Elongin A-associated factors. In addition, we found that loss of Elongin A leads to dramatically reduced levels of serine2-phosphorylated, but not total, RNAPII, and cells depleted of Elongin A show stronger promoter RNAPII pausing, suggesting that Elongin A may be involved in the release of paused RNAPII. Our RNA-seq studies suggest that loss of Elongin A did not alter global transcription, and unlike prior in vitro studies, we did not observe a dramatic impact on RNAPII elongation rates in our cell-based nascent RNA-seq experiments upon Elongin A depletion. Taken together, our studies provide the first comprehensive analysis of the role of Elongin A in regulating transcription in vivo. Our studies also revealed that unlike prior in vitro findings, depletion of Elongin A has little impact on global transcription profiles and transcription elongation in vivo.
引用
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页数:12
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