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SR proteins collaborate with 7SK and promoter-associated nascent RNA to release paused polymerase

  • Xiong Ji
  • , Yu Zhou
  • , Shatakshi Pandit
  • , Jie Huang
  • , Hairi Li
  • , Charles Y. Lin
  • , Rui Xiao
  • , Christopher B. Burge
  • , Xiang Dong Fu
  • Wuhan University
  • University of California
  • Massachusetts Institute of Technology
  • University of California at San Diego

科研成果: 期刊稿件文章同行评审

281 引用 (Scopus)

摘要

RNAP II is frequently paused near gene promoters in mammals, and its transition to productive elongation requires active recruitment of P-TEFb, a cyclin-dependent kinase for RNAP II and other key transcription elongation factors. A fraction of P-TEFb is sequestered in an inhibitory complex containing the 7SK noncoding RNA, but it has been unclear how P-TEFb is switched from the 7SK complex to RNAP II during transcription activation. We report that SRSF2 (also known as SC35, an SR-splicing factor) is part of the 7SK complex assembled at gene promoters and plays a direct role in transcription pause release. We demonstrate RNA-dependent, coordinated release of SRSF2 and P-TEFb from the 7SK complex and transcription activation via SRSF2 binding to promoter-associated nascent RNA. These findings reveal an unanticipated SR protein function, a role for promoter-proximal nascent RNA in gene activation, and an analogous mechanism to HIV Tat/TAR for activating cellular genes.

源语言英语
页(从-至)855-868
页数14
期刊Cell
153
4
DOI
出版状态已出版 - 9 5月 2013
已对外发布

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