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ALYREF links 3′-end processing to nuclear export of non-polyadenylated mRNAs

  • Jing Fan
  • , Ke Wang
  • , Xian Du
  • , Jianshu Wang
  • , Suli Chen
  • , Yimin Wang
  • , Min Shi
  • , Li Zhang
  • , Xudong Wu
  • , Dinghai Zheng
  • , Changshou Wang
  • , Lantian Wang
  • , Bin Tian
  • , Guohui Li
  • , Yu Zhou
  • , Hong Cheng
  • University of Chinese Academy of Sciences
  • Wuhan University
  • Dalian Institute of Chemical Physics Chinese Academy of Sciences
  • Rutgers New Jersey Medical School

科研成果: 期刊稿件文章同行评审

48 引用 (Scopus)

摘要

The RNA-binding protein ALYREF plays key roles in nuclear export and also 3′-end processing of polyadenylated mRNAs, but whether such regulation also extends to non-polyadenylated RNAs is unknown. Replication-dependent (RD)-histone mRNAs are not polyadenylated, but instead end in a stem-loop (SL) structure. Here, we demonstrate that ALYREF prevalently binds a region next to the SL on RD-histone mRNAs. SL-binding protein (SLBP) directly interacts with ALYREF and promotes its recruitment. ALYREF promotes histone pre-mRNA 3′-end processing by facilitating U7-snRNP recruitment through physical interaction with the U7-snRNP-specific component Lsm11. Furthermore, ALYREF, together with other components of the TREX complex, enhances histone mRNA export. Moreover, we show that 3′-end processing promotes ALYREF recruitment and histone mRNA export. Together, our results point to an important role of ALYREF in coordinating 3′-end processing and nuclear export of non-polyadenylated mRNAs.

源语言英语
文章编号e99910
期刊EMBO Journal
38
9
DOI
出版状态已出版 - 2 5月 2019
已对外发布

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