| Literature DB >> 30858280 |
Jing Fan1, Ke Wang1, Xian Du2, Jianshu Wang1, Suli Chen1, Yimin Wang1, Min Shi1, Li Zhang1, Xudong Wu3, Dinghai Zheng4, Changshou Wang1, Lantian Wang1, Bin Tian4, Guohui Li3, Yu Zhou2, Hong Cheng5.
Abstract
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.Entities:
Keywords: zzm321990ALYREFzzm321990; zzm321990SLBPzzm321990; 3′‐end processing; RD‐histone mRNA; mRNA export
Mesh:
Substances:
Year: 2019 PMID: 30858280 PMCID: PMC6484419 DOI: 10.15252/embj.201899910
Source DB: PubMed Journal: EMBO J ISSN: 0261-4189 Impact factor: 11.598