5-methylcytosine promotes mRNA export — NSUN2 as the methyltransferase and ALYREF as an m5C reader

Xin Yang(Beijing Institute of Genomics), Ying Yang(University of Chinese Academy of Sciences), Baofa Sun(Beijing Institute of Genomics), Yusheng Chen(Chinese Academy of Sciences), Jiawei Xu(First Affiliated Hospital of Zhengzhou University), Weiyi Lai(University of Chinese Academy of Sciences), Ang Li(Beijing Institute of Genomics), Xing Wang(University of Chinese Academy of Sciences), Devi Prasad Bhattarai(Chinese Academy of Sciences), Wen Xiao(Beijing Institute of Genomics), Huiying Sun(Chinese Academy of Sciences), Qin Zhu(Beijing Institute of Genomics), Haili Ma(Chinese Academy of Sciences), Samir Adhikari(Chinese Academy of Sciences), Min Sun(Chinese Academy of Sciences), Yajuan Hao(Beijing Institute of Genomics), Bing Zhang(Beijing Institute of Genomics), Chun-Min Huang(Chinese Academy of Sciences), Niu Huang(National Institute of Biological Sciences, Beijing), Guibin Jiang(Research Center for Eco-Environmental Sciences), Yongliang Zhao(Chinese Academy of Sciences), Hailin Wang(Chinese Academy of Sciences), Yingpu Sun(First Affiliated Hospital of Zhengzhou University), Yun‐Gui Yang(Chinese Academy of Sciences)
Cell Research
April 18, 2017
Cited by 1,169Open Access
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Abstract

5-methylcytosine (m5C) is a post-transcriptional RNA modification identified in both stable and highly abundant tRNAs and rRNAs, and in mRNAs. However, its regulatory role in mRNA metabolism is still largely unknown. Here, we reveal that m5C modification is enriched in CG-rich regions and in regions immediately downstream of translation initiation sites and has conserved, tissue-specific and dynamic features across mammalian transcriptomes. Moreover, m5C formation in mRNAs is mainly catalyzed by the RNA methyltransferase NSUN2, and m5C is specifically recognized by the mRNA export adaptor ALYREF as shown by in vitro and in vivo studies. NSUN2 modulates ALYREF's nuclear-cytoplasmic shuttling, RNA-binding affinity and associated mRNA export. Dysregulation of ALYREF-mediated mRNA export upon NSUN2 depletion could be restored by reconstitution of wild-type but not methyltransferase-defective NSUN2. Our study provides comprehensive m5C profiles of mammalian transcriptomes and suggests an essential role for m5C modification in mRNA export and post-transcriptional regulation.


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