| Literature DB >> 31399345 |
Ying Yang1, Lu Wang2, Xiao Han3, Wen-Lan Yang3, Mengmeng Zhang4, Hai-Li Ma5, Bao-Fa Sun1, Ang Li5, Jun Xia6, Jing Chen5, Jian Heng6, Baixing Wu4, Yu-Sheng Chen5, Jia-Wei Xu7, Xin Yang5, Huan Yao5, Jiawei Sun8, Cong Lyu9, Hai-Lin Wang10, Ying Huang11, Ying-Pu Sun7, Yong-Liang Zhao1, Anming Meng8, Jinbiao Ma12, Feng Liu13, Yun-Gui Yang14.
Abstract
The maternal-to-zygotic transition (MZT) is a conserved and fundamental process during which the maternal environment is converted to an environment of embryonic-driven development through dramatic reprogramming. However, how maternally supplied transcripts are dynamically regulated during MZT remains largely unknown. Herein, through genome-wide profiling of RNA 5-methylcytosine (m5C) modification in zebrafish early embryos, we found that m5C-modified maternal mRNAs display higher stability than non-m5C-modified mRNAs during MZT. We discovered that Y-box binding protein 1 (Ybx1) preferentially recognizes m5C-modified mRNAs through π-π interactions with a key residue, Trp45, in Ybx1's cold shock domain (CSD), which plays essential roles in maternal mRNA stability and early embryogenesis of zebrafish. Together with the mRNA stabilizer Pabpc1a, Ybx1 promotes the stability of its target mRNAs in an m5C-dependent manner. Our study demonstrates an unexpected mechanism of RNA m5C-regulated maternal mRNA stabilization during zebrafish MZT, highlighting the critical role of m5C mRNA modification in early development.Entities:
Keywords: 5-methylcytosine; Pabpc1a; RNA methylation; Ybx1; cold shock domain; early embryogenesis; maternal mRNA decay; maternal-to-zygotic transition; zebrafish; π-π interactions
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Year: 2019 PMID: 31399345 DOI: 10.1016/j.molcel.2019.06.033
Source DB: PubMed Journal: Mol Cell ISSN: 1097-2765 Impact factor: 17.970