CAS Key Laboratory of Genomic and Precision Medicine, Collaborative Innovation Center of Genetics and Development, College of Future Technology, Beijing Institute of Genomics, Chinese Academy of Sciences, Beijing 100101, China; University of Chinese Academy of Sciences, Beijing 100049, China; Sino-Danish College, University of Chinese Academy of Sciences, Beijing 101408, China; Institute of Stem Cell and Regeneration, Chinese Academy of Sciences, Beijing 100101, China.
State Key Laboratory of Membrane Biology, Institute of Zoology, Chinese Academy of Sciences, Beijing 100101, China; State Key Laboratory of Experimental Hematology, Institute of Hematology and Blood Diseases Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Tianjin 300020, China.
Mol Cell. 2019 Sep 19;75(6):1188-1202.e11. doi: 10.1016/j.molcel.2019.06.033. Epub 2019 Aug 6.
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 (mC) modification in zebrafish early embryos, we found that mC-modified maternal mRNAs display higher stability than non-mC-modified mRNAs during MZT. We discovered that Y-box binding protein 1 (Ybx1) preferentially recognizes mC-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 mC-dependent manner. Our study demonstrates an unexpected mechanism of RNA mC-regulated maternal mRNA stabilization during zebrafish MZT, highlighting the critical role of mC mRNA modification in early development.
母源到合子的转变(MZT)是一个保守而基本的过程,在此过程中,通过剧烈的重编程,将母体环境转化为胚胎驱动的发育环境。然而,在 MZT 过程中,母源提供的转录本是如何动态调节的,在很大程度上仍然未知。在此,通过对斑马鱼早期胚胎 RNA 5-甲基胞嘧啶(mC)修饰的全基因组分析,我们发现 mC 修饰的母源 mRNA 在 MZT 期间比非 mC 修饰的 mRNA 具有更高的稳定性。我们发现 Y 盒结合蛋白 1(Ybx1)通过与 Ybx1 的冷休克结构域(CSD)中关键残基色氨酸 45(Trp45)的π-π相互作用,优先识别 mC 修饰的 mRNA,这在斑马鱼母源 mRNA 稳定性和早期胚胎发生中发挥着重要作用。Ybx1 与 mRNA 稳定剂 Pabpc1a 一起,以 mC 依赖性的方式促进其靶 mRNA 的稳定性。我们的研究揭示了斑马鱼 MZT 期间 RNA mC 调节的母源 mRNA 稳定的一个意外机制,强调了 mC mRNA 修饰在早期发育中的关键作用。