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 (... More
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.
