The 18S rRNA m6 A methyltransferase METTL5 promotes mouse embryonic stem cell differentiation

18S rRNA m6A甲基转移酶METTL5促进小鼠胚胎干细胞分化

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作者:Ming Xing #, Qi Liu #, Cong Mao, Hanyi Zeng, Xin Zhang, Shuqin Zhao, Li Chen, Mingxi Liu, Bin Shen, Xuejiang Guo, Honghui Ma, Hao Chen, Jun Zhang

Abstract

RNA modifications represent a novel layer of regulation of gene expression. Functional experiments revealed that N6 -methyladenosine (m6 A) on messenger RNA (mRNA) plays critical roles in cell fate determination and development. m6 A mark also resides in the decoding center of 18S ribosomal RNA (rRNA); however, the biological function of m6 A on 18S rRNA is still poorly understood. Here, we report that methyltransferase-like 5 (METTL5) methylates 18S rRNA both in vivo and in vitro, which is consistent with previous reports. Deletion of Mettl5 causes a dramatic differentiation defect in mouse embryonic stem cells (mESCs). Mechanistically, the m6 A deposited by METTL5 is involved in regulating the efficient translation of F-box and WD repeat domain-containing 7 (FBXW7), a key regulator of cell differentiation. Deficiency of METTL5 reduces FBXW7 levels and leads to the accumulation of its substrate c-MYC, thereby delaying the onset of mESC differentiation. Our study uncovers an important role of METTL5-mediated 18S m6 A in mESC differentiation through translation regulation and provides new insight into the functional significance of rRNA m6 A.

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