| Literature DB >> 33357433 |
Bowen Rong1, Qian Zhang2, Jinkai Wan1, Shenghui Xing1, Ruofei Dai1, Yuan Li3, Jiabin Cai1, Jiaying Xie1, Yang Song1, Jiawei Chen4, Lei Zhang1, Guoquan Yan1, Wen Zhang1, Hai Gao1, Jing-Dong J Han4, Qianhui Qu1, Honghui Ma5, Ye Tian6, Fei Lan7.
Abstract
N6 methylation at adenosine 1832 (m6A1832) of mammalian 18S rRNA, occupying a critical position within the decoding center, is modified by a conserved methyltransferase, METTL5. Here, we find that METTL5 shows strong substrate preference toward the 18S A1832 motif but not the other reported m6A motifs. Comparison with a yeast ribosome structural model unmodified at this site indicates that the modification may facilitate mRNA binding by inducing conformation changes in the mammalian ribosomal decoding center. METTL5 promotes p70-S6K activation and proper translation initiation, and the loss of METTL5 significantly reduces the abundance of polysome. METTL5 expression is elevated in breast cancer patient samples and is required for growth of several breast cancer cell lines. We further find that Caenorhabditis elegans lacking the homolog metl-5 develop phenotypes known to be associated with impaired translation. Altogether, our findings uncover critical and conserved roles of METTL5 in the regulation of translation.Entities:
Keywords: 18S; ER-UPR; METTL5; S6K; decoding center; lifespan; m6A1832; rRNA modification; ribosome; translation initiation
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Year: 2020 PMID: 33357433 DOI: 10.1016/j.celrep.2020.108544
Source DB: PubMed Journal: Cell Rep Impact factor: 9.423