| Literature DB >> 28809393 |
Phillip J Hsu1,2,3, Yunfei Zhu4, Honghui Ma1,2, Yueshuai Guo4, Xiaodan Shi4, Yuanyuan Liu4, Meijie Qi4, Zhike Lu1,2, Hailing Shi1,2, Jianying Wang4, Yiwei Cheng4, Guanzheng Luo1,2, Qing Dai1,2, Mingxi Liu4, Xuejiang Guo4, Jiahao Sha4, Bin Shen4, Chuan He1,2,5.
Abstract
N6-methyladenosine (m6A) is the most common internal modification in eukaryotic mRNA. It is dynamically installed and removed, and acts as a new layer of mRNA metabolism, regulating biological processes including stem cell pluripotency, cell differentiation, and energy homeostasis. m6A is recognized by selective binding proteins; YTHDF1 and YTHDF3 work in concert to affect the translation of m6A-containing mRNAs, YTHDF2 expedites mRNA decay, and YTHDC1 affects the nuclear processing of its targets. The biological function of YTHDC2, the final member of the YTH protein family, remains unknown. We report that YTHDC2 selectively binds m6A at its consensus motif. YTHDC2 enhances the translation efficiency of its targets and also decreases their mRNA abundance. Ythdc2 knockout mice are infertile; males have significantly smaller testes and females have significantly smaller ovaries compared to those of littermates. The germ cells of Ythdc2 knockout mice do not develop past the zygotene stage and accordingly, Ythdc2 is upregulated in the testes as meiosis begins. Thus, YTHDC2 is an m6A-binding protein that plays critical roles during spermatogenesis.Entities:
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Year: 2017 PMID: 28809393 PMCID: PMC5587856 DOI: 10.1038/cr.2017.99
Source DB: PubMed Journal: Cell Res ISSN: 1001-0602 Impact factor: 25.617