The m6A Methyltransferase METTL3 Promotes Translation in Human Cancer Cells

被引:1171
|
作者
Lin, Shuibin [1 ,2 ]
Choe, Junho [1 ,2 ]
Du, Peng [1 ,2 ]
Triboulet, Robinson [1 ,2 ]
Gregory, Richard I. [1 ,2 ,3 ,4 ]
机构
[1] Boston Childrens Hosp, Div Hematol Oncol, Stem Cell Program, Boston, MA 02115 USA
[2] Harvard Univ, Sch Med, Dept Biol Chem & Mol Pharmacol, Boston, MA 02115 USA
[3] Harvard Univ, Sch Med, Dept Pediat, Boston, MA 02115 USA
[4] Harvard Univ, Harvard Stem Cell Inst, Cambridge, MA 02138 USA
关键词
MESSENGER-RNA METHYLATION; NUCLEAR-RNA; YTH DOMAIN; IN-VITRO; N-6-METHYLADENOSINE; EXPRESSION; REVEALS; COMPLEX; BINDING; N6-METHYLADENOSINE;
D O I
10.1016/j.molcel.2016.03.021
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
METTL3 is an RNA methyltransferase implicated in mRNA biogenesis, decay, and translation control through N-6-methyladenosine (m(6)A) modification. Here we find that METTL3 promotes translation of certain mRNAs including epidermal growth factor receptor (EGFR) and the Hippo pathway effector TAZ in human cancer cells. In contrast to current models that invoke m(6)A reader proteins downstream of nuclear METTL3, we find METTL3 associates with ribosomes and promotes translation in the cytoplasm. METTL3 depletion inhibits translation, and both wild-type and catalytically inactive METTL3 promote translation when tethered to a reporter mRNA. Mechanistically, METTL3 enhances mRNA translation through an interaction with the translation initiation machinery. METTL3 expression is elevated in lung adenocarcinoma and using both loss-and gain-of-function studies, we find that METTL3 promotes growth, survival, and invasion of human lung cancer cells. Our results uncover an important role of METTL3 in promoting translation of oncogenes in human lung cancer.
引用
收藏
页码:335 / 345
页数:11
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