Evidence that Lin28 stimulates translation by recruiting RNA helicase A to polysomes

被引:82
作者
Jin, Jianyu [1 ,2 ]
Jing, Wei [3 ]
Lei, Xin-Xiang [1 ,2 ]
Feng, Chen [1 ,4 ]
Peng, Shuping [1 ]
Boris-Lawrie, Kathleen [3 ]
Huang, Yingqun [1 ]
机构
[1] Yale Univ, Sch Med, Dept Obstet Gynecol & Reprod Sci, New Haven, CT 06510 USA
[2] Wenzhou Univ, Coll Teacher Educ, Dept Chem, Wenzhou 325035, Zhejiang, Peoples R China
[3] Ohio State Univ, Ctr Retrovirus Res, Ctr RNA Biol, Dept Vet Biosci, Columbus, OH 43210 USA
[4] China Med Univ, Dept Biochem & Mol Biol, Shenyang 110001, Liaoning, Peoples R China
基金
美国国家卫生研究院;
关键词
LET-7; MICRORNA; MESSENGER-RNA; LIN-28; EXPRESSION; REGULATOR; BIOGENESIS; INTERACTS; CELLS; RU5;
D O I
10.1093/nar/gkq1350
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
The stem cell protein Lin28 functions to inhibit the biogenesis of a group of miRNAs but also stimulates the expression of a subset of mRNAs at the post-transcriptional level, the underlying mechanism of which is not yet understood. Here we report the characterization of the molecular interplay between Lin28 and RNA helicase A (RHA) known to play an important role in remodeling ribonucleoprotein particles during translation. We show that reducing Lin28 expression results in decreased RHA association with polysomes while increasing Lin28 expression leads to elevated RHA association. Further, the carboxyl terminus of Lin28 is necessary for interaction with both the amino and carboxyl termini of RHA. Importantly, a carboxyl terminal deletion mutant of Lin28 that retains RNA-binding activity fails to interact with RHA and exhibits dominant-negative effects on Lin28-dependent stimulation of translation. Taken together, these results lead us to suggest that Lin28 may stimulate translation by actively recruiting RHA to polysomes.
引用
收藏
页码:3724 / 3734
页数:11
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