LIN-28 and the poly(U) polymerase PUP-2 regulate let-7 microRNA processing in Caenorhabditis elegans

被引:199
作者
Lehrbach, Nicolas J. [1 ,2 ]
Armisen, Javier [1 ,2 ]
Lightfoot, Helen L. [1 ,3 ]
Murfitt, Kenneth J. [1 ]
Bugaut, Anthony [3 ]
Balasubramanian, Shankar [3 ,4 ]
Miska, Eric A. [1 ,2 ]
机构
[1] Univ Cambridge, Henry Wellcome Bldg Canc & Dev Biol, Wellcome Trust Canc Res UK Gurdon Inst, Cambridge, England
[2] Univ Cambridge, Dept Biochem, Cambridge CB2 1QW, England
[3] Univ Cambridge, Dept Chem, Cambridge CB2 1QW, England
[4] Univ Cambridge, Sch Clin Med, Cambridge CB2 1QW, England
基金
英国生物技术与生命科学研究理事会; 英国惠康基金;
关键词
C-ELEGANS; GENETIC INTERFERENCE; MESSENGER-RNA; BIOGENESIS; EXPRESSION; PATHWAY; DEGRADATION; URIDYLATION; MUTANTS; ENCODES;
D O I
10.1038/nsmb.1675
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 let-7 microRNA ( miRNA) is an ultraconserved regulator of stem cell differentiation and developmental timing and a candidate tumor suppressor. Here we show that LIN-28 and the poly( U) polymerase PUP-2 regulate let-7 processing in Caenorhabditis elegans. We demonstrate that lin-28 is necessary and sufficient to block let-7 activity in vivo; LIN-28 directly binds let-7 pre-miRNA to prevent Dicer processing. Moreover, we have identified a poly( U) polymerase, PUP-2, which regulates the stability of LIN-28 blockaded let-7 pre-miRNA and contributes to LIN-28-dependent regulation of let-7 during development. We show that PUP-2 and LIN-28 interact directly, and that LIN-28 stimulates uridylation of let-7 pre-miRNA by PUP-2 in vitro. Our results demonstrate that LIN-28 and let-7 form an ancient regulatory switch, conserved from nematodes to humans, and provide insight into the mechanism of LIN-28 action in vivo. Uridylation by a PUP-2 ortholog might regulate let-7 and additional miRNAs in other species. Given the roles of Lin28 and let-7 in stem cell and cancer biology, we propose that such poly( U) polymerases are potential therapeutic targets.
引用
收藏
页码:1016 / U27
页数:7
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