LIN41 Post-transcriptionally Silences mRNAs by Two Distinct and Position-Dependent Mechanisms

被引:57
作者
Aeschimann, Florian [1 ,2 ]
Kumari, Pooja [1 ]
Bartake, Hrishikesh [1 ,2 ]
Gaidatzis, Dimos [1 ,3 ]
Xu, Lan [1 ]
Ciosk, Rafal [1 ]
Grosshans, Helge [1 ]
机构
[1] Friedrich Miescher Inst Biomed Res, Maulbeerstr 66, CH-4058 Basel, Switzerland
[2] Univ Basel, Fac Sci, CH-4056 Basel, Switzerland
[3] Swiss Inst Bioinformat, CH-4058 Basel, Switzerland
基金
瑞士国家科学基金会; 欧洲研究理事会;
关键词
DIFFERENTIATION FACTOR LIN-29; CAENORHABDITIS-ELEGANS; TERMINAL DIFFERENTIATION; GENE-EXPRESSION; NHL-DOMAIN; TRANSLATIONAL CONTROL; UBIQUITIN LIGASE; LET-7; PROTEIN; TRANSITION;
D O I
10.1016/j.molcel.2016.12.010
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 RNA-binding protein (RBP) LIN41, also known as LIN-41 or TRIM71, is a key regulator of animal development, but its physiological targets and molecular mechanism of action are largely elusive. Here we find that this RBP has two distinct mRNA-silencing activities. Using genome-wide ribosome profiling, RNA immunoprecipitation, and in vitro-binding experiments, we identify four mRNAs, each encoding a transcription factor or cofactor, as direct physiological targets of C. elegans LIN41. LIN41 silences three of these targets through their 30 UTRs, but it achieves isoform-specific silencing of one target, lin-29A, through its unique 50 UTR. Whereas the 30 UTR targets mab-10, mab-3, and dmd-3 undergo transcript degradation, lin-29A experiences translational repression. Through binding site transplantation experiments, we demonstrate that it is the location of the LIN41-binding site that specifies the silencing mechanism. Such position-dependent dual activity may, when studied more systematically, emerge as a feature shared by other RBPs.
引用
收藏
页码:476 / +
页数:18
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