Ribosomal protein RPS-14 modulates let-7 microRNA function in Caenorhabditis elegans

被引:22
作者
Chan, Shih-Peng [1 ]
Slack, Frank J. [1 ]
机构
[1] Yale Univ, Dept Mol Cellular & Dev Biol, New Haven, CT 06520 USA
关键词
MicroRNA; let-7; RPS-14; Ribosome; Stem cell; C; elegans; C-ELEGANS; MESSENGER-RNAS; TRANSLATION INITIATION; POSTTRANSCRIPTIONAL REGULATION; REPRESS TRANSLATION; ANIMAL DEVELOPMENT; CELL LINEAGES; IN-VITRO; MECHANISMS; DROSOPHILA;
D O I
10.1016/j.ydbio.2009.07.011
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
The let-7 microRNA (miRNA) regulates developmental timing at the larval-to-adult transition in Caenorhabditis elegans. Dysregulation of let-7 results in irregular hypodermal and vulval development. Disrupted let-7 function is also a feature of human lung cancer. However, little is known about the mechanism and co-factors of let-7. Here we demonstrate that ribosomal protein RPS-14 is able to modulate let-7 function in C. elegans. The RPS-14 protein co-immunoprecipitated with the nematode Argonaute homolog, ALG-1. Reduction of rps-14 gene expression by RNAi suppressed the aberrant vulva and hypodermis development phenotypes of let-7(n2853) mutant animals and the mis-regulation of a reporter bearing the lin-41 3'UTR, a well established let-7 target. Our results indicate an interactive relationship between let-7 miRNA function and ribosomal protein RPS-14 in regulation of terminal differentiation that may help in understanding the mechanism of translational control by miRNAs. (C) 2009 Elsevier Inc. All rights reserved.
引用
收藏
页码:152 / 160
页数:9
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