Target-Mediated Protection of Endogenous MicroRNAs in C. elegans

被引:125
作者
Chatterjee, Saibal [1 ]
Fasler, Monika [1 ]
Buessing, Ingo [1 ]
Grosshans, Helge [1 ]
机构
[1] Friedrich Miescher Inst Biomed Res, CH-4002 Basel, Switzerland
基金
瑞士国家科学基金会; 欧洲研究理事会;
关键词
CAENORHABDITIS-ELEGANS; LET-7; MICRORNA; RNA; DROSOPHILA; SIRNAS; MECHANISMS; ASYMMETRY; COMPLEX; LIN-14;
D O I
10.1016/j.devcel.2011.02.008
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
MicroRNAs (miRNAs) are tightly regulated through transcriptional and posttranscriptional mechanisms, including degradation by nucleases. Here, we report that in C. elegans, target mRNAs can protect their cognate miRNAs from degradation in vivo. We show that the let-7(n2853) mutation destabilizes the mature let-7 miRNA by impairing this protection. Moreover, presence of a cognate target or depletion of the xm-1 (XRN1) or xm-2 (XRN2/Rat1p) exoribonucleases enforces accumulation of certain miRNA passenger (miR*) strands. Thus, following biased miRNA strand loading into Argonaute, elimination of nonfunctional RNAs can further refine miRNA strand selection. Conversely, by aligning the levels of miRNAs with those of their targets, the opposing activities of mature miRNA degradation and target-mediated miRNA protection (TMMP) may enable dynamic expression of either mature strand of a pre-miRNA, and evolution of miRNAs. Thus, it seems that mRNAs are more than inert targets and function with miRNAs in a network of mutual regulation.
引用
收藏
页码:388 / 396
页数:9
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