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靶向保护秀丽隐杆线虫内源性 microRNAs。

Target-mediated protection of endogenous microRNAs in C. elegans.

机构信息

Friedrich Miescher Institute for Biomedical Research, P.O. Box 2543, CH-4002 Basel, Switzerland.

出版信息

Dev Cell. 2011 Mar 15;20(3):388-96. doi: 10.1016/j.devcel.2011.02.008.

Abstract

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 xrn-1 (XRN1) or xrn-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.

摘要

微 RNA(miRNAs)受到转录和转录后机制的严格调控,包括核酸酶的降解。在这里,我们报告在秀丽隐杆线虫中,靶 mRNA 可以在体内保护其同源 miRNA 不被降解。我们发现 let-7(n2853) 突变通过损害这种保护作用使成熟的 let-7 miRNA 不稳定。此外,存在同源靶标或耗尽 xrn-1(XRN1)或 xrn-2(XRN2/Rat1p)外切核酶会强制积累某些 miRNA 过客(miR(∗))链。因此,在 Argonaute 中偏向 miRNA 链加载之后,消除非功能 RNA 可以进一步完善 miRNA 链选择。相反,通过将 miRNA 的水平与靶标的水平进行匹配,成熟 miRNA 降解和靶标介导的 miRNA 保护(TMMP)的相反活性可能使前体 miRNA 的两条成熟链的表达具有动态性,并且 miRNA 也可以进化。因此,mRNA 似乎不仅仅是被动的靶标,而且与 miRNA 一起在相互调节的网络中发挥作用。

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