互补靶标如何在靶向microRNA降解过程中暴露microRNA 3'端进行尾尾和修剪。

Paulina Pawlica, Jessica Sheu-Gruttadauria, Ian J MacRae, Joan A Steitz
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引用次数: 19

摘要

microRNAs (miRNAs)是信使rna转录后调控的关键。“经典”miRNA靶点主要与位于miRNA 5'端附近的miRNA种子序列相互作用。有趣的是,某些转录本与miRNAs 3'区表现出广泛的互补性,而不是受到调节,诱导miRNA在一个称为靶定向miRNA降解(TDMD)的过程中衰变。本文综述了近年来在TDMD分子机制方面的研究进展。具体来说,我们讨论了miRNA与tdmd诱导靶点的广泛互补如何导致miRNA 3'端从Argonaute蛋白的保护口袋中移位。然后,未受保护的miRNA 3'端可被尚未识别的细胞酶酶攻击。鉴定这些细胞酶和发现额外的tdmd诱导转录物是未来研究的主题。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

How Complementary Targets Expose the microRNA 3' End for Tailing and Trimming during Target-Directed microRNA Degradation.

How Complementary Targets Expose the microRNA 3' End for Tailing and Trimming during Target-Directed microRNA Degradation.

How Complementary Targets Expose the microRNA 3' End for Tailing and Trimming during Target-Directed microRNA Degradation.

microRNAs (miRNAs) are crucial for posttranscriptional regulation of messenger RNAs. "Classical" miRNA targets predominantly interact with the miRNA seed sequence located near the miRNA 5' end. Interestingly, certain transcripts that exhibit extensive complementarity to the miRNAs 3' region, instead of being subjected to regulation, induce miRNA decay in a process termed target-directed miRNA degradation (TDMD). Here, we review recent advances in understanding the molecular mechanisms of TDMD. Specifically, we discuss how extensive miRNA complementarity to TDMD-inducing targets results in displacement of the miRNA 3' end from its protective pocket in the Argonaute protein. Unprotected miRNA 3' ends are then available for enzymatic attack by still-unidentified cellular enzymes. Identification of these cellular enzymes and discovery of additional TDMD-inducing transcripts are subjects for future research.

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