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小 RNA 找到它们的靶标:当甲基化保护 miRNA 免受尿嘧啶化时。

Small RNAs meet their targets: when methylation defends miRNAs from uridylation.

机构信息

a State Key Laboratory of Genetic Engineering and Collaborative Innovation Center for Genetics and Development; Institute of Plant Biology; School of Life Sciences; Fudan University ; Shanghai , China.

出版信息

RNA Biol. 2014;11(9):1099-104. doi: 10.4161/rna.36243.

Abstract

Small RNAs are incorporated into Argonaute protein-containing complexes to guide the silencing of target RNAs in both animals and plants. The abundance of endogenous small RNAs is precisely controlled at multiple levels including transcription, processing and Argonaute loading. In addition to these processes, 3' end modification of small RNAs, the topic of a research area that has rapidly evolved over the last several years, adds another layer of regulation of their abundance, diversity and function. Here, we review our recent understanding of small RNA 3' end methylation and tailing.

摘要

小 RNA 被整合到含有 Argonaute 蛋白的复合物中,以指导动植物中靶 RNA 的沉默。内源性小 RNA 的丰度在转录、加工和 Argonaute 加载等多个水平上受到精确控制。除了这些过程,小 RNA 的 3'端修饰——这是过去几年快速发展的研究领域的主题——为它们的丰度、多样性和功能增加了另一层调控。在这里,我们回顾了我们最近对小 RNA 3'端甲基化和加尾的理解。

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