van Wolfswinkel Josien C
Department of Molecular Cellular and Developmental Biology, Yale University, New Haven, Connecticut, USA.
Center for Stem Cell Biology, Yale School of Medicine, New Haven, Connecticut, USA.
Wiley Interdiscip Rev RNA. 2023 Aug 26:e1811. doi: 10.1002/wrna.1811.
PIWI-interacting RNAs (piRNAs) play an important role in the defense against transposons in the germline and stem cells of animals. To what extent other transcripts are also regulated by piRNAs is an ongoing topic of debate. The amount of sequence complementarity between piRNA and target that is required for effective downregulation of the targeted transcript is guiding in this discussion. Over the years, various methods have been applied to infer targeting requirements from the collections of piRNAs and potential target transcripts, and recent structural studies of the PIWI proteins have provided an additional perspective. In this review, I summarize the findings from these studies and propose a set of requirements that can be used to predict targets to the best of our current abilities. This article is categorized under: Regulatory RNAs/RNAi/Riboswitches > Regulatory RNAs RNA Interactions with Proteins and Other Molecules > Protein-RNA Interactions: Functional Implications RNA-Based Catalysis > RNA-Mediated Cleavage.
PIWI相互作用RNA(piRNA)在动物生殖系和干细胞中抵御转座子的过程中发挥着重要作用。piRNA对其他转录本的调控程度如何,仍是一个仍在争论的话题。在这场讨论中,有效下调目标转录本所需的piRNA与靶标的序列互补程度是关键所在。多年来,人们应用了各种方法从piRNA和潜在靶标转录本的集合中推断靶向需求,而最近对PIWI蛋白的结构研究又提供了一个新视角。在这篇综述中,我总结了这些研究的结果,并提出了一套要求,可用于尽我们目前所能预测靶标。本文分类如下:调控RNA/RNA干扰/核糖开关>调控RNA;RNA与蛋白质及其他分子的相互作用>蛋白质-RNA相互作用:功能影响;基于RNA的催化作用>RNA介导的切割。