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非典型 microRNA 特征:心血管疾病中的新兴范例。

Non-canonical features of microRNAs: paradigms emerging from cardiovascular disease.

机构信息

Institute for Cardiovascular Prevention (IPEK), Ludwig-Maximilians-Universität (LMU), Munich, Germany.

German Center for Cardiovascular Research (DZHK), partner site Munich Heart Alliance, Munich, Germany.

出版信息

Nat Rev Cardiol. 2022 Sep;19(9):620-638. doi: 10.1038/s41569-022-00680-2. Epub 2022 Mar 18.

DOI:10.1038/s41569-022-00680-2
PMID:35304600
Abstract

Research showing that microRNAs (miRNAs) are versatile regulators of gene expression has instigated tremendous interest in cardiovascular research. The overwhelming majority of studies are predicated on the dogmatic notion that miRNAs regulate the expression of specific target mRNAs by inhibiting mRNA translation or promoting mRNA decay in the RNA-induced silencing complex (RISC). These efforts mostly identified and dissected contributions of multiple regulatory networks of miRNA-target mRNAs to cardiovascular pathogenesis. However, evidence from studies in the past decade indicates that miRNAs also operate beyond this canonical paradigm, featuring non-conventional regulatory functions and cellular localizations that have a pathophysiological role in cardiovascular disease. In this Review, we highlight the functional relevance of atypical miRNA biogenesis and localization as well as RISC heterogeneity. Moreover, we delineate remarkable non-canonical examples of miRNA functionality, including direct interactions with proteins beyond the Argonaute family and their role in transcriptional regulation in the nucleus and in mitochondria. We scrutinize the relevance of non-conventional biogenesis and non-canonical functions of miRNAs in cardiovascular homeostasis and pathology, and contextualize how uncovering these non-conventional properties can expand the scope of translational research in the cardiovascular field and beyond.

摘要

研究表明,微小 RNA(miRNA)是基因表达的多功能调节剂,这激发了人们对心血管研究的极大兴趣。绝大多数研究都基于一种教条式的观点,即 miRNA 通过抑制 mRNA 翻译或促进 RNA 诱导沉默复合物(RISC)中的 mRNA 降解来调节特定靶 mRNA 的表达。这些努力主要确定并剖析了 miRNA-靶 mRNA 的多个调控网络对心血管发病机制的贡献。然而,过去十年的研究证据表明,miRNA 的作用也超出了这一典型模式,具有非传统的调控功能和细胞定位,在心血管疾病中具有病理生理学作用。在这篇综述中,我们强调了非典型 miRNA 生物发生和定位以及 RISC 异质性的功能相关性。此外,我们还描述了 miRNA 功能的显著非典型实例,包括与 Argonaute 家族以外的蛋白质的直接相互作用及其在核和线粒体中转录调控中的作用。我们仔细研究了非典型生物发生和 miRNA 非典型功能在心血管稳态和病理学中的相关性,并将揭示这些非典型特性如何扩展心血管领域及其他领域转化研究的范围。

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