作为病理性心脏重塑介质的 RNA 结合蛋白

Pooja Acharya, Sharon Parkins, Michael Tranter
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引用次数: 0

摘要

RNA 结合蛋白(RBPs)在基因表达的转录后调控中起着核心作用,可占细胞内蛋白质表达所有变化的 50%。RBPs 与目标 RNA 结合后,通常会通过调节替代性拼接、RNA 稳定/降解或核糖体装载/翻译速率来改变基因表达。所有这些转录后调控过程都已被证明在病理性心脏重塑中发挥了功能性作用,越来越多的证据开始确定单个 RBPs 及其心脏 RNA 靶点的机理贡献。本综述将重点介绍心肌细胞和成纤维细胞中依赖于 RBP 的转录后基因调控机制,以及我们目前对 RNA 结合蛋白如何在功能上促进病理性心脏重塑的理解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
RNA binding proteins as mediators of pathological cardiac remodeling
RNA binding proteins (RBPs) play a central in the post-transcriptional regulation of gene expression, which can account for up to 50% of all variations in protein expression within a cell. Following their binding to target RNAs, RBPs most typically confer changes in gene expression through modulation of alternative spicing, RNA stabilization/degradation, or ribosome loading/translation rate. All of these post-transcriptional regulatory processes have been shown to play a functional role in pathological cardiac remodeling, and a growing body of evidence is beginning to identify the mechanistic contribution of individual RBPs and their cardiac RNA targets. This review highlights the mechanisms of RBP-dependent post-transcriptional gene regulation in cardiomyocytes and fibroblasts and our current understanding of how RNA binding proteins functionally contribute to pathological cardiac remodeling.
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