Acharya Pooja, Parkins Sharon, Tranter Michael
Department of Molecular Medicine and Therapeutics, The Ohio State University Wexner Medical Center, Columbus, OH, United States.
Dorothy M. Davis Heart and Lung Research Institute, The Ohio State University Wexner Medical Center, Columbus, OH, United States.
Front Cell Dev Biol. 2024 May 16;12:1368097. doi: 10.3389/fcell.2024.1368097. eCollection 2024.
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.
RNA结合蛋白(RBPs)在基因表达的转录后调控中起着核心作用,这可占细胞内蛋白质表达所有变化的50%。RBPs与靶RNA结合后,最典型的是通过调节可变剪接、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已被证明在病理性心脏重塑中发挥功能作用,越来越多的证据开始确定单个RBPs及其心脏RNA靶标的机制性作用。本综述重点介绍了心肌细胞和成纤维细胞中RBP依赖性转录后基因调控的机制,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。