肌盲样蛋白家族的功能及其在疾病中的作用。

IF 8.2 2区 生物学 Q1 CELL BIOLOGY
Hui Zhou, Jiachi Xu, Liusheng Pan
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引用次数: 0

摘要

保守蛋白的特点是其功能在整个进化历史中几乎保持不变,无论是纵向的时间还是横向的物种。在这篇综述中,我们重点介绍了一类被称为MBNL家族的保守蛋白。作为RNA结合蛋白,MBNL家族成员通过进化保守的串联锌指结构域与pre-mRNA相互作用,并在多种RNA代谢过程中发挥关键作用,包括选择性剪接、mRNA稳定性、转运、亚细胞定位调控和选择性聚腺苷化。MBNL蛋白的失调会导致严重的后果。最初,研究主要将MBNL蛋白与肌强直性营养不良联系起来。然而,最近的研究表明,它们参与了广泛的生理和病理过程,如胚胎组织分化和循环系统疾病。此外,MBNL蛋白在癌症中的新兴作用揭示了这些进化上古老的蛋白的一个新的方面。本文对MBNL家族进行了综述,重点介绍了其结构、生物学功能机制及其在各种疾病中的作用。主题术语:肌盲样蛋白,rna结合蛋白,选择性剪接,肿瘤,肌强直性营养不良。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Functions of the Muscleblind-like protein family and their role in disease.

Conserved proteins are characterized by their functions remaining nearly constant throughout evolutionary history, both vertically through time and horizontally across species. In this review, we focus on a class of conserved proteins known as the Muscleblind-like (MBNL) family. As RNA-binding proteins, MBNL family members interact with pre-mRNAs through evolutionarily conserved tandem zinc finger domains and play critical roles in various RNA metabolic processes, including alternative splicing, mRNA stability, trafficking, regulation of subcellular localization, and alternative polyadenylation. Dysregulation of MBNL proteins can lead to severe consequences. Initially, research primarily associated MBNL proteins with myotonic dystrophy. However, recent studies have revealed their involvement in a broad spectrum of physiological and pathological processes, such as embryonic tissue differentiation and circulatory disorders. Furthermore, the emerging role of MBNL proteins in cancer sheds light on a novel aspect of these evolutionarily ancient proteins. This review provides a comprehensive overview of the MBNL family, emphasizing its structure, the mechanisms underlying its biological functions, and its roles in various diseases.Subject terms: Muscleblind-like-like protein, RNA-binding proteins, Alternative splicing, Tumor, Myotonic dystrophy.

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来源期刊
CiteScore
11.00
自引率
0.00%
发文量
180
期刊介绍: Cell Communication and Signaling (CCS) is a peer-reviewed, open-access scientific journal that focuses on cellular signaling pathways in both normal and pathological conditions. It publishes original research, reviews, and commentaries, welcoming studies that utilize molecular, morphological, biochemical, structural, and cell biology approaches. CCS also encourages interdisciplinary work and innovative models, including in silico, in vitro, and in vivo approaches, to facilitate investigations of cell signaling pathways, networks, and behavior. Starting from January 2019, CCS is proud to announce its affiliation with the International Cell Death Society. The journal now encourages submissions covering all aspects of cell death, including apoptotic and non-apoptotic mechanisms, cell death in model systems, autophagy, clearance of dying cells, and the immunological and pathological consequences of dying cells in the tissue microenvironment.
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