眼睛缺失家族:DNA 修复、有丝分裂和复制的交叉点

IF 3 3区 生物学 Q2 GENETICS & HEREDITY
Christopher B. Nelson, Jadon K. Wells, Hilda A. Pickett
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引用次数: 0

摘要

无眼家族(EYA1-4)是一组具有双重功能的蛋白质,既是酪氨酸磷酸酶,又是转录协同激活因子。EYA 蛋白在发育过程中起着至关重要的作用,但在癌症中也会出现异常过表达,它们通常会产生致癌作用。随着 EYA 抑制剂的治疗潜力不断扩大,人们对 EYA 如何精确影响细胞生物学的兴趣与日俱增。最近的功能性研究表明,EYAs 是调控基因组维护途径(包括 DNA 修复、有丝分裂和 DNA 复制)的重要角色。虽然表征的分子机制主要归因于 EYA 磷酸酶活性,但也发现 EYA 共转录活性会影响支持这些途径的基因的表达。这表明 EYA 磷酸酶和共转录活性在功能上趋于一致,突出了 EYA 蛋白家族在基因组维护机制交叉点上新出现的重要性。在这篇综述中,我们讨论了最近在确定 EYA 蛋白底物和转录效应方面取得的进展,特别是在基因组维护方面。然后,我们概述了该领域的未来发展方向,并讨论了 EYA 抑制剂的临床用途。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The Eyes Absent family: At the intersection of DNA repair, mitosis, and replication

The Eyes Absent family (EYA1–4) are a group of dual function proteins that act as both tyrosine phosphatases and transcriptional co-activators. EYA proteins play a vital role in development, but are also aberrantly overexpressed in cancers, where they often confer an oncogenic effect. Precisely how the EYAs impact cell biology is of growing interest, fuelled by the therapeutic potential of an expanding repertoire of EYA inhibitors. Recent functional studies suggest that the EYAs are important players in the regulation of genome maintenance pathways including DNA repair, mitosis, and DNA replication. While the characterized molecular mechanisms have predominantly been ascribed to EYA phosphatase activities, EYA co-transcriptional activity has also been found to impact the expression of genes that support these pathways. This indicates functional convergence of EYA phosphatase and co-transcriptional activities, highlighting the emerging importance of the EYA protein family at the intersection of genome maintenance mechanisms. In this review, we discuss recent progress in defining EYA protein substrates and transcriptional effects, specifically in the context of genome maintenance. We then outline future directions relevant to the field and discuss the clinical utility of EYA inhibitors.

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来源期刊
DNA Repair
DNA Repair 生物-毒理学
CiteScore
7.60
自引率
5.30%
发文量
91
审稿时长
59 days
期刊介绍: DNA Repair provides a forum for the comprehensive coverage of DNA repair and cellular responses to DNA damage. The journal publishes original observations on genetic, cellular, biochemical, structural and molecular aspects of DNA repair, mutagenesis, cell cycle regulation, apoptosis and other biological responses in cells exposed to genomic insult, as well as their relationship to human disease. DNA Repair publishes full-length research articles, brief reports on research, and reviews. The journal welcomes articles describing databases, methods and new technologies supporting research on DNA repair and responses to DNA damage. Letters to the Editor, hot topics and classics in DNA repair, historical reflections, book reviews and meeting reports also will be considered for publication.
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