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人类发育与疾病中的T-Box基因

T-Box Genes in Human Development and Disease.

作者信息

Ghosh T K, Brook J D, Wilsdon A

机构信息

School of Life Sciences, Queens Medical Centre, University of Nottingham, Nottingham, United Kingdom.

School of Life Sciences, Queens Medical Centre, University of Nottingham, Nottingham, United Kingdom.

出版信息

Curr Top Dev Biol. 2017;122:383-415. doi: 10.1016/bs.ctdb.2016.08.006. Epub 2016 Oct 5.

DOI:10.1016/bs.ctdb.2016.08.006
PMID:28057271
Abstract

T-box genes are important development regulators in vertebrates with specific patterns of expression and precise roles during embryogenesis. They encode transcription factors that regulate gene transcription, often in the early stages of development. The hallmark of this family of proteins is the presence of a conserved DNA binding motif, the "T-domain." Mutations in T-box genes can cause developmental disorders in humans, mostly due to functional deficiency of the relevant proteins. Recent studies have also highlighted the role of some T-box genes in cancer and in cardiomyopathy, extending their role in human disease. In this review, we focus on ten T-box genes with a special emphasis on their roles in human disease.

摘要

T-box基因是脊椎动物中重要的发育调节因子,在胚胎发生过程中具有特定的表达模式和精确的作用。它们编码转录因子,通常在发育的早期阶段调节基因转录。该蛋白家族的标志是存在保守的DNA结合基序,即“T结构域”。T-box基因的突变可导致人类发育障碍,主要是由于相关蛋白质的功能缺陷。最近的研究还强调了一些T-box基因在癌症和心肌病中的作用,扩展了它们在人类疾病中的作用。在这篇综述中,我们重点关注十个T-box基因,特别强调它们在人类疾病中的作用。

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