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综合征型和非综合征型疾病相关的 Cx43 突变。

Syndromic and non-syndromic disease-linked Cx43 mutations.

机构信息

Department of Anatomy and Cell Biology, University of Western Ontario, London, Ontario N6A 5C1, Canada; Department of Physiology and Pharmacology, University of Western Ontario, London, Ontario N6A 5C1, Canada.

出版信息

FEBS Lett. 2014 Apr 17;588(8):1339-48. doi: 10.1016/j.febslet.2013.12.022. Epub 2014 Jan 14.

Abstract

There are now at least 14 distinct diseases linked to germ line mutations in the 21 genes that encode the connexin (Cx) family of gap junction proteins. This review focuses on the links between germ-line mutations in the gene encoding Cx43 (GJA1) and the human disease termed oculodentodigital dysplasia (ODDD). This disease is clinically characterized by soft tissue fusion of the digits, abnormal craniofacial bone development, small eyes and loss of tooth enamel. However, the disease is considerably more complex and somewhat degenerative as patients often suffer from other syndromic effects that include incontinence, glaucoma, skin diseases and neuropathies that become more pronounced during aging. The challenge continues to be understanding how distinct Cx43 gene mutations cause such a diverse range of tissue phenotypes and pathophysiological changes while other Cx43-rich organs are relatively unaffected. This review will provide an overview of many of these studies and distill some themes and outstanding questions that need to be addressed in the coming years.

摘要

现在至少有 14 种不同的疾病与编码间隙连接蛋白家族的 21 个基因中的种系突变有关。本综述重点介绍了编码连接蛋白 43 (GJA1) 的基因突变与人类疾病眼-牙-指发育不良 (ODDD) 之间的联系。这种疾病的临床特征是手指软组织融合、颅面骨发育异常、眼睛小和牙釉质丧失。然而,这种疾病要复杂得多,而且有些退化,因为患者经常患有其他综合征效应,包括尿失禁、青光眼、皮肤病和神经病,这些在衰老过程中变得更加明显。挑战仍然是理解不同的 Cx43 基因突变如何导致如此广泛的组织表型和病理生理变化,而其他富含 Cx43 的器官相对不受影响。本综述将概述其中的许多研究,并提炼出一些主题和悬而未决的问题,这些问题需要在未来几年解决。

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