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角蛋白5螺旋终止肽中的一种新型突变导致单纯性大疱性表皮松解症Dowling-Meara型。

A novel mutation in the helix termination peptide of keratin 5 causing epidermolysis bullosa simplex Dowling-Meara.

作者信息

Irvine A D, McKenna K E, Bingham A, Nevin N C, Hughes A E

机构信息

Department of Medical Genetics, The Queen's University of Belfast, Northern Ireland, UK.

出版信息

J Invest Dermatol. 1997 Dec;109(6):815-6. doi: 10.1111/1523-1747.ep12341024.

Abstract

Epidermolysis bullosa simplex Dowling-Meara (MIM# 1317600) is the most severe of the three common epidermolysis bullosa simplex subtypes. In addition to the palmoplantar distribution seen in other epidermolysis bullosa simplex subtypes, extensive herpetiform blistering spontaneously develops on the trunk and limbs and may lead to scarring or milia formation. The keratin 5 and keratin 14 genes encode proteins that form the primary structural components of the basal epidermal keratinocytes, mutations in either of these genes can cause epidermolysis bullosa simplex. In this study we sequenced these genes in a family with epidermolysis bullosa simplex Dowling-Meara. We report a novel T to C transition in the helix termination peptide of K5 that causes a nonconservative substitution of a highly conserved amino acid within this critical region (I466T). This mutation adds to those previously reported and provides further evidence of phenotype-genotype correlation in epidermolysis bullosa simplex.

摘要

单纯性大疱性表皮松解症Dowling-Meara型(MIM# 1317600)是三种常见的单纯性大疱性表皮松解症亚型中最严重的一种。除了在其他单纯性大疱性表皮松解症亚型中可见的掌跖分布外,躯干和四肢还会自发出现广泛的疱疹样水疱,并可能导致瘢痕形成或粟丘疹形成。角蛋白5和角蛋白14基因编码构成基底表皮角质形成细胞主要结构成分的蛋白质,这两个基因中的任何一个发生突变都可导致单纯性大疱性表皮松解症。在本研究中,我们对一个患有单纯性大疱性表皮松解症Dowling-Meara型的家系中的这些基因进行了测序。我们报告了K5螺旋终止肽中一个新的从T到C的转换,该转换导致这个关键区域内一个高度保守氨基酸的非保守性替代(I466T)。这个突变补充了先前报道的突变,并为单纯性大疱性表皮松解症的表型-基因型相关性提供了进一步的证据。

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