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参与C组着色性干皮病的一个人类DNA修复基因的表达克隆

Expression cloning of a human DNA repair gene involved in xeroderma pigmentosum group C.

作者信息

Legerski R, Peterson C

机构信息

Department of Molecular Genetics, University of Texas, M. D. Anderson Cancer Center, Houston 77030.

出版信息

Nature. 1992 Sep 3;359(6390):70-3. doi: 10.1038/359070a0.

Abstract

Xeroderma pigmentosum (XP) is a rare human autosomal recessive disease characterized by solar sensitivity, high predisposition for developing cancers on areas exposed to sunlight, and, in some cases, neurological abnormalities. XP cells are defective in DNA repair, and complementation of this defect has been used to identify eight genetic groups (A-G and variant). We have developed a simple, highly efficient complementary DNA expression system for use in human cells. Here we use this system to isolate a cDNA clone that restores the ultraviolet sensitivity and unscheduled DNA synthesis of XP-C cells to normal levels. The XP-C complementing clone XPCC encodes a highly hydrophilic protein which is composed of a predicted 823 amino acids and shares limited homology with the product of the yeast DNA repair gene RAD4. The XPCC transcript is undetectable by northern blotting in most XP-C cell lines examined.

摘要

着色性干皮病(XP)是一种罕见的人类常染色体隐性疾病,其特征为对阳光敏感、在暴露于阳光的部位极易患癌,且在某些情况下会出现神经异常。XP细胞的DNA修复存在缺陷,利用这种缺陷的互补作用已鉴定出八个遗传组(A - G组和变异组)。我们开发了一种用于人类细胞的简单、高效的互补DNA表达系统。在此,我们使用该系统分离出一个cDNA克隆,它可将XP - C细胞的紫外线敏感性和非定常DNA合成恢复到正常水平。XP - C互补克隆XPCC编码一种高度亲水的蛋白质,该蛋白质由预测的823个氨基酸组成,与酵母DNA修复基因RAD4的产物具有有限的同源性。在所检测的大多数XP - C细胞系中,通过Northern印迹法无法检测到XPCC转录本。

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