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酵母RAD14基因和人类A型着色性干皮病DNA修复基因编码同源蛋白。

Yeast RAD14 and human xeroderma pigmentosum group A DNA-repair genes encode homologous proteins.

作者信息

Bankmann M, Prakash L, Prakash S

机构信息

Department of Biophysics, University of Rochester School of Medicine, New York 14642-8408.

出版信息

Nature. 1992 Feb 6;355(6360):555-8. doi: 10.1038/355555a0.

Abstract

Xeroderma pigmentosum (XP), a human autosomal recessive disorder, is characterized by extreme sensitivity to sunlight and high incidence of skin cancers. XP cells are defective in the incision step of excision repair of DNA damaged by ultraviolet light. Cell fusion studies have defined seven XP complementation groups, XP-A to XP-G. Similar genetic complexity of excision repair is observed in the yeast Saccharomyces cerevisiae. Mutations in any one of five yeast genes, RAD1, RAD2, RAD3, RAD4, and RAD10, cause a total defect in incision and an extreme sensitivity to ultraviolet light. Here we report the characterization of the yeast RAD14 gene. The available rad14 point mutant is only moderately ultraviolet-sensitive, and it performs a substantial amount of incision of damaged DNA. Our studies with the rad14 deletion (delta) mutation indicate an absolute requirement of RAD14 in incision. RAD14 encodes a highly hydrophilic protein of 247 amino acids containing zinc-finger motifs, and it is similar to the protein encoded by the human XPAC gene that complements XP group A cell lines.

摘要

着色性干皮病(XP)是一种人类常染色体隐性疾病,其特征为对阳光极度敏感且皮肤癌发病率高。XP细胞在紫外线损伤DNA的切除修复的切口步骤中存在缺陷。细胞融合研究确定了七个XP互补组,即XP-A至XP-G。在酿酒酵母中也观察到切除修复具有类似的遗传复杂性。酿酒酵母五个基因RAD1、RAD2、RAD3、RAD4和RAD10中任何一个发生突变,都会导致切口完全缺陷并对紫外线极度敏感。在此我们报告酵母RAD14基因的特征。现有的rad14点突变体仅对紫外线中度敏感,并且它能对受损DNA进行大量的切口操作。我们对rad14缺失(delta)突变的研究表明,切口过程中绝对需要RAD14。RAD14编码一个含有247个氨基酸的高度亲水性蛋白,该蛋白含有锌指基序,并且它与人XPAC基因编码的蛋白相似,后者可互补XP A组细胞系。

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