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一种与植物蓝光受体相似的人类光裂合酶同源物的克隆、组织表达及定位

Cloning, tissue expression, and mapping of a human photolyase homolog with similarity to plant blue-light receptors.

作者信息

van der Spek P J, Kobayashi K, Bootsma D, Takao M, Eker A P, Yasui A

机构信息

Department of Cell Biology and Genetics, Erasmus University Rotterdam, The Netherlands.

出版信息

Genomics. 1996 Oct 15;37(2):177-82. doi: 10.1006/geno.1996.0539.

Abstract

Enzymatic photoreactivation is a DNA repair mechanism that removes UV-induced pyrimidine dimer lesions by action of a single enzyme, photolyase, and visible light. Its presence has been demonstrated in a wide variety of organisms, ranging from simple prokaryotes to higher eukaryotes. We have isolated a human gene encoding a 66-kDa protein that shows clear overall homology to known bacterial photolyase genes. The human gene product is more similar to plant blue-light receptors within class I photolyases than to higher eukaryote class II photolyases. Northern blot analysis showed two transcripts with constitutive expression in all tissues examined and an elevated expression in testis. In situ hybridization with a cDNA-derived probe localized this human gene to chromosome 12q23-q24.1. Southern analysis of the cloned human gene suggests a wide distribution of the gene family in various species.

摘要

酶促光复活是一种DNA修复机制,它通过单一酶(光解酶)和可见光的作用去除紫外线诱导的嘧啶二聚体损伤。从简单的原核生物到高等真核生物,在各种各样的生物体中都已证实其存在。我们分离出了一个编码66 kDa蛋白的人类基因,该蛋白与已知的细菌光解酶基因显示出明显的整体同源性。与I类光解酶中的高等真核生物II类光解酶相比,人类基因产物与植物蓝光受体更为相似。Northern印迹分析显示,在所检测的所有组织中均有两种组成型表达的转录本,且在睾丸中表达升高。用cDNA衍生探针进行原位杂交将该人类基因定位到12q23-q24.1染色体上。对克隆的人类基因进行Southern分析表明该基因家族在各种物种中分布广泛。

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