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酵母Rad1蛋白对霍利迪连接体的切割

Holliday junction cleavage by yeast Rad1 protein.

作者信息

Habraken Y, Sung P, Prakash L, Prakash S

机构信息

Sealy Center for Molecular Science, University of Texas Medical Branch, Galveston 77555-1061.

出版信息

Nature. 1994 Oct 6;371(6497):531-4. doi: 10.1038/371531a0.

Abstract

In Saccharomyces cerevisiae, of the many genes required for excision repair of ultraviolet-damaged DNA, only RAD1 and RAD10 also function in genetic recombination. Complex formation between the RAD1 and RAD10 gene products activates an endonucleolytic function that nicks single-stranded DNA and negatively supercoiled double-stranded DNA. To characterize the recombination role of the proteins Rad1 and Rad10, we have investigated their interaction with the Holliday junction, a four-stranded structure that results from single-stranded crossover between two duplex DNA molecules and whose resolution is obligatory for the generation of mature recombinants. We show that Rad1 binds specifically to a Holliday junction and, in the presence of magnesium, catalyses the endonucleolytic cleavage of the junction. Junction cleavage by Rad1 proceeds sufficiently without Rad10, thus identifying Rad1 as the catalytic subunit of Rad1/Rad10 endonuclease.

摘要

在酿酒酵母中,众多参与紫外线损伤DNA切除修复所需的基因里,只有RAD1和RAD10也在基因重组中发挥作用。RAD1和RAD10基因产物之间形成的复合物激活了一种核酸内切酶功能,该功能能切割单链DNA和负超螺旋双链DNA。为了表征Rad1和Rad10蛋白在重组中的作用,我们研究了它们与霍利迪连接体的相互作用,霍利迪连接体是一种四链结构,由两个双链DNA分子之间的单链交叉产生,其拆分对于产生成熟重组体来说是必不可少的。我们发现Rad1能特异性结合霍利迪连接体,并且在镁存在的情况下,催化连接体的核酸内切酶切割。在没有Rad10的情况下,Rad1对连接体的切割也能充分进行,从而确定Rad1是Rad1/Rad10核酸内切酶的催化亚基。

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