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人类75千道尔顿DNA配对蛋白与原癌蛋白TLS/FUS相同,且能够促进D环形成。

Human 75-kDa DNA-pairing protein is identical to the pro-oncoprotein TLS/FUS and is able to promote D-loop formation.

作者信息

Baechtold H, Kuroda M, Sok J, Ron D, Lopez B S, Akhmedov A T

机构信息

Basel Institute for Immunology, Grenzacherstrasse 487, CH-4005 Basel, Switzerland.

出版信息

J Biol Chem. 1999 Nov 26;274(48):34337-42. doi: 10.1074/jbc.274.48.34337.

Abstract

Homologous recombination plays a fundamental role in DNA double-strand break repair. Previously, we detected two mammalian nuclear proteins of 100 and 75 kDa (POMp100 and POMp75, respectively) that are able to promote homologous DNA pairing, a key step in homologous recombination. Here we describe the identification of human (h) POMp75 as the pro-oncoprotein TLS/FUS. hPOMp75/TLS binds both single- and double-stranded DNAs and mediates annealing of complementary DNA strands. More important, it promotes the uptake of a single-stranded oligonucleotide into a homologous superhelical DNA to form a D-loop. The formation of a D-loop is an essential step in DNA double-strand break repair through recombination. DNA annealing and D-loop formation catalyzed by hPOMp75/TLS require Mg(2+) and are ATP-independent. Interestingly, the oncogenic fusion form TLS-CHOP is not able to promote DNA pairing. These data suggest a possible role for hPOMp75/TLS in maintenance of genomic integrity.

摘要

同源重组在DNA双链断裂修复中起着基础性作用。此前,我们检测到两种分子量分别为100 kDa和75 kDa的哺乳动物核蛋白(分别为POMp100和POMp75),它们能够促进同源DNA配对,这是同源重组中的关键步骤。在此,我们描述了人类(h)POMp75被鉴定为原癌蛋白TLS/FUS。hPOMp75/TLS既能结合单链DNA,也能结合双链DNA,并介导互补DNA链的退火。更重要的是,它能促进单链寡核苷酸进入同源超螺旋DNA以形成D环。D环的形成是通过重组进行DNA双链断裂修复的关键步骤。由hPOMp75/TLS催化的DNA退火和D环形成需要Mg(2+)且不依赖ATP。有趣的是,致癌融合形式TLS-CHOP无法促进DNA配对。这些数据表明hPOMp75/TLS在维持基因组完整性方面可能发挥作用。

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