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大肠杆菌解旋酶II(UvrD)蛋白在切口和平端处启动DNA解旋。

Escherichia coli helicase II (UvrD) protein initiates DNA unwinding at nicks and blunt ends.

作者信息

Runyon G T, Bear D G, Lohman T M

机构信息

Department of Biochemistry and Biophysics, Texas A&M University, College Station 77843-2128.

出版信息

Proc Natl Acad Sci U S A. 1990 Aug;87(16):6383-7. doi: 10.1073/pnas.87.16.6383.

Abstract

The Escherichia coli uvrD gene product, helicase II, is required for both methyl-directed mismatch and uvrABC excision repair and is believed to function by unwinding duplex DNA. Initiation of unwinding may occur specifically at either a mismatch or a nick, although no direct evidence for this has previously been reported. It has recently been shown that helicase II can unwind fully duplex linear and nicked circular DNA with lengths of at least approximately 2700 base pairs in vitro; hence, a flanking region of single-stranded DNA is not required to initiate DNA unwinding. In studies with uniquely nicked duplex DNA, we present EM evidence that helicase II protein initiates DNA unwinding at the nick, with unwinding proceeding bidirectionally. We also show that helicase II protein initiates DNA unwinding at the blunt ends of linear DNA, rather than in internal regions. These data provide direct evidence that helicase II protein can initiate unwinding of duplex DNA at a nick, in the absence of auxiliary proteins. We propose that helicase II may initiate unwinding from a nick in a number of DNA repair processes.

摘要

大肠杆菌uvrD基因产物解旋酶II是甲基导向错配修复和uvrABC切除修复所必需的,据信它通过解开双链DNA发挥作用。解旋起始可能特异性地发生在错配或切口处,尽管此前尚无直接证据报道。最近有研究表明,解旋酶II在体外能够解开长度至少约为2700个碱基对的完全双链线性和带切口的环状DNA;因此,起始DNA解旋并不需要单链DNA侧翼区域。在对独特切口的双链DNA的研究中,我们提供了电子显微镜证据,表明解旋酶II蛋白在切口处起始DNA解旋,并双向进行。我们还表明,解旋酶II蛋白在线性DNA的平端起始DNA解旋,而不是在内部区域。这些数据提供了直接证据,表明在没有辅助蛋白的情况下,解旋酶II蛋白能够在切口处起始双链DNA解旋。我们提出,解旋酶II可能在许多DNA修复过程中从切口处起始解旋。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cc49/54538/067a98da37a7/pnas01041-0385-a.jpg

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