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机械力沿被扫描的双链 DNA 促进 RecA 同源搜索。

RecA homology search is promoted by mechanical stress along the scanned duplex DNA.

机构信息

Department of Physics, Harvard University, Cambridge, MA 02138, USA.

出版信息

Nucleic Acids Res. 2012 Feb;40(4):1717-27. doi: 10.1093/nar/gkr855. Epub 2011 Oct 19.

Abstract

A RecA-single-stranded DNA (RecA-ssDNA) filament searches a genome for sequence homology by rapidly binding and unbinding double-stranded DNA (dsDNA) until homology is found. We demonstrate that pulling on the opposite termini (3' and 5') of one of the two DNA strands in a dsDNA molecule stabilizes the normally unstable binding of that dsDNA to non-homologous RecA-ssDNA filaments, whereas pulling on the two 3', the two 5', or all four termini does not. We propose that the 'outgoing' strand in the dsDNA is extended by strong DNA-protein contacts, whereas the 'complementary' strand is extended by the tension on the base pairs that connect the 'complementary' strand to the 'outgoing' strand. The stress resulting from different levels of tension on its constitutive strands causes rapid dsDNA unbinding unless sufficient homology is present.

摘要

RecA 单链 DNA(RecA-ssDNA)丝通过快速结合和非结合双链 DNA(dsDNA)来搜索基因组中的序列同源性,直到找到同源性。我们证明,拉动 dsDNA 分子中两条 DNA 链之一的相反末端(3'和 5')可以稳定该 dsDNA 与非同源 RecA-ssDNA 丝的通常不稳定的结合,而拉动两个 3'、两个 5'或所有四个末端则不会。我们提出,dsDNA 中的“出链”通过强 DNA-蛋白接触而延伸,而“互补链”通过连接“互补链”和“出链”的碱基对的张力而延伸。由于其组成链上的张力水平不同而产生的应力会导致快速的 dsDNA 非结合,除非存在足够的同源性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d016/3287184/ff5b4b8250aa/gkr855f1.jpg

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