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首页> 外文期刊>Genes and Development: a Journal Devoted to the Molecular Analysis of Gene Expression in Eukaryotes, Prokaryotes, and Viruses >The fission yeast meiosis-specific Dmc1 recombinase mediates formation and branch migration of Holliday junctions by preferentially promoting strand exchange in a direction opposite to that of Rad51.
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The fission yeast meiosis-specific Dmc1 recombinase mediates formation and branch migration of Holliday junctions by preferentially promoting strand exchange in a direction opposite to that of Rad51.

机译:裂变酵母减数分裂特异性Dmc1重组酶通过优先促进与Rad51方向相反的链交换来介导霍利迪结的形成和分支迁移。

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摘要

Homologous recombination proceeds via the formation of several intermediates including Holliday junctions (HJs), which are important for creating crossover products. DNA strand exchange is a core reaction that produces these intermediates that is directly catalyzed by RecA family recombinases, of which there are two types in eukaryotes: universal Rad51 and meiosis-specific Dmc1. We demonstrated previously that Rad51 promotes four-strand exchange, mimicking the formation and branch migration of HJs. Here we show that Dmc1 from fission yeast has a similar activity, which requires ATP hydrolysis and is independent of an absolute requirement for the Swi5-Sfr1 complex. These features are critically different from three-strand exchange mediated by Dmc1, but similar to those of four-strand exchange mediated by Rad51, suggesting that strand exchange reactions between duplex-duplex and single-duplex DNAs are mechanistically different. Interestingly, despite similarities in protein structure and in reaction features, the preferential polarities of Dmc1 and Rad51 strand exchange are different (Dmc1 promotes exchange in the 5'-to-3' direction and Rad51 promotes exchange in the 3'-to-5' direction relative to the ssDNA region of the DNA substrate). The significance of the Dmc1 polarity is discussed within the context of the necessity for crossover production.
机译:同源重组通过包括霍利迪结(HJ)在内的几种中间体的形成而进行,这对于产生交叉产物很重要。 DNA链交换是产生这些中间体的核心反应,这些中间体直接由RecA家族重组酶催化,在真核生物中有两种类型:通用Rad51和减数分裂特异性Dmc1。我们以前证明Rad51促进四链交换,模仿HJ的形成和分支迁移。在这里,我们显示裂变酵母的Dmc1具有相似的活性,需要ATP水解,并且与Swi5-Sfr1复合物的绝对要求无关。这些特征与Dmc1介导的三链交换极为不同,但与Rad51介导的四链交换的特征相似,这表明双链双链DNA与单双链DNA之间的链交换反应在机理上有所不同。有趣的是,尽管蛋白质结构和反应特征相似,但Dmc1和Rad51链交换的优先极性不同(Dmc1促进5'至3'方向的交换,Rad51促进3'至5'的交换。相对于DNA底物的ssDNA区域的方向)。在交叉生产的必要性背景下,讨论了Dmc1极性的重要性。

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