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首页> 外文期刊>Nature Communications >The Escherichia coli Tus-Ter replication fork barrier causes site-specific DNA replication perturbation in yeast
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The Escherichia coli Tus-Ter replication fork barrier causes site-specific DNA replication perturbation in yeast

机译:大肠杆菌Tus-Ter复制叉屏障会导致酵母中的特定位点DNA复制扰动

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摘要

Replication fork (RF) pausing occurs at both ` programmed' sites and non-physiological barriers (for example, DNA adducts). Programmed RF pausing is required for site-specific DNA replication termination in Escherichia coli, and this process requires the binding of the polar terminator protein, Tus, to specific DNA sequences called Ter. Here, we demonstrate that Tus-Ter modules also induce polar RF pausing when engineered into the Saccharomyces cerevisiae genome. This heterologous RF barrier is distinct from a number of previously characterized, protein-mediated, RF pause sites in yeast, as it is neither Tof1-dependent nor counteracted by the Rrm3 helicase. Although the yeast replisome can overcome RF pausing at Tus-Ter modules, this event triggers site-specific homologous recombination that requires the RecQ helicase, Sgs1, for its timely resolution. We propose that Tus-Ter can be utilized as a versatile, site-specific, heterologous DNA replication-perturbing system, with a variety of potential applications.
机译:复制叉(RF)暂停发生在“程序化”位置和非生理性障碍(例如DNA加合物)上。大肠杆菌中特定位置的DNA复制终止需要程序化的RF暂停,并且此过程需要将极性终止子蛋白Tus与称为Ter的特定DNA序列结合。在这里,我们证明了当工程改造成酿酒酵母基因组时,Tus-Ter模块也能诱导极性RF暂停。此异源RF屏障与酵母中许多先前表征的蛋白质介导的RF暂停位点不同,因为它既不依赖于Tof1也不被Rrm3解旋酶抵消。尽管酵母复制体可以克服Tus-Ter模块的RF暂停,但此事件会触发特定于位点的同源重组,这需要RecQ解旋酶Sgs1才能及时解决。我们建议Tus-Ter可以用作通用的,特定于位点的异源DNA复制干扰系统,具有多种潜在应用。

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