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酿酒酵母“易出错”修复组突变体之间的遗传相互作用及其对重组和诱变的影响。

Genetic interactions between mutants of the 'error-prone' repair group of Saccharomyces cerevisiae and their effect on recombination and mutagenesis.

作者信息

Liefshitz B, Steinlauf R, Friedl A, Eckardt-Schupp F, Kupiec M

机构信息

Department of Molecular Microbiology and Biotechnology, Tel Aviv University, Israel.

出版信息

Mutat Res. 1998 Mar;407(2):135-45. doi: 10.1016/s0921-8777(97)00070-0.

Abstract

We have created an isogenic series of yeast strains that carry genetic systems to monitor different types of recombination and mutation [B. Liefshitz, A. Parket, R. Maya, M. Kupiec, The role of DNA repair genes in recombination between repeated sequences in yeast, Genetics 140 (1995) 1199-1211.]. In the present study we characterize the effect of mutations in genes of the 'error-prone' or postreplicative repair group on recombination and mutation. We show that rad5 and rad18 strains have elevated levels of spontaneous recombination, both of ectopic gene conversion and of recombination between direct repeats. The increase in recombination levels is similar in both mutants and in the rad5 rad18 double mutant, suggesting that the RAD5 and RAD18 gene products act together with respect to spontaneous recombination. In contrast, RAD5 and RAD18 play alternative roles in mutagenic repair: mutations in each of these genes elevate spontaneous forward mutation at the CAN1 locus, but when both genes are deleted, a low level of spontaneous mutagenesis is seen. The RAD5/RAD18 pathway of mutagenic repair is dependent on the REV3-encoded translesion polymerase. We analyze the interactions between the RAD5 and RAD18 gene products and other repair genes. The high recombination levels seen in rad5 and rad18 mutants is dependent on the RAD1, RAD51, RAD52, and RAD57 genes. The Srs2 helicase plays an important role in creating the recombinogenic substrate(s) processed by the RAD5 and RAD18 gene products.

摘要

我们构建了一系列同基因酵母菌株,这些菌株带有用于监测不同类型重组和突变的遗传系统[B. 利夫希茨、A. 帕克特、R. 玛雅、M. 库皮克,《酵母中DNA修复基因在重复序列间重组中的作用》,《遗传学》140卷(1995年)第1199 - 1211页]。在本研究中,我们表征了“易出错”或复制后修复组基因中的突变对重组和突变的影响。我们发现,rad5和rad18菌株的自发重组水平升高,包括异位基因转换和直接重复序列间的重组。两个突变体以及rad5 rad18双突变体的重组水平升高情况相似,这表明RAD5和RAD18基因产物在自发重组方面共同发挥作用。相比之下,RAD5和RAD18在诱变修复中发挥不同作用:这些基因中的每一个发生突变都会提高CAN1位点的自发正向突变率,但当两个基因都缺失时,自发诱变水平较低。诱变修复的RAD5/RAD18途径依赖于REV3编码的跨损伤聚合酶。我们分析了RAD5和RAD18基因产物与其他修复基因之间的相互作用。在rad5和rad18突变体中观察到的高重组水平依赖于RAD1、RAD51、RAD52和RAD57基因。Srs2解旋酶在产生由RAD5和RAD18基因产物处理的重组底物方面起重要作用。

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