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CYS3,酿酒酵母减数分裂重组的一个热点。杂合性和错配修复功能对基因转换和重组中间体的影响。

CYS3, a hotspot of meiotic recombination in Saccharomyces cerevisiae. Effects of heterozygosity and mismatch repair functions on gene conversion and recombination intermediates.

作者信息

Vedel M, Nicolas A

机构信息

Institut Curie, Section de Recherche, Compartimentation et Dynamique Cellulaires, UMR144, Centre National de la Recherche Scientifique, 75248 Paris Cedex 05, France.

出版信息

Genetics. 1999 Apr;151(4):1245-59. doi: 10.1093/genetics/151.4.1245.

Abstract

We have examined meiotic recombination at the CYS3 locus. Genetic analysis indicates that CYS3 is a hotspot of meiotic gene conversion, with a putative 5'-3' polarity gradient of conversion frequencies. This gradient is relieved in the presence of msh2 and pms1 mutations, indicating an involvement of mismatch repair functions in meiotic recombination. To investigate the role of mismatch repair proteins in meiotic recombination, we performed a physical analysis of meiotic DNA in wild-type and msh2 pms1 strains in the presence or absence of allelic differences at CYS3. Neither the mutations in CYS3 nor the absence of mismatch repair functions affects the frequency and distribution of nearby recombination-initiating DNA double-strand breaks (DSBs). Processing of DSBs is also similar in msh2 pms1 and wild-type strains. We conclude that mismatch repair functions do not control the distribution of meiotic gene conversion events at the initiating steps. In the MSH2 PMS1 background, strains heteroallelic for frameshift mutations in CYS3 exhibit a frequency of gene conversion greater than that observed for either marker alone. Physical analysis revealed no modification in the formation of DSBs, suggesting that this marker effect results from subsequent processing events that are not yet understood.

摘要

我们检测了CYS3位点的减数分裂重组。遗传分析表明,CYS3是减数分裂基因转换的热点,具有假定的5'-3'转换频率极性梯度。在存在msh2和pms1突变的情况下,这种梯度消失,表明错配修复功能参与了减数分裂重组。为了研究错配修复蛋白在减数分裂重组中的作用,我们在CYS3存在或不存在等位基因差异的情况下,对野生型和msh2 pms1菌株的减数分裂DNA进行了物理分析。CYS3中的突变以及错配修复功能的缺失均不影响附近重组起始DNA双链断裂(DSB)的频率和分布。在msh2 pms1和野生型菌株中,DSB的处理也相似。我们得出结论,错配修复功能在起始步骤中并不控制减数分裂基因转换事件的分布。在MSH2 PMS1背景下,CYS3中移码突变的杂合等位基因菌株表现出的基因转换频率高于单独观察到的任何一个标记的频率。物理分析表明DSB的形成没有改变,这表明这种标记效应是由尚未了解的后续处理事件导致的。

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