首页> 外文期刊>Genetics: A Periodical Record of Investigations Bearing on Heredity and Variation >CYS3, a Hotspot of Meiotic Recombination in Saccharomyces cerevisiae: Effects of Heterozygosity and Mismatch Repair Functions on Gene Conversion and Recombination Intermediates
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CYS3, a Hotspot of Meiotic Recombination in Saccharomyces cerevisiae: Effects of Heterozygosity and Mismatch Repair Functions on Gene Conversion and Recombination Intermediates

机译:CYS3,在酿酒酵母中减数分裂重组的热点:杂合性和错配修复功能对基因转换和重组中间产物的影响。

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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.
机译:我们已经检查了CYS3位点的减数分裂重组。遗传分析表明,CYS3是减数分裂基因转化的热点,推测转化频率为5'–3'极性梯度。在存在msh2和pms1突变的情况下,此梯度得以缓解,这表明减数分裂重组中涉及错配修复功能。为了研究错配修复蛋白在减数分裂重组中的作用,我们对存在或不存在CYS3等位基因差异的野生型和msh2 pms1菌株中的减数分裂DNA进行了物理分析。 CYS3中的突变或失配修复功能的缺失都不会影响附近的重组起始DNA双链断裂(DSB)的频率和分布。在msh2 pms1和野生型菌株中,DSB的加工也相似。我们得出的结论是,错配修复功能在启动步骤不控制减数分裂基因转化事件的分布。在MSH2 PMS1背景中,CYS3中用于移码突变的异源等位基因菌株的基因转化频率高于单独观察到的任一标记。物理分析表明,DSB的形成没有任何改变,表明该标志物效应是由尚未被理解的后续加工事件引起的。

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