首页> 美国卫生研究院文献>Genetics >Crossing over during Caenorhabditis elegans meiosis requires a conserved MutS-based pathway that is partially dispensable in budding yeast.
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Crossing over during Caenorhabditis elegans meiosis requires a conserved MutS-based pathway that is partially dispensable in budding yeast.

机译:秀丽隐杆线虫减数分裂过程中的杂交需要保守的基于MutS的途径该途径在发芽酵母中部分免除。

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摘要

Formation of crossovers between homologous chromosomes during Caenorhabditis elegans meiosis requires the him-14 gene. Loss of him-14 function severely reduces crossing over, resulting in lack of chiasmata between homologs and consequent missegregation. Cytological analysis showing that homologs are paired and aligned in him-14 pachytene nuclei, together with temperature-shift experiments showing that him-14 functions during the pachytene stage, indicate that him-14 is not needed to establish pairing or synapsis and likely has a more direct role in crossover formation. him-14 encodes a germline-specific member of the MutS family of DNA mismatch repair (MMR) proteins. him-14 has no apparent role in MMR, but like its Saccharomyces cerevisiae ortholog MSH4, has a specialized role in promoting crossing over during meiosis. Despite this conservation, worms and yeast differ significantly in their reliance on this pathway: whereas worms use this pathway to generate most, if not all, crossovers, yeast still form 30-50% of their normal number of crossovers when this pathway is absent. This differential reliance may reflect differential stability of crossover-competent recombination intermediates, or alternatively, the presence of two different pathways for crossover formation in yeast, only one of which predominates during nematode meiosis. We discuss a model in which HIM-14 promotes crossing over by interfering with Holliday junction branch migration.
机译:秀丽隐杆线虫减数分裂过程中同源染色体之间交叉的形成需要him-14基因。 him-14功能的丧失会严重减少交叉,导致同源物之间缺乏视交叉畸形,从而导致错位分离。细胞学分析表明,同源物在him-14粗线烯核中成对排列,并且温度漂移实验表明him-14在粗线蛋白阶段起作用,表明他-14不需要建立配对或突触,并且可能具有在交叉形成中更直接的作用。 him-14编码DNA错配修复(MMR)蛋白MutS家族的种系特异性成员。 him-14在MMR中没有明显的作用,但是像它的酿酒酵母直系同源物MSH4一样,在促进减数分裂过程中的交叉方面具有特殊作用。尽管有这种保守性,蠕虫和酵母在对这种途径的依赖性上却有很大不同:蠕虫使用这种途径来产生大部分(即使不是全部)交换,但如果没有这种途径,酵母仍会形成其正常交换次数的30-50%。这种不同的依赖性可能反映了具有交叉能力的重组中间体的不同稳定性,或者反映了酵母中两种不同的交叉形成途径的存在,其中只有一种在线虫减数分裂中占主导。我们讨论了一种模型,其中HIM-14通过干扰霍利迪交界处分支迁移来促进交叉。

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