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首页> 外文期刊>PLoS Genetics >A Yeast Two-Hybrid Screen for SYP-3 Interactors Identifies SYP-4, a Component Required for Synaptonemal Complex Assembly and Chiasma Formation in Caenorhabditis elegans Meiosis
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A Yeast Two-Hybrid Screen for SYP-3 Interactors Identifies SYP-4, a Component Required for Synaptonemal Complex Assembly and Chiasma Formation in Caenorhabditis elegans Meiosis

机译:酵母SYP-3相互作用物的两杂交筛选可鉴定SYP-4,这是秀丽隐杆线虫减数分裂中突触复合体装配和Chi裂形成所必需的组件。

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The proper assembly of the synaptonemal complex (SC) between homologs is critical to ensure accurate meiotic chromosome segregation. The SC is a meiotic tripartite structure present from yeast to humans, comprised of proteins assembled along the axes of the chromosomes and central region (CR) proteins that bridge the two chromosome axes. Here we identify SYP-4 as a novel structural component of the SC in Caenorhabditis elegans. SYP-4 interacts in a yeast two-hybrid assay with SYP-3, one of components of the CR of the SC, and is localized at the interface between homologs during meiosis. SYP-4 is essential for the localization of SYP-1, SYP-2, and SYP-3 CR proteins onto chromosomes, thereby playing a crucial role in the stabilization of pairing interactions between homologous chromosomes. In the absence of SYP-4, the levels of recombination intermediates, as indicated by RAD-51 foci, are elevated in mid-prophase nuclei, and crossover recombination events are significantly reduced. The lack of chiasmata observed in syp-4 mutants supports the elevated levels of chromosome nondisjunction manifested in high embryonic lethality. Altogether our findings place SYP-4 as a central player in SC formation and broaden our understanding of the structure of the SC and its assembly.
机译:同源物之间的突触复合物(SC)的正确组装对于确保准确的减数分裂染色体分离至关重要。 SC是从酵母到人类的减数分裂三方结构,由沿染色体轴组装的蛋白质和桥接两个染色体轴的中央区域(CR)蛋白质组成。在这里,我们确定SYP-4为秀丽隐杆线虫中SC的新型结构成分。 SYP-4在酵母双杂交检测中与SYP-3(SC的CR的成分之一)相互作用,并在减数分裂过程中位于同源物之间的界面上。 SYP-4对于SYP-1,SYP-2和SYP-3 CR蛋白在染色体上的定位至关重要,因此在稳定同源染色体之间的配对相互作用中起着至关重要的作用。在缺少SYP-4的情况下,如RAD-51病灶所示,重组中间体的水平在前中期细胞核中升高,并且交叉重组事件显着减少。在syp-4突变体中观察到的缺乏散光性支持了高胚胎致死率中染色体非分离性水平的升高。总之,我们的发现使SYP-4成为SC形成的中心力量,并拓宽了我们对SC结构及其装配的理解。

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