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Separase is required for homolog and sister disjunction during drosophila melanogaster male meiosis, but not for biorientation of sister centromeres

机译:果蝇雄性减数分裂过程中同系物和姊妹分离需要分离酶,但姊妹着丝粒的生物定向则不需要

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摘要

Spatially controlled release of sister chromatid cohesion during progression through the meiotic divisions is of paramount importance for error-free chromosome segregation during meiosis. Cohesion is mediated by the cohesin protein complex and cleavage of one of its subunits by the endoprotease separase removes cohesin first from chromosome arms during exit from meiosis I and later from the pericentromeric region during exit from meiosis II. At the onset of the meiotic divisions, cohesin has also been proposed to be present within the centromeric region for the unification of sister centromeres into a single functional entity, allowing bipolar orientation of paired homologs within the meiosis I spindle. Separase-mediated removal of centromeric cohesin during exit from meiosis I might explain sister centromere individualization which is essential for subsequent biorientation of sister centromeres during meiosis II. To characterize a potential involvement of separase in sister centromere individualization before meiosis II, we have studied meiosis in Drosophila melanogaster males where homologs are not paired in the canonical manner. Meiosis does not include meiotic recombination and synaptonemal complex formation in these males. Instead, an alternative homolog conjunction system keeps homologous chromosomes in pairs. Using independent strategies for spermatocyte-specific depletion of separase complex subunits in combination with time-lapse imaging, we demonstrate that separase is required for the inactivation of this alternative conjunction at anaphase I onset. Mutations that abolish alternative homolog conjunction therefore result in random segregation of univalents during meiosis I also after separase depletion. Interestingly, these univalents become bioriented during meiosis II, suggesting that sister centromere individualization before meiosis II does not require separase.
机译:在通过减数分裂分裂过程中,姐妹染色单体凝聚力的空间控制释放对于减数分裂过程中无错染色体的分离至关重要。凝聚力是由凝聚素蛋白复合物介导的,内切蛋白酶分离酶切割它的一个亚基会在减数分裂I退出时首先从染色体臂上去除凝聚素,然后在减数分裂II退出时从着丝粒区域去除。在减数分裂分裂开始时,还提出了粘附蛋白存在于着丝粒区域内,以将姊妹着丝粒统一为单个功能实体,从而使成对的同源物在减数分裂I纺锤体内双极性取向。减数分裂退出过程中分离酶介导的着丝粒粘着蛋白的去除I可能解释了姊妹着丝粒的个体化,这对于继代减数分裂II期间姊妹着丝粒的后续生物定向至关重要。为了表征分离酶可能在减数分裂II之前的姊妹着丝粒个体化中的作用,我们研究了果蝇黑腹果蝇雄性的减数分裂,其中同源物未以标准方式配对。在这些男性中,减数分裂不包括减数分裂重组和突触复合体的形成。取而代之的是,另一种同源联结系统使同源染色体成对存在。使用独立的策略与延时成像相结合的分离酶复杂亚基的精母细胞特异性耗竭,我们证明分离酶是在后期I发作时使这种替代结合失活所必需的。因此,在分离酶耗竭后,在减数分裂I期间,废除替代同源连体的突变也会导致单价的随机分离。有趣的是,这些单价在减数分裂II期间变成双向的,这表明减数分裂II之前的姊妹着丝粒个性化不需要分离酶。

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