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Sororin loads to the synaptonemal complex central region independently of meiotic cohesin complexes

机译:索罗林独立于减数分裂粘附素复合物加载到突触中央复合体中央区域

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摘要

The distribution and regulation of the cohesin complexes have been extensively studied during mitosis. However, the dynamics of their different regulators in vertebrate meiosis is largely unknown. In this work, we have analyzed the distribution of the regulatory factor Sororin during male mouse meiosis. Sororin is detected at the central region of the synaptonemal complex during prophase I, in contrast with the previously reported localization of other cohesin components in the lateral elements. This localization of Sororin depends on the transverse filaments protein SYCP1, but not on meiosis‐specific cohesin subunits REC8 and SMC1β. By late prophase I, Sororin accumulates at centromeres and remains there up to anaphase II. The phosphatase activity of PP2A seems to be required for this accumulation. We hypothesize that Sororin function at the central region of the synaptonemal complex could be independent on meiotic cohesin complexes. In addition, we suggest that Sororin participates in the regulation of centromeric cohesion during meiosis in collaboration with SGO2‐PP2A.
机译:在有丝分裂期间已经广泛研究了粘着蛋白复合物的分布和调节。但是,它们在脊椎动物减数分裂中不同调控因子的动力学很大程度上是未知的。在这项工作中,我们分析了雄性小鼠减数分裂过程中调节因子Sororin的分布。与之前报道的其他黏着蛋白成分在侧向元件中的定位相反,在前期I期间,在突触复合体的中央区域检测到了索罗林。 Sororin的这种定位取决于横向丝蛋白SYCP1,而不取决于减数分裂特异性粘附素亚基REC8和SMC1β。在第一阶段晚期之前,索罗林在着丝粒处积累,一直保持到第二阶段后期。 PP2A的磷酸酶活性似乎是这种积累所必需的。我们假设Sororin在突触复合物的中央区域的功能可能独立于减数分裂粘附素复合物。此外,我们建议Sororin与SGO2-PP2A一起参与减数分裂过程中着丝粒内聚力的调节。

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