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The cohesin release factor Wapl interacts with Bub3 to govern SAC activity in female meiosis I

机译:Cohesin释放因子WAPL与Bub3相互作用,治理女性减数分裂中的囊活性

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During mitotic prophase, cohesins are removed from chromosome arms by Wapl to ensure faithful sister chromatid separation. However, during female meiosis I, the resolution of chiasmata requires the proteolytic cleavage of cohesin subunit Rec8 along chromosome arms by Separase to separate homologs, and thus the role of Wapl remained unknown. Here, we report that Wapl functions as a regulator of spindle assembly checkpoint (SAC) to prevent aneuploidy in meiosis I. Depletion of Wapl accelerates meiotic progression, inactivates SAC, and causes meiotic defects such as aberrant spindle/chromosome structure and incorrect kinetochore-microtubule (K-MT) attachment, consequently leading to aneuploid eggs. Notably, we identify Bub3 as a binding partner of Wapl by immunoprecipitation and mass spectrometry analysis. We further determine that Wapl controls the SAC activity by maintaining Bub3 protein level and document that exogenous Bub3 restores the normal meiosis in Wapl-depleted oocytes. Together, our findings uncover unique, noncanonical roles for Wapl in mediating control of the SAC in female meiosis I.
机译:在有丝分裂预防期间,通过WAPL从染色体臂中除去辅酶,以确保忠实的姐妹染色体分离。然而,在雌性减数分裂I期间,Chiasmata的分辨率要求沿着分离的同源物沿染色体臂沿染色体臂的蛋白质亚基REC8的蛋白水解切割,因此WAPL的作用仍然未知。在这里,我们将WAPL用作主轴组件检查点(SAC)的调节器,以防止减数分裂中的短倍性I. WAPL的耗尽加速了减少人的进展,灭活囊,并导致诸如异常主轴/染色体结构等减肥缺陷和不正确的Kinetochore-Microtubule。 (K-MT)附着,因此导致空腹卵。值得注意的是,通过免疫沉淀和质谱分析,我们将Bub3鉴定为WAPL的结合伴侣。我们进一步确定WAPL通过维持Bub3蛋白质水平和文献,即外源Bub3在WAPL耗尽的卵母细胞中恢复正常的MeIsis。我们的研究结果在一起揭示了WAPL的独特,非甘露糖作用在雌性减数分裂中的囊中的控制中。

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