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Complete kinetochore tracking reveals error-prone homologous chromosome biorientation in mammalian oocytes

机译:完整的线粒体追踪揭示了哺乳动物卵母细胞中容易出错的同源染色体生物取向

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Chromosomes must establish stable biorientation prior to anaphase to achieve faithful segregation during cell division. The detailed process by which chromosomes are bioriented and how biorientation is coordinated with spindle assembly and chromosome congression remain unclear. Here, we provide complete 3D kinetochore-tracking datasets throughout cell division by high-resolution imaging of meiosis I in live mouse oocytes. We show that in acentrosomal oocytes, chromosome congression forms an intermediate chromosome configuration, the prometaphase belt, which precedes biorientation. Chromosomes then invade the elongating spindle center to form the metaphase plate and start biorienting. Close to 90% of all chromosomes undergo one or more rounds of error correction of their kinetochore-microtubule attachments before achieving correct biorientation. This process depends on Aurora kinase activity. Our analysis reveals the error-prone nature of homologous chromosome biorientation, providing a possible explanation for the high incidence of aneuploid eggs observed in mammals, including humans.
机译:染色体必须在后期之前建立稳定的生物取向,以在细胞分裂过程中实现忠实的分离。染色体双向定向的详细过程以及生物定向与纺锤体装配和染色体国会如何协调的详细过程仍不清楚。在这里,我们通过活体小鼠卵母细胞中减数分裂I的高分辨率成像,提供了整个细胞分裂过程中完整的3D线粒体追踪数据集。我们表明,在无人染色体的卵母细胞中,染色体国会形成了一个中间的染色体构型,即前生相带,它位于生物定向之前。然后,染色体侵入伸长的纺锤中心,形成中期板并开始生物定向。在实现正确的生物定向之前,将近90%的所有染色体都要经过一轮或多轮其动线体-微管附件的错误校正。该过程取决于极光激酶活性。我们的分析揭示了同源染色体生物定向的容易出错的性质,为在包括人在内的哺乳动物中观察到的非整倍体蛋的高发病率提供了可能的解释。

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