Department of Cell and Molecular Biology, Karolinska Institutet, Stockholm, Sweden.
Laboratory for Chromosome Segregation, RIKEN Center for Biosystems Dynamics Research, Kobe, Japan.
EMBO Rep. 2019 Aug;20(8):e47905. doi: 10.15252/embr.201947905. Epub 2019 Jul 10.
The accuracy of the two sequential meiotic divisions in oocytes is essential for creating a haploid gamete with a normal chromosomal content. Here, we have analysed the 3D dynamics of chromosomes during the second meiotic division in live mouse oocytes. We find that chromosomes form stable kinetochore-microtubule attachments at the end of prometaphase II stage that are retained until anaphase II onset. Remarkably, we observe that more than 20% of the kinetochore-microtubule attachments at the metaphase II stage are merotelic or lateral. However, < 1% of all chromosomes at onset of anaphase II are found to lag at the spindle equator and < 10% of the laggards missegregate and give rise to aneuploid gametes. Our results demonstrate that aberrant kinetochore-microtubule attachments are not corrected at the metaphase stage of the second meiotic division. Thus, the accuracy of the chromosome segregation process in mouse oocytes during meiosis II is ensured by an efficient correction process acting at the anaphase stage.
两个连续减数分裂过程在卵母细胞中的准确性对于产生具有正常染色体含量的单倍体配子至关重要。在这里,我们分析了活鼠卵母细胞中第二次减数分裂过程中染色体的 3D 动力学。我们发现染色体在中期 II 阶段末期形成稳定的动粒-微管连接,这些连接一直保留到后期 II 开始。值得注意的是,我们观察到超过 20%的中期 II 阶段的动粒-微管连接是桥接或侧向的。然而,在后期 II 开始时,只有不到 1%的染色体在纺锤体赤道处滞后,不到 10%的滞后染色体错误分离并产生非整倍体配子。我们的结果表明,在第二次减数分裂的中期阶段,异常的动粒-微管连接没有得到纠正。因此,在减数分裂 II 过程中,小鼠卵母细胞中染色体分离过程的准确性是通过在后期阶段进行的有效校正过程来保证的。