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Arabidopsis Cell Division Cycle 20.1 Is Required for Normal Meiotic Spindle Assembly and Chromosome Segregation

机译:正常减数分裂主轴组装和染色体分离需要拟南芥细胞分裂周期20.1。

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Cell division requires proper spindle assembly; a surveillance pathway, the spindle assembly checkpoint (SAC), monitors whether the spindle is normal and correctly attached to kinetochores. The SAC proteins regulate mitotic chromosome segregation by affecting CDC20 (Cell Division Cycle 20) function. However, it is unclear whether CDC20 regulates meiotic spindle assembly and proper homolog segregation. Here, we show that the Arabidopsis thaliana CDC20.1 gene is indispensable for meiosis and male fertility. We demonstrate that cdc20.1 meiotic chromosomes align asynchronously and segregate unequally and the metaphase I spindle has aberrant morphology. Comparison of the distribution of meiotic stages at different time points between the wild type and cdc20.1 reveals a delay of meiotic progression from diakinesis to anaphase I. Furthermore, cdc20.1 meiocytes exhibit an abnormal distribution of a histone H3 phosphorylation mark mediated by the Aurora kinase, providing evidence that CDC20.1 regulates Aurora localization for meiotic chromosome segregation. Further evidence that CDC20.1 and Aurora are functionally related was provided by meiosis-specific knockdown of At-Aurora1 expression, resulting in meiotic chromosome segregation defects similar to those of cdc20.1. Taken together, these results suggest a critical role for CDC20.1 in SAC-dependent meiotic chromosome segregation.
机译:细胞分裂需要正确的主轴组装;监视路径,即主轴组件检查点(SAC),监视主轴是否正常以及是否正确连接到动植物。 SAC蛋白通过影响CDC20(细胞分裂周期20)功能来调节有丝分裂染色体的分离。但是,尚不清楚CDC20是否调节减数分裂纺锤体组装和适当的同源分离。在这里,我们显示拟南芥CDC20.1基因对于减数分裂和雄性育性是必不可少的。我们证明,cdc20.1减数分裂染色体异步排列和不平等地分离,中期I纺锤体具有异常的形态。比较野生型和cdc20.1在不同时间点的减数分裂阶段的分布,揭示了减数分裂从迟发性疾病到后期I的延迟。此外,cdc20.1减数分裂细胞表现出由HCC介导的组蛋白H3磷酸化标记的异常分布。 Aurora激酶,提供CDC20.1调节减数分裂染色体分离的Aurora定位的证据。通过减数分裂特定的At-Aurora1表达的减数分裂,提供了CDC20.1和Aurora在功能上相关的进一步证据,导致减数分裂染色体分离缺陷与cdc20.1相似。综上所述,这些结果表明CDC20.1在SAC依赖的减数分裂染色体分离中起着至关重要的作用。

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