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Novel Response to Microtubule Perturbation in Meiosis

机译:对减数分裂中微管摄动的新反应。

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During the mitotic cell cycle, microtubule depolymerization leads to a cell cycle arrest in metaphase, due to activation of the spindle checkpoint. Here, we show that under microtubule-destabilizing conditions, such as low temperature or the presence of the spindle-depolymerizing drug benomyl, meiotic budding yeast cells arrest in G1 or G2, instead of metaphase. Cells arrest in G1 if microtubule perturbation occurs as they enter the meiotic cell cycle and in G2 if cells are already undergoing premeiotic S phase. Concomitantly, cells down-regulate genes required for cell cycle progression, meiotic differentiation, and spore formation in a highly coordinated manner. Decreased expression of these genes is likely to be responsible for halting both cell cycle progression and meiotic development. Our results point towards the existence of a novel surveillance mechanism of microtubule integrity that may be particularly important during specialized cell cycles when coordination of cell cycle progression with a developmental program is necessary.
机译:在有丝分裂细胞周期中,由于纺锤体检查点的激活,微管解聚导致细胞周期停滞在中期。在这里,我们显示了在微管破坏条件下,例如低温或纺锤体解聚药物苯菌灵的存在,减数分裂芽胞酵母细胞停滞在G 1 或G 2 ,而不是中期。如果细胞进入减数分裂细胞周期时发生微管扰动,则细胞会停滞在G 1 中;如果细胞已经处于减数分裂前S期,则会停滞在G 2 中。同时,细胞以高度协调的方式下调了细胞周期进程,减数分裂分化和孢子形成所需的基因。这些基因的表达下降可能是导致细胞周期进程和减数分裂发育停止的原因。我们的研究结果表明,存在一种新型的微管完整性监测机制,在专门的细胞周期中,当需要协调细胞周期进程与发育程序时,这一机制可能特别重要。

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