Division of Life Science, Center for Cancer Research, and State Key Laboratory of Molecular Neuroscience, Hong Kong University of Science and Technology, Clear Water Bay, Hong Kong.
Department of Molecular Biosciences, Institute for Cellular and Molecular Biology, The University of Texas at Austin, Austin, TX, USA.
Oncogene. 2020 Mar;39(13):2819-2834. doi: 10.1038/s41388-020-1187-6. Epub 2020 Feb 6.
Mitotic slippage involves cells exiting mitosis without proper chromosome segregation. Although degradation of cyclin B1 during prolonged mitotic arrest is believed to trigger mitotic slippage, its upstream regulation remains obscure. Whether mitotic slippage is caused by APC/C activity that is able to escape spindle-assembly checkpoint (SAC)-mediated inhibition, or is actively promoted by a change in SAC activity remains an outstanding issue. We found that a major culprit for mitotic slippage involves reduction of MAD2 at the kinetochores, resulting in a progressive weakening of SAC during mitotic arrest. A further level of control of the timing of mitotic slippage is through p31-mediated suppression of MAD2 activation. The loss of kinetochore MAD2 was dependent on APC/C, indicating a feedback control of APC/C to SAC during prolonged mitotic arrest. The gradual weakening of SAC during mitotic arrest enables APC/C to degrade cyclin B1, cumulating in the cell exiting mitosis by mitotic slippage.
有丝分裂滑动用细胞在没有正确染色体分离的情况下退出有丝分裂。虽然在长时间有丝分裂阻滞期间,细胞周期蛋白 B1 的降解被认为会触发有丝分裂滑动用细胞在没有正确染色体分离的情况下退出有丝分裂。虽然在长时间有丝分裂阻滞期间,细胞周期蛋白 B1 的降解被认为会触发有丝分裂滑动用细胞在没有正确染色体分离的情况下退出有丝分裂。虽然在长时间有丝分裂阻滞期间,细胞周期蛋白 B1 的降解被认为会触发有丝分裂滑动用细胞在没有正确染色体分离的情况下退出有丝分裂。但是,有丝分裂滑动用细胞是否是由能够逃避纺锤体组装检查点(SAC)介导的抑制的 APC/C 活性引起的,或者是否是由 SAC 活性的改变主动促进的,仍然是一个悬而未决的问题。我们发现,有丝分裂滑动用细胞的一个主要罪魁祸首涉及动粒处 MAD2 的减少,导致有丝分裂阻滞期间 SAC 逐渐减弱。通过 p31 介导的 MAD2 激活抑制进一步控制有丝分裂滑动用细胞的时机。动粒 MAD2 的缺失依赖于 APC/C,表明 APC/C 在长时间有丝分裂阻滞期间对 SAC 的反馈控制。有丝分裂阻滞期间 SAC 的逐渐减弱使 APC/C 能够降解细胞周期蛋白 B1,从而导致细胞通过有丝分裂滑动用细胞退出有丝分裂。