Mitotic slippage is determined by p31 and the weakening of the spindle-assembly checkpoint.

Oncogene

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.

Published: March 2020

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.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7098889PMC
http://dx.doi.org/10.1038/s41388-020-1187-6DOI Listing

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