
Centrosomes provide a "timely two-ness" to mitotic spindle organization that allows cell division to occur without a spindle assembly checkpoint (SAC)-dependent mitotic delay.


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The spindle assembly checkpoint (SAC) temporally regulates mitosis by preventing progression from metaphase to anaphase until all chromosomes are correctly attached to the mitotic spindle. Centrosomes refine the spatial organization of the mitotic spindle at the spindle poles. However, centrosome loss leads to elongated mitosis, suggesting that centrosomes also inform the temporal organization of mitosis in mammalian cells. Here we find that the mitotic delay in acentrosomal cells is enforced by the SAC in a MPS1-dependent manner, and that a SAC-dependent mitotic delay is required for bipolar cell division to occur in acentrosomal cells. Although acentrosomal cells become polyploid, polyploidy is not sufficient to cause dependency on a SAC-mediated delay to complete cell division. Rather, the division failure in absence of MPS1 activity results from mitotic exit occurring before acentrosomal spindles can become bipolar. Furthermore, prevention of centrosome separation suffices to make cell division reliant on a SAC-dependent mitotic delay. Thus, centrosomes and their definition of two spindle poles early in mitosis provide a “timely two-ness” that allows cell division to occur in absence of a SAC-dependent mitotic delay.

### Competing Interest Statement

The authors have declared no competing interest.

Spindle assembly checkpoint-dependent mitotic delay is required for cell division in absence of centrosomes

centrosome-loss-requires-spindle-assembly-checkpoint-dependent-mitotic-delay-for-successful-cell-division


Centrosome Loss Requires Spindle Assembly Checkpoint-Dependent Mitotic Delay for Successful Cell Division
