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Spatiotemporal model for silencing of the mitotic spindle assembly checkpoint
被引:15
作者:
Chen, Jing
[1
]
Liu, Jian
[1
]
机构:
[1] NHLBI, NIH, Bethesda, MD 20892 USA
关键词:
KINETOCHORE-MICROTUBULE INTERFACE;
AURORA-B KINASE;
UNATTACHED KINETOCHORES;
HUMAN-CELLS;
CYCLIN-B;
MAD2;
ACTIVATION;
LIVING CELLS;
DYNAMICS;
MITOSIS;
ANAPHASE;
D O I:
10.1038/ncomms5795
中图分类号:
O [数理科学和化学];
P [天文学、地球科学];
Q [生物科学];
N [自然科学总论];
学科分类号:
07 ;
0710 ;
09 ;
摘要:
The spindle assembly checkpoint arrests mitotic progression until each kinetochore secures a stable attachment to the spindle. Despite fluctuating noise, this checkpoint remains robust and remarkably sensitive to even a single unattached kinetochore among many attached kinetochores; moreover, the checkpoint is silenced only after the final kinetochore-spindle attachment. Experimental observations have shown that checkpoint components stream from attached kinetochores along microtubules towards spindle poles. Here we incorporate this streaming behaviour into a theoretical model that accounts for the robustness of checkpoint silencing. Poleward streams are integrated at spindle poles, but are diverted by any unattached kinetochore; consequently, accumulation of checkpoint components at spindle poles increases markedly only when every kinetochore is properly attached. This step change robustly triggers checkpoint silencing after, and only after, the final kinetochore-spindle attachment. Our model offers a conceptual framework that highlights the role of spatio-temporal regulation in mitotic spindle checkpoint signalling and fidelity of chromosome segregation.
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页数:13
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