The spindle assembly checkpoint (SAC) delays mitotic progression when chromosomes are not properly attached to microtubules of the mitotic spindle. Cells vary widely in the extent to which they delay mitotic progression upon SAC activation. To explore the mechanisms that determine checkpoint strength in different cells, we systematically measured the mitotic delay induced by microtubule disruption at different stages of embryogenesis in Caenorhabditis elegans. Strikingly, we observed a gradual increase in SAC strength after each round of division. Analysis of mutants that alter cell size or ploidy revealed that SAC strength is determined primarily by cell size and the number of kinetochores. These findings provide clear evidence in vivo that the kinetochore-to-cytoplasm ratio determines the strength of the SAC, providing new insights into why cells exhibit such large variations in their SAC responses.
Cell Size Determines the Strength of the Spindle Assembly Checkpoint during Embryonic Development.
细胞大小决定胚胎发育过程中纺锤体组装检查点的强度
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作者:Galli Matilde, Morgan David O
| 期刊: | Developmental Cell | 影响因子: | 8.700 |
| 时间: | 2016 | 起止号: | 2016 Feb 8; 36(3):344-52 |
| doi: | 10.1016/j.devcel.2016.01.003 | 研究方向: | 细胞生物学 |
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