Cross S M, Sanchez C A, Morgan C A, Schimke M K, Ramel S, Idzerda R L, Raskind W H, Reid B J
Department of Medicine, University of Washington, Seattle 98195.
Science. 1995 Mar 3;267(5202):1353-6. doi: 10.1126/science.7871434.
Cell cycle checkpoints enhance genetic fidelity by causing arrest at specific stages of the cell cycle when previous events have not been completed. The tumor suppressor p53 has been implicated in a G1 checkpoint. To investigate whether p53 also participates in a mitotic checkpoint, cultured fibroblasts from p53-deficient mouse embryos were exposed to spindle inhibitors. The fibroblasts underwent multiple rounds of DNA synthesis without completing chromosome segregation, thus forming tetraploid and octaploid cells. Deficiency of p53 was also associated with the development of tetraploidy in vivo. These results suggest that murine p53 is a component of a spindle checkpoint that ensures the maintenance of diploidy.
细胞周期检查点通过在细胞周期的特定阶段导致停滞来增强遗传保真度,前提是先前的事件尚未完成。肿瘤抑制因子p53与G1期检查点有关。为了研究p53是否也参与有丝分裂检查点,将来自p53缺陷型小鼠胚胎的培养成纤维细胞暴露于纺锤体抑制剂。这些成纤维细胞经历了多轮DNA合成,但未完成染色体分离,从而形成了四倍体和八倍体细胞。p53的缺陷也与体内四倍体的形成有关。这些结果表明,小鼠p53是纺锤体检查点的一个组成部分,可确保维持二倍体状态。