Humphrey Oei Institute of Cancer Research, National Cancer Centre, Singapore, Singapore.
Cell Death Differ. 2010 May;17(5):787-800. doi: 10.1038/cdd.2009.181. Epub 2009 Dec 11.
The molecular mechanisms regulating cell death during mitosis are poorly understood. We show here a critical role for p73, but not p53, in regulating mitotic cell death induced by various means. Prolonged mitotic arrest and the activation of spindle checkpoint are required for mitotic death, which occurs before mitotic exit and which can be ameliorated by accelerated mitotic exit. Absence or silencing of p73 expression abrogated mitotic death without accelerating mitotic exit, and was independent of BubR1 and Mad2, the loss of which promotes mitotic exit. However, the absence of p73 reduced mitotic death by compromising the expression of the proapoptotic BH3-only protein Bim and thereby affecting cytochrome c release and caspase activation. p73 was found to induce bim expression through direct binding to regulatory elements in intron 1. Congruently, mitotic cell death was rescued to similar extents by silencing either bim or p73 expression. Taken together, the data show an important role for the p73-Bim axis in regulating cell death during mitosis that is independent of p53.
目前对于调控有丝分裂细胞死亡的分子机制还知之甚少。我们在此展示了 p73 (而非 p53 )在调控多种手段诱导的有丝分裂细胞死亡中起着关键作用。有丝分裂阻滞延长和纺锤体检查点的激活是诱导有丝分裂死亡的必要条件,有丝分裂死亡发生在有丝分裂退出之前,可以通过加速有丝分裂退出来减轻。p73 表达的缺失或沉默消除了有丝分裂死亡而没有加速有丝分裂退出,并且与 BubR1 和 Mad2 无关,BubR1 和 Mad2 的缺失会促进有丝分裂退出。然而,p73 的缺失通过降低促凋亡 BH3 仅蛋白 Bim 的表达而损害有丝分裂死亡,从而影响细胞色素 c 的释放和半胱天冬酶的激活。发现 p73 通过直接结合内含子 1 中的调节元件来诱导 bim 表达。一致地,沉默 bim 或 p73 的表达在相似程度上挽救了有丝分裂细胞死亡。总之,数据表明 p73-Bim 轴在调控有丝分裂细胞死亡中起着重要作用,这与 p53 无关。