Balestra Fernando R, Jimenez Juan
Centro Andaluz de Biologia del Desarrollo, Universidad Pablo de Olavide/CSIC, Carretera de Utrera, Km1, 41013 Sevilla, Spain.
Genetics. 2008 Dec;180(4):2073-80. doi: 10.1534/genetics.108.094797. Epub 2008 Oct 9.
Microtubules assume a variety of structures throughout the different stages of the cell cycle. Ensuring the correct assembly of such structures is essential to guarantee cell division. During mitosis, it is well established that the spindle assembly checkpoint monitors the correct attachment of sister chromatids to the mitotic spindle. However, the role that microtubule cytoskeleton integrity plays for cell-cycle progression during interphase is uncertain. Here we describe the existence of a mechanism, independent of the mitotic checkpoint, that delays entry into mitosis in response to G(2)-phase microtubule damage. Disassembly of the G(2)-phase microtubule array leads to the stabilization of the universal mitotic inhibitor Wee1, thus actively delaying entry into mitosis via inhibitory Cdc2 Tyr15 phosphorylation.
微管在细胞周期的不同阶段呈现出多种结构。确保这些结构的正确组装对于保证细胞分裂至关重要。在有丝分裂期间,纺锤体组装检查点监测姐妹染色单体与有丝分裂纺锤体的正确附着,这一点已得到充分证实。然而,微管细胞骨架完整性在间期细胞周期进程中所起的作用尚不确定。在此,我们描述了一种独立于有丝分裂检查点的机制的存在,该机制响应G2期微管损伤而延迟进入有丝分裂。G2期微管阵列的解聚导致通用有丝分裂抑制剂Wee1的稳定,从而通过抑制性Cdc2 Tyr15磷酸化积极延迟进入有丝分裂。