Cao Kan, Nakajima Reiko, Meyer Hemmo H, Zheng Yixian
Department of Embryology, Carnegie Institution of Washington and Howard Hughes Medical Institute, Baltimore, MD 21210, USA.
Cell. 2003 Oct 31;115(3):355-67. doi: 10.1016/s0092-8674(03)00815-8.
Spindle disassembly at the end of mitosis is a complex and poorly understood process. Here, we report that the AAA-ATPase Cdc48/p97 and its adapters Ufd1-Npl4, which have a well-established role in membrane functions, also regulate spindle disassembly by modulating microtubule dynamics and bundling at the end of mitosis. In the absence of p97-Ufd1-Npl4 function, microtubules in Xenopus egg extracts remain as monopolar spindles attached to condensed chromosomes after Cdc2 kinase activity has returned to the interphase level. Consequently, interphase microtubule arrays and nuclei are not established. Genetic analyses of Cdc48, the yeast homolog of p97, reveal that Cdc48 is also required for disassembly of mitotic spindles after execution of the mitotic exit pathway. Furthermore, Cdc48/p97-Ufd1-Npl4 directly binds to spindle assembly factors and regulates their interaction with microtubules at the end of mitosis. Therefore, Cdc48/p97-Ufd1-Npl4 is an essential chaperone that regulates transformation of the microtubule structure as cells reenter interphase.
有丝分裂末期纺锤体的解体是一个复杂且尚未被充分理解的过程。在此,我们报告AAA-ATP酶Cdc48/p97及其衔接蛋白Ufd1-Npl4,它们在膜功能方面有着既定作用,在有丝分裂末期还通过调节微管动力学和微管束集来调控纺锤体解体。在缺乏p97-Ufd1-Npl4功能的情况下,非洲爪蟾卵提取物中的微管在Cdc2激酶活性恢复到间期水平后,仍作为附着于浓缩染色体的单极纺锤体存在。因此,间期微管阵列和细胞核无法形成。对p97的酵母同源物Cdc48进行的遗传学分析表明,在有丝分裂退出途径执行后,Cdc48对于有丝分裂纺锤体的解体也是必需的。此外,Cdc48/p97-Ufd1-Npl4直接结合纺锤体组装因子,并在有丝分裂末期调节它们与微管的相互作用。因此,Cdc48/p97-Ufd1-Npl4是一种重要的伴侣蛋白,在细胞重新进入间期时调节微管结构的转变。