Boleti H, Karsenti E, Vernos I
Cell Biology Programme, European Molecular Biology Laboratory, Heidelberg, Federal Republic of Germany.
Cell. 1996 Jan 12;84(1):49-59. doi: 10.1016/s0092-8674(00)80992-7.
We describe a novel Xenopus plus end-directed kinesin-like protein (KLP), Xklp2, localized on centrosomes throughout the cell cycle and on spindle pole microtubules during metaphase. Using mitotic spindles assembled in Xenopus egg extracts and different recombinant GST-Xklp2 mutants, we show that this motor is targeted to spindle poles through its C-terminal domain. Xklp2-truncated polypeptides lacking the motor domain block centrosome separation and disrupt preassembled metaphase spindles. Antibodies directed against the tail of Xklp2 have a similar effect. These results show that Xklp2 protein is required for centrosome separation and maintenance of spindle bipolarity. This study is an example of the application of the dominant negative mutant effect on spindle assembly in Xenopus egg extracts, demonstrating the usefulness of this approach in probing the function of proteins in this system.
我们描述了一种新的非洲爪蟾加端定向驱动蛋白样蛋白(KLP),即Xklp2,它在整个细胞周期中定位于中心体,在中期定位于纺锤体极微管。利用在非洲爪蟾卵提取物中组装的有丝分裂纺锤体和不同的重组GST-Xklp2突变体,我们表明这种马达蛋白通过其C末端结构域靶向纺锤体极。缺少马达结构域的Xklp2截短多肽会阻止中心体分离并破坏预先组装好的中期纺锤体。针对Xklp2尾部的抗体有类似作用。这些结果表明Xklp2蛋白是中心体分离和纺锤体双极性维持所必需的。这项研究是显性负突变效应在非洲爪蟾卵提取物纺锤体组装中的应用实例,证明了这种方法在探究该系统中蛋白质功能方面的有用性。