Inserm Unit 366, DRDC/CS, CEA-Grenoble, Grenoble, France.
PLoS One. 2010 Feb 17;5(2):e9248. doi: 10.1371/journal.pone.0009248.
In metazoan oocytes the assembly of a microtubule-based spindle depends on the activity of a large number of accessory non-tubulin proteins, many of which remain unknown. In this work we isolated the microtubule-bound proteins from Xenopus eggs. Using mass spectrometry we identified 318 proteins, only 43 of which are known to bind microtubules. To integrate our results, we compiled for the first time a network of the meiotic microtubule-related interactome. The map reveals numerous interactions between spindle microtubules and the newly identified non-tubulin spindle components and highlights proteins absent from the mitotic spindle proteome. To validate newly identified spindle components, we expressed as GFP-fusions nine proteins identified by us and for first time demonstrated that Mgc68500, Loc398535, Nif3l1bp1/THOC7, LSM14A/RAP55A, TSGA14/CEP41, Mgc80361 and Mgc81475 are associated with spindles in egg extracts or in somatic cells. Furthermore, we showed that transfection of HeLa cells with siRNAs, corresponding to the human orthologue of Mgc81475 dramatically perturbs spindle formation in HeLa cells. These results show that our approach to the identification of the Xenopus microtubule-associated proteome yielded bona fide factors with a role in spindle assembly.
在后生动物卵母细胞中,微管为基础的纺锤体的组装依赖于大量辅助非微管蛋白的活性,其中许多仍然未知。在这项工作中,我们从非洲爪蟾卵中分离了微管结合蛋白。通过质谱分析,我们鉴定了 318 种蛋白质,其中只有 43 种已知与微管结合。为了整合我们的结果,我们首次编制了一个减数分裂微管相关相互作用组的网络图。该图谱揭示了纺锤体微管与新鉴定的非微管纺锤体成分之间的许多相互作用,并突出了不存在于有丝分裂纺锤体蛋白质组中的蛋白质。为了验证新鉴定的纺锤体成分,我们以 GFP 融合的形式表达了我们鉴定的 9 种蛋白质,并首次证明 Mgc68500、Loc398535、Nif3l1bp1/THOC7、LSM14A/RAP55A、TSGA14/CEP41、Mgc80361 和 Mgc81475 与卵提取物或体细胞中的纺锤体有关。此外,我们还表明,用针对 Mgc81475 人同源物的 siRNA 转染 HeLa 细胞,会严重干扰 HeLa 细胞中纺锤体的形成。这些结果表明,我们鉴定非洲爪蟾微管相关蛋白质组的方法产生了真正参与纺锤体组装的因子。