Kotani Tomoya, Yamashita Masakane
Laboratory of Molecular and Cellular Interactions, Division of Biological Sciences, Graduate School of Science, Hokkaido University, Sapporo 060-0810, Japan.
Biochem J. 2005 Aug 1;389(Pt 3):611-7. doi: 10.1042/BJ20050243.
Mechanisms of spindle pole formation rely on minus-end-directed motor proteins. gamma-Tubulin is present at the centre of poles, but its function during pole formation is completely unknown. To address the role of gamma-tubulin in spindle pole formation, we overexpressed GFP (green fluorescent protein)-fused gamma-tubulin (gamma-Tu-GFP) in Xenopus oocytes and produced self-assembled mitotic asters in the oocyte extracts. gamma-Tu-GFP associated with endogenous alpha-, beta- and gamma-tubulin, suggesting that it acts in the same manner as that of endogenous gamma-tubulin. During the process of aster formation, gamma-Tu-GFP aggregated as dots on microtubules, and then the dots were translocated to the centre of the aster along microtubules in a manner dependent on cytoplasmic dynein activity. Inhibition of the function of gamma-tubulin by an anti-gamma-tubulin antibody resulted in failure of microtubule organization into asters. This defect was restored by overexpression of gamma-Tu-GFP, confirming the necessity of gamma-tubulin in microtubule recruitment for aster formation. We also examined the effects of truncated gamma-tubulin mutants, which are difficult to solubly express in other systems, on aster formation. The middle part of gamma-tubulin caused abnormal organization of microtubules in which minus ends of microtubules were not tethered, but dispersed. An N-terminus-deleted mutant prevented recruitment of microtubules into asters, similar to the effect of the anti-gamma-tubulin antibody. The results indicate possible roles of gamma-tubulin in spindle pole formation and show that the system developed in the present study could be useful for analysing roles of many proteins that are difficult to solubly express.
纺锤体极形成的机制依赖于向负端移动的驱动蛋白。γ-微管蛋白存在于纺锤体极的中心,但其在极形成过程中的功能完全未知。为了探究γ-微管蛋白在纺锤体极形成中的作用,我们在非洲爪蟾卵母细胞中过表达了绿色荧光蛋白(GFP)融合的γ-微管蛋白(γ-Tu-GFP),并在卵母细胞提取物中产生了自组装的有丝分裂星状体。γ-Tu-GFP与内源性α-、β-和γ-微管蛋白相关联,表明它与内源性γ-微管蛋白的作用方式相同。在星状体形成过程中,γ-Tu-GFP聚集在微管上形成点状物,然后这些点状物沿着微管以依赖于胞质动力蛋白活性的方式转移到星状体的中心。用抗γ-微管蛋白抗体抑制γ-微管蛋白的功能导致微管无法组织形成星状体。通过过表达γ-Tu-GFP可恢复此缺陷,证实了γ-微管蛋白在微管募集形成星状体中的必要性。我们还研究了截短的γ-微管蛋白突变体对星状体形成的影响,这些突变体在其他系统中难以可溶性表达。γ-微管蛋白的中间部分导致微管异常组织,其中微管的负端未被束缚,而是分散的。一个缺失N端的突变体阻止微管募集到星状体中,类似于抗γ-微管蛋白抗体的作用。结果表明γ-微管蛋白在纺锤体极形成中可能发挥的作用,并表明本研究中开发的系统可用于分析许多难以可溶性表达的蛋白质的作用。