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盘基网柄菌胞质γ-微管蛋白复合体的分子分析

Molecular analysis of the cytosolic Dictyostelium gamma-tubulin complex.

作者信息

Daunderer Christine, Gräf Ralph O

机构信息

Adolf-Butenandt-Institut/Zellbiologie, Universität München, Germany.

出版信息

Eur J Cell Biol. 2002 Apr;81(4):175-84. doi: 10.1078/0171-9335-00241.

Abstract

gamma-Tubulin plays an essential role in microtubule nucleation and organization and occurs, besides its centrosomal localization, in the cytosol, where it forms soluble complexes with other proteins. We investigated the size and composition of gamma-tubulin complexes in Dictyostelium, using a mutant cell line in which the endogenous copy of the gamma-tubulin gene had been replaced by a tagged version. Dictyostelium gamma-tubulin complexes were generally much smaller than the large gamma-tubulin ring complexes found in higher organisms. The stability of the small Dictyostelium gamma-tubulin complexes depended strongly on the purification conditions, with a striking stabilization of the complexes under high salt conditions. Furthermore, we cloned the Dictyostelium homolog of Spc97 and an almost complete sequence of the Dictyostelium homolog of Spc98, which are both components of gamma-tubulin complexes in other organisms. Both proteins localize to the centrosome in Dictyostelium throughout the cell cycle and are also present in a cytosolic pool. We could show that the prevailing small complex present in Dictyostelium consists of DdSpc98 and gamma-tubulin, whereas DdSpc97 does not associate. Dictyostelium is thus the first organism investigated so far where the three proteins do not interact stably in the cytosol.

摘要

γ-微管蛋白在微管成核和组织过程中发挥着重要作用,除了定位于中心体之外,还存在于细胞质中,在细胞质中它与其他蛋白质形成可溶性复合物。我们使用一种突变细胞系研究了盘基网柄菌中γ-微管蛋白复合物的大小和组成,在该突变细胞系中,γ-微管蛋白基因的内源性拷贝已被一个带标签的版本所取代。盘基网柄菌的γ-微管蛋白复合物通常比在高等生物中发现的大型γ-微管蛋白环复合物小得多。小型盘基网柄菌γ-微管蛋白复合物的稳定性在很大程度上取决于纯化条件,在高盐条件下复合物会有显著的稳定。此外,我们克隆了Spc97的盘基网柄菌同源物以及Spc98的盘基网柄菌同源物的几乎完整序列,这两种蛋白在其他生物中都是γ-微管蛋白复合物的组成成分。这两种蛋白在盘基网柄菌整个细胞周期中都定位于中心体,并且也存在于细胞质池中。我们能够证明,盘基网柄菌中普遍存在的小型复合物由DdSpc98和γ-微管蛋白组成,而DdSpc97不与之结合。因此,盘基网柄菌是迄今为止所研究的第一种在细胞质中这三种蛋白不稳定相互作用的生物。

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