首页> 美国卫生研究院文献>The EMBO Journal >The spindle pole body component Spc97p interacts with the gamma-tubulin of Saccharomyces cerevisiae and functions in microtubule organization and spindle pole body duplication.
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The spindle pole body component Spc97p interacts with the gamma-tubulin of Saccharomyces cerevisiae and functions in microtubule organization and spindle pole body duplication.

机译:纺锤极体成分Spc97p与酿酒酵母的γ-微管蛋白相互作用并在微管组织和纺锤极体复制中起作用。

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摘要

Previously, we have shown that the gamma-tubulin Tub4p and the spindle pole body component Spc98p are involved in microtubule organization by the yeast microtubule organizing centre, the spindle pole body (SPB). In this paper we report the identification of SPC97 encoding an essential SPB component that is in association with the SPB substructures that organize the cytoplasmic and nuclear microtubules. Evidence is provided for a physical and functional interaction between Tub4p, Spc98p and Spc97p: first, temperature-sensitive spc97(ts) mutants are suppressed by high gene dosage of SPC98 or TUB4. Second, Spc97p interacts with Spc98p and Tub4p in the two-hybrid system. Finally, immunoprecipitation and fractionation studies revealed complexes containing Tub4p, Spc98p and Spc97p. Further support for a direct interaction of Tub4p, Spc98p and Spc97p comes from the toxicity of strong SPC97 overexpression which is suppressed by co-overexpression of TUB4 or SPC98. Analysis of temperature-sensitive spc97(ts) alleles revealed multiple spindle defects. While spc97-14 cells are either impaired in SPB separation or mitotic spindle formation, spc97-20 cells show an additional defect in SPB duplication. We discuss a model in which the Tub4p-Spc98p-Spc97p complex is part of the microtubule attachment site at the SPB.
机译:以前,我们已经表明,酵母微管组织中心,纺锤极体(SPB)参与了γ-微管蛋白Tub4p和纺锤极体组件Spc98p的微管组织。在本文中,我们报告鉴定了编码必需的SPB组件的SPC97,该SPB组件与组织细胞质和核微管的SPB子结构相关。提供了Tub4p,Spc98p和Spc97p之间的物理和功能相互作用的证据:首先,通过高基因剂量的SPC98或TUB4抑制温度敏感的spc97(ts)突变体。其次,Spc97p在双杂交系统中与Spc98p和Tub4p相互作用。最后,免疫沉淀和分级分离研究揭示了含有Tub4p,Spc98p和Spc97p的复合物。 Tub4p,Spc98p和Spc97p直接相互作用的进一步支持来自强大的SPC97过表达的毒性,这种毒性被TUB4或SPC98的共过表达所抑制。对温度敏感的spc97(ts)等位基因的分析揭示了多个纺锤体缺陷。尽管spc97-14细胞在SPB分离或有丝分裂纺锤体形成中受损,但spc97-20细胞在SPB复制中显示了另一个缺陷。我们讨论了其中Tub4p-Spc98p-Spc97p复合体是SPB上微管附着位点的一部分的模型。

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