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通过对粟酒裂殖酵母中gtb1和alp4突变的抑制分析对γ-微管蛋白复合体进行功能剖析。

Functional dissection of the gamma-tubulin complex by suppressor analysis of gtb1 and alp4 mutations in Schizosaccharomyces pombe.

作者信息

Tange Yoshie, Fujita Akiko, Toda Takashi, Niwa Osami

机构信息

Kazusa DNA Research Institute, Kisarazu, Chiba 292-0818, Japan.

出版信息

Genetics. 2004 Jul;167(3):1095-107. doi: 10.1534/genetics.104.027946.

Abstract

In fission yeast, gamma-tubulin (encoded by the gtb1+ gene), Alp4 (Spc97/GCP2), and Alp6 (Spc98/GCP3) are essential components of the gamma-tubulin complex. We isolated gtb1 mutants as allele-specific suppressors of temperature-sensitive alp4 mutations. Mutation sites in gtb1 mutants and in several alp4 alleles were determined. The majority of substituted amino acids were mapped to a small area on the predicted surface of the gamma-tubulin molecule that might directly interact with the Alp4 protein. The cold sensitivity of gamma-tubulin mutants was almost completely suppressed by an alpha-tubulin mutation and partially suppressed by a low concentration of thiabendazole, a microtubule assembly inhibitor. Other gtb1 mutants had increased resistance to this drug. Gel-filtration and immunoprecipitation analyses suggested that the mutant gamma-tubulin formed an altered gamma-tubulin complex with increased stability compared to wild-type gamma-tubulin. In most gtb1 mutants, sexual development was impaired, and aberrant asci that contained an irregular spore shape and number were produced. In contrast, spore formation was not appreciably damaged in some alp4 and alp6 mutants, even at temperatures where vegetative proliferation was substantially defective. These results suggested that the function of the gamma-tubulin complex or the requirement of each component of the complex is differentially regulated between the vegetative and sexual phases of the life cycle in fission yeast. In addition, genetic data indicated intimate functional connections of gamma-tubulin with several kinesin-like proteins.

摘要

在裂殖酵母中,γ-微管蛋白(由gtb1⁺基因编码)、Alp4(Spc97/GCP2)和Alp6(Spc98/GCP3)是γ-微管蛋白复合体的重要组成部分。我们分离出gtb1突变体作为温度敏感型alp4突变的等位基因特异性抑制子。确定了gtb1突变体和几个alp4等位基因中的突变位点。大多数被取代的氨基酸被定位到γ-微管蛋白分子预测表面的一个小区域,该区域可能直接与Alp4蛋白相互作用。γ-微管蛋白突变体的冷敏感性几乎完全被α-微管蛋白突变所抑制,并且被低浓度的噻苯咪唑(一种微管组装抑制剂)部分抑制。其他gtb1突变体对这种药物的抗性增加。凝胶过滤和免疫沉淀分析表明,与野生型γ-微管蛋白相比,突变型γ-微管蛋白形成了一种稳定性增加的改变的γ-微管蛋白复合体。在大多数gtb1突变体中,有性发育受损,并产生了含有不规则孢子形状和数量的异常子囊。相比之下,在一些alp4和alp6突变体中,即使在营养增殖严重缺陷的温度下,孢子形成也没有明显受损。这些结果表明,γ-微管蛋白复合体的功能或复合体各组分的需求在裂殖酵母生命周期的营养期和有性期之间受到不同的调控。此外,遗传数据表明γ-微管蛋白与几种驱动蛋白样蛋白存在密切的功能联系。

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本文引用的文献

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