Sundberg H A, Davis T N
Department of Biochemistry, University of Washington, Seattle, Washington 98195-7350, USA.
Mol Biol Cell. 1997 Dec;8(12):2575-90. doi: 10.1091/mbc.8.12.2575.
The central coiled coil of the essential spindle pole component Spc110p spans the distance between the central and inner plaques of the Saccharomyces cerevisiae spindle pole body (SPB). The carboxy terminus of Spc110p, which binds calmodulin, resides at the central plaque, and the amino terminus resides at the inner plaque from which nuclear microtubules originate. To dissect the functions of Spc110p, we created temperature-sensitive mutations in the amino and carboxy termini. Analysis of the temperature-sensitive spc110 mutations and intragenic complementation analysis of the spc110 alleles defined three functional regions of Spc110p. Region I is located at the amino terminus. Region II is located at the carboxy-terminal end of the coiled coil, and region III is the previously defined calmodulin-binding site. Overexpression of SPC98 suppresses the temperature sensitivity conferred by mutations in region I but not the phenotypes conferred by mutations in the other two regions, suggesting that the amino terminus of Spc110p is involved in an interaction with the gamma-tubulin complex composed of Spc97p, Spc98p, and Tub4p. Mutations in region II lead to loss of SPB integrity during mitosis, suggesting that this region is required for the stable attachment of Spc110p to the central plaque. Our results strongly argue that Spc110p links the gamma-tubulin complex to the central plaque of the SPB.
重要的纺锤体极组件Spc110p的中央卷曲螺旋跨越酿酒酵母纺锤体极体(SPB)中央斑和内斑之间的距离。Spc110p的羧基末端与钙调蛋白结合,位于中央斑,而氨基末端位于核微管起源的内斑。为了剖析Spc110p的功能,我们在氨基末端和羧基末端创建了温度敏感突变。对温度敏感的spc110突变的分析以及spc110等位基因的基因内互补分析确定了Spc110p的三个功能区域。区域I位于氨基末端。区域II位于卷曲螺旋的羧基末端,区域III是先前定义的钙调蛋白结合位点。SPC98的过表达抑制了区域I突变赋予的温度敏感性,但不抑制其他两个区域突变赋予的表型,这表明Spc110p的氨基末端参与了与由Spc97p、Spc98p和Tub4p组成的γ-微管蛋白复合体的相互作用。区域II的突变导致有丝分裂期间SPB完整性丧失,表明该区域是Spc110p稳定附着于中央斑所必需的。我们的结果有力地表明,Spc110p将γ-微管蛋白复合体与SPB的中央斑连接起来。