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酵母纺锤体极体组件之间的直接相互作用:Kar1p是Cdc31p定位于纺锤体极体所必需的。

Direct interaction between yeast spindle pole body components: Kar1p is required for Cdc31p localization to the spindle pole body.

作者信息

Biggins S, Rose M D

机构信息

Department of Molecular Biology, Princeton University, New Jersey 08544-1014.

出版信息

J Cell Biol. 1994 May;125(4):843-52. doi: 10.1083/jcb.125.4.843.

Abstract

The Saccharomyces cerevisiae genes KAR1 and CDC31 are required for the initial stages of spindle pole body (SPB) duplication in yeast. The Cdc31 protein is most related to caltractin/centrin, a calcium-binding protein present in microtubule organizing centers in many organisms. Because of a variety of genetic interactions between CDC31 and KAR1 (Vallen, E. A., W. Ho. M. Winey, and M. D. Rose. 1994. Genetics. In press), we wanted to determine whether Cdc31p and Kar1p physically interact. Cdc31p was expressed and purified from Escherichia coli and active for binding calcium. Using a protein blotting technique, Cdc31p bound to Kar1p in vitro via an essential domain in Kar1p required for SPB duplication (Vallen, E. A., M. A. Hiller, T. Y. Scherson, and M. D. Rose. 1992a. J. Cell Biol. 117:1277-1287). By immunofluorescence microscopy, we determined that the interaction also occurs in vivo. Cdc31p was localized to the SPB in wild-type cells but was mislocalized in a kar1 mutant strain. In a kar1 mutant containing a dominant CDC31 suppressor, Cdc31p was again localized to the SPB. Furthermore, the localization of Cdc31p to the SPB was affected by the overexpression of Kar1p-beta-galactosidase hybrids. Based on these data, we propose that the essential function of Kar1p is to localize Cdc31p to the SPB, and that this interaction is normally required for SPB duplication.

摘要

酿酒酵母基因KAR1和CDC31是酵母纺锤体极体(SPB)复制初始阶段所必需的。Cdc31蛋白与钙牵蛋白/中心蛋白最为相关,钙牵蛋白/中心蛋白是一种存在于许多生物体微管组织中心的钙结合蛋白。由于CDC31和KAR1之间存在多种遗传相互作用(Vallen, E. A., W. Ho. M. Winey, and M. D. Rose. 1994. Genetics. In press),我们想确定Cdc31p和Kar1p是否存在物理相互作用。Cdc31p在大肠杆菌中表达并纯化,具有结合钙的活性。使用蛋白质印迹技术,Cdc31p在体外通过Kar1p中SPB复制所需的一个必需结构域与Kar1p结合(Vallen, E. A., M. A. Hiller, T. Y. Scherson, and M. D. Rose. 1992a. J. Cell Biol. 117:1277 - 1287)。通过免疫荧光显微镜观察,我们确定这种相互作用在体内也会发生。在野生型细胞中,Cdc31p定位于SPB,但在kar1突变菌株中定位错误。在含有显性CDC31抑制子的kar1突变体中,Cdc31p再次定位于SPB。此外,Kar1p-β-半乳糖苷酶杂种的过表达会影响Cdc31p在SPB的定位。基于这些数据,我们提出Kar1p的基本功能是将Cdc31p定位于SPB,并且这种相互作用通常是SPB复制所必需的。

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本文引用的文献

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