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首页> 外文期刊>Journal of cell biology >The Cdc31p-binding protein Kar1p is a component of the half bridge of the yeast spindle pole body.
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The Cdc31p-binding protein Kar1p is a component of the half bridge of the yeast spindle pole body.

机译:Cdc31p结合蛋白Kar1p是酵母纺锤极体半桥的组成部分。

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KAR1 has been identified as an essential gene which is involved in karyogamy of mating yeast cells and in spindle pole body duplication of mitotic cells (Rose, M. D., and G. R. Fink. 1987. Cell. 48:1047-1060). We investigated the cell cycle-dependent localization of the Kar1 protein (Kar1p) and its interaction with other SPB components. Kar1p is associated with the spindle pole body during the entire cell cycle of yeast. Immunoelectron microscopic studies with anti-Kar1p antibodies or with the monoclonal antibody 12CA5 using an epitope-tagged, functional Kar1p revealed that Kar1p is associated with the half bridge or the bridge of the spindle pole body. Cdc31p, a Ca(2+)-binding protein, was previously identified as the first component of the half bridge of the spindle pole body (Spang, A., I. Courtney, U. Fackler, M. Matzner, and E. Schiebel. 1993. J. Cell Biol. 123:405-416). Using an in vitro assay we demonstrate that Cdc31p specifically interacts with a short sequence within the carboxyl terminal half of Kar1p. The potential Cdc31p-binding sequence of Kar1p contains three acidic amino acids which are not found in calmodulin-binding peptides, explaining the different substrate specificities of Cdc31p and calmodulin. Cdc31p was also able to bind to the carboxy terminus of Nuflp/Spc110p, another component of the SPB (Kilmartin, J. V., S. L. Dyos, D. Kershaw, and J. T. Finch. 1993. J. Cell Biol. 123:1175-1184). The association of Kar1p with the spindle pole body was independent of Cdc31p. Cdc31p, on the other hand, was not associated with SPBs of kar1 cells.
机译:KAR1已被鉴定为必需基因,其参与交配酵母细胞的核配体和有丝分裂细胞的纺锤极体复制(Rose,M.D。和G.R.Fink.1987.Cell.48:1047-1060)。我们研究了Kar1蛋白(Kar1p)的细胞周期依赖性定位及其与其他SPB组件的相互作用。在酵母的整个细胞周期中,Kar1p与纺锤极体有关。用抗Kar1p抗体或单克隆抗体12CA5和抗原表位标记的功能性Kar1p进行的免疫电子显微镜研究表明,Kar1p与纺锤体的半桥或半桥相关。 Cdc31p,一种Ca(2+)结合蛋白,以前被确定为纺锤极体半桥的第一部分(Spang,A.,I. Courtney,U. Fackler,M. Matzner和E. Schiebel 1993.J.Cell Biol.123:405-416)。使用体外分析,我们证明了Cdc31p与Kar1p羧基末端一半内的短序列特异性相互作用。 Kar1p的潜在Cdc31p结合序列包含钙调蛋白结合肽中未发现的三个酸性氨基酸,这解释了Cdc31p和钙调蛋白的不同底物特异性。 Cdc31p还能够结合SPB的另一种组分Nuflp / Spc110p的羧基末端(Kilmartin,J.V.,S.L.Dyos,D.Kershaw,和J.T.Finch.1993.J.Cell Biol.123:1175-1184)。 Kar1p与主轴极体的关联独立于Cdc31p。另一方面,Cdc31p与kar1细胞的SPB无关。

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