Centrin is a conserved protein that forms diverse associations with centrioles and MTOCs in Naegleria and other organisms.

Y Y Levy, E Y Lai, S P Remillard, M B Heintzelman, C Fulton
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引用次数: 127

Abstract

Centrin, a approximately or equal to 20 kDa calcium-binding protein also known as caltractin, is a component of centrosome-associated algal flagellar roots capable of calcium-mediated contraction, and is also found in the centrosomes of vertebrate cells. Our analysis of a centrin gene from a protist, the amoeboflagellate Naegleria gruberi, reveals conserved features that distinguish centrins from calmodulin. Antibodies to bacterially expressed Naegleria centrin, which also recognize yeast Cdc31p, were employed to localize centrin immunoreactivity in selected organisms possessing specialized microtubule-organizing centers (MTOCs) or accessory structures. There is a striking morphological diversity of such structures. In the simplest associations, as found in Naegleria flagellates and vertebrates tracheal epithelium, centrin is intimately associated with the cylinder of the basal bodies. In cells with unfocused mitotic spindles, Naegleria amoebae and onion root tips, no localization of centrin was detected. In Dictyostelium discoideum and Saccharomyces cerevisiae, which lack centrioles, centrin immunoreactivity was observed as punctate cytoplasmic bodies but not associated with spindle pole MTOCs. In Paramecium multimicronucleatum, centrin immunoreactivity is localized to the infraciliary lattice, previously shown to exhibit calcium-mediated contraction. In Vorticella microstoma, known for the calcium-induced rapid contraction of its stalk, centrin immunoreactivity is localized to the contractile spasmoneme and myonemes. Similar antigens from Paramecium and Vorticella are detected by anti-centrin and anti-spasmin. The pattern of localization of centrin immunoreactivity supports the conjecture that a contractile system involving centrin, initially associated with centriolar structures, was recruited during evolution to build specialized organelles in different organisms and cell types.

中心蛋白是一种保守蛋白,在奈格里亚和其他生物中与中心粒和mtoc形成多种关联。
中心蛋白是一种大约等于20 kDa的钙结合蛋白,也被称为caltractin,是中心体相关藻鞭毛根的一种成分,能够钙介导的收缩,也存在于脊椎动物细胞的中心体中。我们对原生生物(变形虫鞭毛虫格鲁伯氏Naegleria gruberi)的中心蛋白基因进行了分析,揭示了区分中心蛋白和钙调蛋白的保守特征。研究人员利用细菌表达的中心耐格氏杆菌抗体(也能识别酵母Cdc31p),在具有特化微管组织中心(MTOCs)或附属结构的特定生物体中定位中心蛋白的免疫反应性。这类结构在形态上有着惊人的多样性。在最简单的联系中,如鞭毛虫和脊椎动物的气管上皮,中心蛋白与基底体的圆柱体密切相关。在有丝分裂纺锤体未聚焦的细胞中,变形虫奈格勒氏菌和洋葱根尖未检测到中心蛋白的定位。在缺少中心粒的盘状盘状钢和酿酒酵母中,中心蛋白的免疫反应表现为点状细胞质体,但与纺锤极MTOCs无关。在多微核草履虫中,中心蛋白的免疫反应性局限于纤毛下晶格,先前显示出钙介导的收缩。在以钙诱导其茎部快速收缩而闻名的小气孔Vorticella microstoma中,中心蛋白的免疫反应性局限于可收缩的痉挛素和肌素。用抗中心蛋白和抗痉挛蛋白检测草履虫和Vorticella的相似抗原。中心蛋白免疫反应性的定位模式支持了一种猜想,即一个涉及中心蛋白的收缩系统,最初与中心粒结构有关,在进化过程中被招募,在不同的生物体和细胞类型中建立专门的细胞器。
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