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秀丽隐杆线虫中心粒形成过程中的顺序性蛋白质招募

Sequential protein recruitment in C. elegans centriole formation.

作者信息

Delattre Marie, Canard Coralie, Gönczy Pierre

机构信息

Swiss Institute for Experimental Cancer Research, School of Life Sciences (ISREC), Swiss Federal Institute of Technology (EPFL), Lausanne, Switzerland.

出版信息

Curr Biol. 2006 Sep 19;16(18):1844-9. doi: 10.1016/j.cub.2006.07.059.

Abstract

Formation of the microtubule-based centriole is a poorly understood process that is crucial for duplication of the centrosome, the principal microtubule-organizing center of animal cells . Five proteins have been identified as being essential for centriole formation in Caenorhabditis elegans: the kinase ZYG-1, as well as the coiled-coil proteins SAS-4, SAS-5, SAS-6, and SPD-2 . The relationship between these proteins is incompletely understood, limiting understanding of how they contribute to centriole formation. In this study, we established the order in which these five proteins are recruited to centrioles, and we conducted molecular epistasis experiments expanding on earlier work. We find that SPD-2 is loaded first and is needed for the centriolar localization of the four other proteins. ZYG-1 recruitment is required thereafter for the remaining three proteins to localize to centrioles. SAS-5 and SAS-6 are recruited next and are needed for the presence of SAS-4, which is incorporated last. Our results indicate in addition that the presence of SAS-5 and SAS-6 allows diminution of centriolar ZYG-1. Moreover, astral microtubules appear dispensable for the centriolar recruitment of all five proteins. Several of these proteins have homologs in other metazoans, and we expect the assembly pathway that stems from our work to be conserved.

摘要

基于微管的中心粒形成是一个尚未完全理解的过程,对中心体(动物细胞主要的微管组织中心)的复制至关重要。已鉴定出五种蛋白质对线虫中心粒形成必不可少:激酶ZYG-1以及卷曲螺旋蛋白SAS-4、SAS-5、SAS-6和SPD-2。这些蛋白质之间的关系尚未完全了解,限制了我们对它们如何促进中心粒形成的理解。在本研究中,我们确定了这五种蛋白质被招募到中心粒的顺序,并进行了分子上位性实验,扩展了早期的研究工作。我们发现SPD-2首先被加载,并且是其他四种蛋白质在中心粒定位所必需的。此后,ZYG-1的招募是其余三种蛋白质定位于中心粒所必需的。接下来招募SAS-5和SAS-6,它们是SAS-4存在所必需的,而SAS-4是最后整合的。我们的结果还表明,SAS-5和SAS-6的存在会使中心粒中的ZYG-1减少。此外,星状微管似乎对所有五种蛋白质的中心粒招募都是可有可无的。这些蛋白质中的几种在其他后生动物中有同源物,我们预计源自我们工作的组装途径是保守的。

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