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Interaction between the Caenorhabditis elegans centriolar protein SAS-5 and microtubules facilitates organelle assembly

机译:秀丽隐杆线虫中心蛋白SAS-5和微管之间的相互作用促进细胞器组装。

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Centrioles are microtubule-based organelles that organize the microtubule network and seed the formation of cilia and flagella. New centrioles assemble through a stepwise process dependent notably on the centriolar protein SAS-5 in Caenorhabditis elegans. SAS-5 and its functional homologues in other species form oligomers that bind the centriolar proteins SAS-6 and SAS-4, thereby forming an evolutionarily conserved structural core at the onset of organelle assembly. Here, we report a novel interaction of SAS-5 with microtubules. Microtubule binding requires SAS-5 oligomerization and a disordered protein segment that overlaps with the SAS-4 binding site. Combined in vitro and in vivo analysis of select mutants reveals that the SAS-5–microtubule interaction facilitates centriole assembly in C. elegans embryos. Our findings lead us to propose that the interdependence of SAS-5 oligomerization and microtubule binding reflects an avidity mechanism, which also strengthens SAS-5 associations with other centriole components and, thus, promotes organelle assembly.
机译:质心是基于微管的细胞器,可组织微管网络并播种纤毛和鞭毛的形成。新的中心粒通过逐步过程组装,该过程特别依赖于秀丽隐杆线虫中的中心粒蛋白SAS-5。 SAS-5及其在其他物种中的功能同源物形成与中心粒蛋白SAS-6和SAS-4结合的寡聚体,从而在细胞器组装开始时形成进化上保守的结构核心。在这里,我们报告SAS-5与微管的新型相互作用。微管结合需要SAS-5寡聚化和与SAS-4结合位点重叠的无序蛋白片段。结合体外和体内选择的突变体分析发现,SAS-5-微管相互作用促进秀丽隐杆线虫胚胎的中心体组装。我们的发现使我们提出SAS-5寡聚和微管结合的相互依赖性反映了一种亲和力机制,该机制也增强了SAS-5与其他中心体成分的结合,从而促进了细胞器的组装。

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