首页> 外文OA文献 >Caenorhabditis elegans ortholog of the p24/p22 subunit, DNC-3, is essential for the formation of the dynactin complex by bridging DNC-1/p150Glued and DNC-2/dynamitin
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Caenorhabditis elegans ortholog of the p24/p22 subunit, DNC-3, is essential for the formation of the dynactin complex by bridging DNC-1/p150Glued and DNC-2/dynamitin

机译:p24 / p22亚基的秀丽隐杆线虫直系同源物,通过桥接DNC-1 / p150胶粘剂和DNC-2 / dynamitin,对于形成肌动蛋白复合物至关重要

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摘要

Dynactin is a multisubunit protein complex required for the activity of cytoplasmic dynein. In Caenorhabditis elegans, although 10 of the 11 dynactin subunits were identified based on the sequence similarities to their orthologs, the p24/p22 subunit has not been detected in the genome. Here, we demonstrate that DNC-3 (W10G11.20) is the functional counterpart of the p24/p22 subunit in C. elegans. RNAi phenotypes and subcellular localization of DNC-3 in early C. elegans embryos were nearly identical to those of the known dynactin components. All other dynactin subunits were co-immunoprecipitated with DNC-3, indicating that DNC-3 is a core component of dynactin. Furthermore, the overall secondary structure of DNC-3 resembles to those of the mammalian and yeast p24/p22. We found that DNC-3 is required for the localization of the DNC-1/p150Glued and DNC-2/dynamitin, the two components of the projection arm of dynactin, to the nuclear envelope of meiotic nuclei in the adult gonad. Moreover, DNC-3 physically interacted with DNC-1 and DNC-2 and significantly enhanced the binding ability between DNC-1 and DNC-2 in vitro. These results suggest that DNC-3 is essential for the formation of the projection arm subcomplex of dynactin.
机译:Dynactin是细胞质Dynein活性所需的多亚基蛋白质复合物。在秀丽隐杆线虫中,尽管根据与它们的直向同源物的序列相似性鉴定了11个动力蛋白亚基中的10个,但在基因组中未检测到p24 / p22亚基。在这里,我们证明DNC-3(W10G11.20)是秀丽隐杆线虫p24 / p22亚基的功能对应物。线虫早期胚胎中DNC-3的RNAi表型和亚细胞定位与已知的dactactin组分几乎相同。所有其他动力蛋白亚基均与DNC-3共免疫沉淀,表明DNC-3是动力蛋白的核心成分。此外,DNC-3的总体二级结构类似于哺乳动物和酵母p24 / p22的二级结构。我们发现,DNC-1 / p150Glued和DNC-2 / dynamitin是Dynactin投射臂的两个组件,必须定位于成年性腺中减数分裂核的核膜。此外,DNC-3与DNC-1和DNC-2发生物理相互作用,并在体外显着增强了DNC-1和DNC-2之间的结合能力。这些结果表明,DNC-3对于动力蛋白的投射臂亚复合物的形成是必不可少的。

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