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Identification of a novel microtubule-associated protein that regulates microtubule organization and cytokinesis by using a GFP-screening strategy

机译:通过使用GFP筛选策略,鉴定一种新型的与微管相关的蛋白,该蛋白可调节微管的组织和胞质分裂

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Microtubules play critical roles in a variety of cell processes, including mitosis, organelle transport, adhesion and migration, and the maintenance of cell polarity [1-3]. Microtubule-associated proteins (MAPs) regulate the dynamic organization and stability of microtubules, often through either cell-specific or cell division stage-specific interactions [4, 5]. To identify novel cytoskeletal-associated proteins and peptides that regulate microtubules and other cytoskeletal and adhesive structures, we have developed a GFP cDNA screening strategy based on identifying gene products that localize to these structures. Using this approach, we have identified a novel MAP, GLFND, that shows homology to the Opitz syndrome gene product [6], localizes to a subpopulation of microtubules that are acetylated, and protects microtubules from depolymerization with nocodazole. Expression of an N-terminal deletion binds microtubules but alters their organization. During the cell cycle, GLFND dissociates from microtubules at the beginning of mitosis and then reassociates at cytokinesis. Furthermore, ectopic expression of GLFND inhibits cell division and cytokinesis in CHO cells. These observations make GLFND unique among MAPS characterized thus far.
机译:微管在多种细胞过程中起关键作用,包括有丝分裂,细胞器运输,粘附和迁移以及细胞极性的维持[1-3]。微管相关蛋白(MAPs)通常通过细胞特异性或细胞分裂阶段特异性相互作用来调节微管的动态组织和稳定性[4,5]。为了鉴定调节微管以及其他细胞骨架和粘附结构的新型细胞骨架相关蛋白和肽,我们基于鉴定定位于这些结构的基因产物,开发了一种GFP cDNA筛选策略。使用这种方法,我们已经鉴定出一种新型的MAP,GLFND,它显示出与Opitz综合征基因产物的同源性[6],定位于被乙酰化的微管亚群,并保护了微管免于与诺考达唑解聚。 N末端缺失的表达结合微管,但改变其组织。在细胞周期中,GLFND在有丝分裂开始时从微管解离,然后在胞质分裂时重新结合。此外,GLFND的异位表达抑制CHO细胞的细胞分裂和胞质分裂。这些观察结果使GLFND在迄今为止表征的MAPS中独树一帜。

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