首页> 美国卫生研究院文献>The Journal of Biophysical and Biochemical Cytology >Cytoplasmic Dynein Is Required for Distinct Aspects of Mtoc Positioning Including Centrosome Separation in the One Cell Stage Caenorhabditis elegans Embryo
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Cytoplasmic Dynein Is Required for Distinct Aspects of Mtoc Positioning Including Centrosome Separation in the One Cell Stage Caenorhabditis elegans Embryo

机译:在一个细胞阶段秀丽隐杆线虫胚胎中Mtoc定位(包括中心体分离)的不同方面需要胞质动力蛋白

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摘要

We have investigated the role of cytoplasmic dynein in microtubule organizing center (MTOC) positioning using RNA-mediated interference (RNAi) in Caenorhabditis elegans to deplete the product of the dynein heavy chain gene dhc-1. Analysis with time-lapse differential interference contrast microscopy and indirect immunofluorescence revealed that pronuclear migration and centrosome separation failed in one cell stage dhc-1 (RNAi) embryos. These phenotypes were also observed when the dynactin components p50/dynamitin or p150Glued were depleted with RNAi. Moreover, in 15% of dhc-1 (RNAi) embryos, centrosomes failed to remain in proximity of the male pronucleus. When dynein heavy chain function was diminished only partially with RNAi, centrosome separation took place, but orientation of the mitotic spindle was defective. Therefore, cytoplasmic dynein is required for multiple aspects of MTOC positioning in the one cell stage C. elegans embryo. In conjunction with our observation of cytoplasmic dynein distribution at the periphery of nuclei, these results lead us to propose a mechanism in which cytoplasmic dynein anchored on the nucleus drives centrosome separation.
机译:我们已经研究了细胞质动力蛋白在秀丽隐杆线虫中使用RNA介导的干扰(RNAi)来消耗动力蛋白重链基因dhc-1的产物的微管组织中心(MTOC)定位中的作用。用时移微分干涉对比显微镜和间接免疫荧光分析显示,在一个细胞阶段dhc-1(RNAi)胚胎中,前核迁移和中心体分离失败。当动力蛋白p50 / dynamitin或p150 Glued 的RNAi耗尽时,也观察到了这些表型。此外,在15%的dhc-1(RNAi)胚胎中,中心体未能保留在雄性原核附近。当用RNAi仅使动力蛋白的重链功能部分减弱时,就会发生中心体分离,但是有丝分裂纺锤体的方向是有缺陷的。因此,在一个细胞阶段秀丽隐杆线虫胚胎中MTOC定位的多个方面都需要细胞质动力蛋白。结合我们对细胞核周围细胞质动力蛋白分布的观察,这些结果使我们提出了一种机制,其中锚定在细胞核上的细胞质动力蛋白驱动着中心体分离。

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