Zhou Kang, Rolls Melissa M, Hall David H, Malone Christian J, Hanna-Rose Wendy
Department of Biochemistry and Molecular Biology, The Pennsylvania State University, University Park, PA 16802, USA.
J Cell Biol. 2009 Jul 27;186(2):229-41. doi: 10.1083/jcb.200902101.
Changes in cellular microtubule organization often accompany developmental progression. In the Caenorhabditis elegans embryo, the centrosome, which is attached to the nucleus via ZYG-12, organizes the microtubule network. In this study, we investigate ZYG-12 function and microtubule organization before embryo formation in the gonad. Surprisingly, ZYG-12 is dispensable for centrosome attachment in the germline. However, ZYG-12-mediated recruitment of dynein to the nuclear envelope is required to maintain microtubule organization, membrane architecture, and nuclear positioning within the syncytial gonad. We examined gamma-tubulin localization and microtubule regrowth after depolymerization to identify sites of nucleation in germ cells. gamma-Tubulin localizes to the plasma membrane in addition to the centrosome, and regrowth initiates at both sites. Because we do not observe organized microtubules around zyg-12(ct350) mutant nuclei with attached centrosomes, we propose that gonad architecture, including membrane and nuclear positioning, is determined by microtubule nucleation at the plasma membrane combined with tension on the microtubules by dynein anchored at the nucleus by ZYG-12.
细胞微管组织的变化常常伴随着发育进程。在秀丽隐杆线虫胚胎中,通过ZYG-12与细胞核相连的中心体组织微管网络。在本研究中,我们调查了性腺中胚胎形成前ZYG-12的功能和微管组织。令人惊讶的是,ZYG-12对于生殖系中的中心体附着是可有可无的。然而,需要ZYG-12介导的动力蛋白募集到核膜来维持微管组织、膜结构以及合胞性腺内的核定位。我们检查了γ-微管蛋白的定位以及解聚后微管的重新生长,以确定生殖细胞中的成核位点。除了中心体,γ-微管蛋白还定位于质膜,并且重新生长在这两个位点都起始。因为我们在带有附着中心体的zyg-12(ct350)突变核周围未观察到有组织的微管,所以我们提出,性腺结构,包括膜和核定位,是由质膜处的微管成核以及由ZYG-12锚定在核上的动力蛋白对微管施加的张力共同决定的。