Khodjakov Alexey, Rieder Conly L, Sluder Greenfield, Cassels Grisel, Sibon Ody, Wang Chuo-Lung
Division of Molecular Medicine, Wadsworth Center, New York State Department of Health, Albany, NY 12201, USA.
J Cell Biol. 2002 Sep 30;158(7):1171-81. doi: 10.1083/jcb.200205102.
The centrosome usually replicates in a semiconservative fashion, i.e., new centrioles form in association with preexisting "maternal" centrioles. De novo formation of centrioles has been reported for a few highly specialized cell types but it has not been seen in vertebrate somatic cells. We find that when centrosomes are completely destroyed by laser microsurgery in CHO cells arrested in S phase by hydroxyurea, new centrosomes form by de novo assembly. Formation of new centrosomes occurs in two steps: approximately 5-8 h after ablation, clouds of pericentriolar material (PCM) containing gamma-tubulin and pericentrin appear in the cell. By 24 h, centrioles have formed inside of already well-developed PCM clouds. This de novo pathway leads to the formation of a random number of centrioles (2-14 per cell). Although clouds of PCM consistently form even when microtubules are completely disassembled by nocodazole, the centrioles are not assembled under these conditions.
中心体通常以半保留方式进行复制,即新的中心粒与预先存在的“母”中心粒相关联形成。虽然已经报道了少数高度特化的细胞类型中存在中心粒的从头形成,但在脊椎动物体细胞中尚未观察到。我们发现,当处于S期的CHO细胞被羟基脲阻滞,其中心体被激光显微手术完全破坏时,新的中心体通过从头组装形成。新中心体的形成分两步进行:消融后约5-8小时,含有γ-微管蛋白和中心体蛋白的中心粒周围物质(PCM)云出现在细胞中。到24小时时,中心粒已在发育良好的PCM云内部形成。这种从头途径导致形成随机数量的中心粒(每个细胞2-14个)。尽管即使微管被诺考达唑完全拆解,PCM云仍会持续形成,但在这些条件下中心粒不会组装。