Julian M, Tollon Y, Lajoie-Mazenc I, Moisand A, Mazarguil H, Puget A, Wright M
Laboratoire de Pharmacologie et de Toxicologie fondamentales, CNRS, Toulouse, France.
J Cell Sci. 1993 May;105 ( Pt 1):145-56. doi: 10.1242/jcs.105.1.145.
Animal cells undergoing cytokinesis form an inter-cellular bridge containing two bundles of microtubules interdigitated at their plus ends, which constitute the midbody. Polyclonal antibodies raised against three specific amino acid sequences of gamma-tubulin (EEFATEGGDRKDV, NIIQGEADPTDVHKSL and EYHAATRPDYISWGTQEQ) specifically stained the centrosome in interphase, the spindle poles in all stages of mitosis, and the extremities of the midbody in mammalian cells (Potorous, human, Chinese hamster, mouse). This staining was prevented by the corresponding peptides, by Xenopus gamma-tubulin, but was not modified by purified alpha beta-tubulin heterodimer. An identical staining was obtained with affinity-purified antibodies against the carboxyl-terminal amino acid sequence of human gamma-tubulin. No gamma-tubulin could be detected in the interzone during anaphase and early telophase. Material containing gamma-tubulin first appeared in the two daughter cells on each side of the division plane in late telophase, and accumulated transiently at the minus ends of the two microtubule bundles constituting the midbody for one hour after metaphase. Micro-injection of gamma-tubulin antibodies into anaphase cells prevented the subsequent formation of the microtubule bundles between the two daughter cells. In contrast with previous views, these observations suggest that the microtubules constituting the midbody may be nucleated on special microtubule organizing centres, active during late telophase only, and assembled on each side of the dividing plane between the daughter cells.
正在进行胞质分裂的动物细胞会形成一个细胞间桥,其中包含两束在正端相互交错的微管,这些微管构成了中间体。针对γ-微管蛋白的三个特定氨基酸序列(EEFATEGGDRKDV、NIIQGEADPTDVHKSL和EYHAATRPDYISWGTQEQ)产生的多克隆抗体,能特异性地对间期的中心体、有丝分裂各阶段的纺锤体极以及哺乳动物细胞(袋鼠、人类、中国仓鼠、小鼠)中间体的末端进行染色。这种染色会被相应的肽、非洲爪蟾γ-微管蛋白阻止,但不会被纯化的αβ-微管蛋白异二聚体改变。用针对人类γ-微管蛋白羧基末端氨基酸序列的亲和纯化抗体也能得到相同的染色结果。在后期和早末期的中间区域未检测到γ-微管蛋白。含有γ-微管蛋白的物质在末期后期首次出现在分裂平面两侧的两个子细胞中,并在中期后一小时内短暂积累在构成中间体的两束微管的负端。将γ-微管蛋白抗体显微注射到后期细胞中会阻止两个子细胞之间随后形成微管束。与之前的观点相反,这些观察结果表明,构成中间体的微管可能在特殊的微管组织中心上成核,仅在末期后期活跃,并在子细胞之间分裂平面的每一侧组装。