首页> 美国卫生研究院文献>The Journal of Biophysical and Biochemical Cytology >Microtubule dynamics investigated by microinjection of Paramecium axonemal tubulin: lack of nucleation but proximal assembly of microtubules at the kinetochore during prometaphase
【2h】

Microtubule dynamics investigated by microinjection of Paramecium axonemal tubulin: lack of nucleation but proximal assembly of microtubules at the kinetochore during prometaphase

机译:通过显微注射草履虫轴索微管蛋白研究的微管动力学:缺乏成核但在前中期在动粒体近端组装了微管

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Microtubule (MT) dynamics in PtK2 cells have been investigated using in vivo injection of unmodified Paramecium ciliary tubulin and time-lapse fixation. The sites of incorporation of the axonemal tubulin were localized using a specific antibody which does not react with vertebrate cytoplasmic tubulin (Adoutte, A., M. Claisse, R. Maunoury, and J. Beisson. 1985. J. Mol. Evol. 22:220-229), followed by immunogold labeling, Nanovid microscopy, and ultrastructural observation of the same cells. We confirm data from microinjection of labeled tubulins in other cell types (Soltys, B. J., and G. G. Borisy. 1985. J. Cell Biol. 100:1682-1689; Mitchison, T., L. Evans, E. Schulze, and M. Kirschner. 1986. Cell. 45:515-527; Schulze, E., and M. Kirschner. 1986. J. Cell Biol. 102:1020-1031). In agreement with the dynamic instability model (Mitchison, T., and M. Kirschner. 1984. Nature (Lond.). 312:237-242), during interphase, fast (2.6 microns/min) distal growth of MTs occurs, together with new centrosomal nucleation. Most of the cytoplasmic MT complex is replaced within 15-30 min. During mitosis, astral MTs display the same pattern of renewal, but the turnover of the MT system is much faster (approximately 6 min). We have concentrated on the construction of the kinetochore fibers during prometaphase and observe that (a) incorporation of tubulin in the vicinity of the kinetochores is not seen during prophase and early prometaphase as long as the kinetochores are not yet connected to a pole by MTs; (b) proximal time- dependent incorporation occurs only into preexisting kinetochore MTs emanating from centrosomes. Consequently, in undisturbed prometaphase cells, the kinetochores probably do not act as independent nucleation sites. This confirms a model in which, at prometaphase, fast probing centrosomal MTs are grabbed by the kinetochores, where tubulin incorporation then takes place.
机译:使用未经修饰的草履虫纤毛纤毛蛋白的体内注射和延时固定,已经研究了PtK2细胞中的微管(MT)动力学。使用不与脊椎动物细胞质微管蛋白反应的特异性抗体定位轴突微管蛋白的结合位点(Adoutte,A.,M. Claisse,R. Maunoury,and J.Beisson。1985. J. Mol。Evol.22 :220-229),然后进行免疫金标记,Nanovid显微镜检查和相同细胞的超微结构观察。我们证实了在其他细胞类型(Soltys,BJ和GG Borisy.1985.J.Cell Biol.100:1682-1689; Mitchison,T.,L.Evans,E.Schulze和M. Kirschner.1986.Cell.45:515-527; Schulze,E。和M.Kirschner.1986.J.Cell Biol.102:1020-1031)。与动态不稳定性模型相一致(Mitchison,T.和M. Kirschner。1984. Nature(Lond。)。312:237-242),在相间期,MT发生了快速(2.6微米/分钟)的远端生长新的中心体成核。大多数细胞质MT复合物在15-30分钟内被替换。在有丝分裂期间,星体MT会显示相同的更新模式,但是MT系统的更新速度要快得多(大约6分钟)。我们集中研究了前中期动粒纤维的构造,并观察到:(a)在前阶段和前中期早期,只要动植物尚未通过MT连接到极,就不会在微管蛋白附近掺入微管蛋白。 (b)近端时间依赖性掺入仅发生于由中心体发出的既往动粒MT中。因此,在未受干扰的前中期细胞中,动植物可能不充当独立的成核位点。这证实了一种模型,其中在前期,快速探测中心体MT被动植物捕获,然后发生微管蛋白掺入。

著录项

相似文献

  • 外文文献
  • 中文文献
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号