Rieder C L, Alexander S P
Wadsworth Center for Laboratories and Research, Albany, New York 12201-0509.
J Cell Biol. 1990 Jan;110(1):81-95. doi: 10.1083/jcb.110.1.81.
During mitosis in cultured newt pneumocytes, one or more chromosomes may become positioned well removed (greater than 50 microns) from the polar regions during early prometaphase. As a result, these chromosomes are delayed for up to 5 h in forming an attachment to the spindle. The spatial separation of these chromosomes from the polar microtubule-nucleating centers provides a unique opportunity to study the initial stages of kinetochore fiber formation in living cells. Time-lapse Nomarski-differential interference contrast videomicroscopic observations reveal that late-attaching chromosomes always move, upon attachment, into a single polar region (usually the one closest to the chromosome). During this attachment, the kinetochore region of the chromosome undergoes a variable number of transient poleward tugs that are followed, shortly thereafter, by rapid movement of the chromosome towards the pole. Anti-tubulin immunofluorescence and serial section EM reveal that the kinetochores and kinetochore regions of nonattached chromosomes lack associated microtubules. By contrast, these methods reveal that the attachment and subsequent poleward movement of a chromosome correlates with the association of a single long microtubule with one of the kinetochores of the chromosome. This microtubule traverses the entire distance between the spindle pole and the kinetochore and often extends well past the kinetochore. From these results, we conclude that the initial attachment of a chromosome to the newt pneumocyte spindle results from an interaction between a single polar-nucleated microtubule and one of the kinetochores on the chromosome. Once this association is established, the kinetochore is rapidly transported poleward along the surface of the microtubule by a mechanism that is not dependent on microtubule depolymerization. Our results further demonstrate that the motors for prometaphase chromosome movement must be either on the surface of the kinetochore (i.e., within the corona but not the plate), distributed along the surface of the kinetochore microtubules, or both.
在培养的蝾螈肺细胞有丝分裂过程中,在早前期,一条或多条染色体可能会定位在远离极区(超过50微米)的位置。因此,这些染色体在形成与纺锤体的附着方面会延迟长达5小时。这些染色体与极微管成核中心的空间分离为研究活细胞中动粒纤维形成的初始阶段提供了独特的机会。延时相差干涉对比视频显微镜观察显示,晚附着的染色体在附着后总是会移动到单个极区(通常是最靠近染色体的那个极区)。在这个附着过程中,染色体的动粒区域会经历数量不等的短暂向极牵拉,随后不久,染色体就会迅速向极移动。抗微管蛋白免疫荧光和连续切片电镜显示,未附着染色体的动粒和动粒区域缺乏相关微管。相比之下,这些方法显示染色体的附着及随后的向极移动与一条单个的长微管与染色体的一个动粒的结合相关。这条微管横跨纺锤体极与动粒之间的整个距离,并且常常延伸到动粒之外。从这些结果我们得出结论,染色体与蝾螈肺细胞纺锤体的初始附着是由单个极成核微管与染色体上的一个动粒之间的相互作用导致的。一旦这种结合建立,动粒就会通过一种不依赖微管解聚的机制沿着微管表面迅速向极运输。我们的结果进一步证明,早前期染色体运动的马达必定要么在动粒表面(即在内冠而非板层内),要么沿动粒微管表面分布,要么两者皆有。