Roos U P
Chromosoma. 1976 Mar 10;54(4):363-85. doi: 10.1007/BF00292816.
Chromosome orientation and behavior during prometaphase of mitosis in PtK1 rat kangaroo cells were investigated by cinémicrography and electron microscopy. The first chromosome movements occur soon after the nuclear envelope begins to break down in the region near each pole. Initial chromosome behavior is primarily determined by the distance from the kinetochore region to the spindle poles. The predominant pattern is a movement to and/or association with the proximal pole. Movement to and association with the more distant pole, or direct alignment at or near the spindle equator (direct congression) are less frequent patterns. Except for rare cases, pole-associated chromosomes congress sooner or later and most congressed chromosomes oscillate about the equator.--Ultrastructural observations suggest that pole-associated chromosomes are oriented only to the poximal pole (monotelic or syntelic orientation) and they demonstrate that the sister-kinetochores of congressing or oscillating chromosomes are oriented to opposite poles (amphitelic orientation).--Based on the structure of the early prometaphase spindle and four assumptions concerning the formation of kinetochore fibers and their force-producing interaction with complementary elements, the different patterns of chromosome behavior observed can be explained as a result of synchronous or asynchronous formation of sister-kinetochore fibers. The few chromosomes whose kinetochore region is approximately equidistant from the poles amphi-orient immediately because their sister-kinetochores form fibers synchronously and they congress directly because of the bidirectional forces to which they are subjected. The kinetochore region of most chromosomes is not equidistant from the poles. Therefore, they form a functional fiber first to the nearer pole and move to, or associate with it, it because of the unidirectional force. Eventually, however, these chromosomes achieve amphitelic orientation and congress. Once established, amphitelic orientation is stable. Re-orientations do not occur during congression or oscillatory movements.
利用电影显微摄影术和电子显微镜,对PtK1大鼠袋鼠细胞有丝分裂前中期的染色体取向和行为进行了研究。在每个极附近的区域,核膜开始解体后不久,染色体就开始了首次移动。初始染色体行为主要由着丝粒区域到纺锤体极的距离决定。主要模式是向近端极移动和/或与近端极结合。向较远极移动并与其结合,或在纺锤体赤道处或附近直接排列(直接汇聚)的模式则较少见。除了极少数情况外,与极相关的染色体迟早会汇聚,并且大多数汇聚的染色体在赤道附近振荡。超微结构观察表明,与极相关的染色体仅向近端极取向(单着丝粒或同着丝粒取向),并且它们表明正在汇聚或振荡的染色体的姐妹着丝粒向相反的极取向(双着丝粒取向)。基于有丝分裂前早期纺锤体的结构以及关于着丝粒纤维形成及其与互补元件产生力的相互作用的四个假设,观察到的不同染色体行为模式可以解释为姐妹着丝粒纤维同步或异步形成的结果。少数着丝粒区域与两极距离大致相等的染色体立即进行双取向,因为它们的姐妹着丝粒同步形成纤维,并且由于它们受到双向力的作用而直接汇聚。大多数染色体的着丝粒区域与两极的距离不相等。因此,它们首先形成一条功能性纤维连接到较近的极,并由于单向力而向该极移动或与之结合。然而,最终这些染色体实现双着丝粒取向并汇聚。一旦确立,双着丝粒取向就是稳定的。在汇聚或振荡运动期间不会发生重新取向。