Davidson L, LaFountain J R
Biosystems. 1975 Nov;7(3-4):326-36. doi: 10.1016/0303-2647(75)90010-6.
The micronuclear mitotic spindle of Tetrahymena pyriformis contains several distinctive elements. The 150 or so continuous microtubules (MTs) form a peripheral sheath just inside the inner nuclear membrane while the kinetochore bundles traverse the center of the nucleoplasm. A new set of microtubules, the separation spindle, appears during the 10-fold nuclear elongation which occurs during the late anaphase. Both the separation spindle and peripheral sheath MTs are present in the macronucleus during macronuclear division but there are no definite kinetochore MTs. In the cresent stage of meiotic prophase both peripheral sheath and kinetochore MTs are present in the micronucleus. By using our own, and other workers', data in conjunction with the phylogenetic scheme for the ciliates which has been designed by Corliss (1974, 1975), we have attempted to trace out the evolutionary history of the various elements of the ciliate mitotic spindle. For example, the micronuclear separation spindle can be followed, from its point of origin within the primitive gymnostomes, throughout the phylum. The separation spindle of the macronucleus, by contrast, is lost at the level of the heterotrichs. Similarly, the anaphase breakdown and reconstitution of the nuclear envelope, which occurs in the primitive Loxodes magnus, can be followed up some phyletic branches, such as the heterotrichs, but in the suctorians and some other groups this feature seems to have been lost. Tracing the evolution of the ciliate mitotic spindle is made very difficult both by the incompleteness of the data and by what appear to be a number of cases of secondary reduction and parallel evolution. In general, however, the evolution of mitosis correlates well with the phylogeny of the ciliates constructed by Corliss and we consider this an independent substantiation of the general correctness of his phylogeny.
梨形四膜虫的微核有丝分裂纺锤体包含几个独特的成分。大约150根连续的微管形成了一个位于内核膜内侧的外周鞘,而动粒束则穿过核质中心。一组新的微管,即分离纺锤体,出现在后期末发生的10倍核伸长过程中。分离纺锤体和外周鞘微管在大核分裂期间都存在于大核中,但没有明确的动粒微管。在减数分裂前期的新月阶段,外周鞘和动粒微管都存在于微核中。通过结合我们自己以及其他研究者的数据,以及科利斯(1974年、1975年)设计的纤毛虫系统发育方案,我们试图追溯纤毛虫有丝分裂纺锤体各成分的进化历史。例如,微核分离纺锤体可以从其在原始裸口类中的起源点开始,在整个门中追踪。相比之下,大核的分离纺锤体在异毛类水平上消失了。同样,在原始的大斜管虫中发生的核膜后期解体和重建,可以在一些系统发育分支中追踪,比如异毛类,但在吸管虫类和其他一些类群中,这个特征似乎已经消失了。由于数据的不完整性以及似乎存在的一些次生简化和平行进化的情况,追踪纤毛虫有丝分裂纺锤体的进化变得非常困难。然而,一般来说,有丝分裂的进化与科利斯构建的纤毛虫系统发育密切相关,我们认为这是对他的系统发育总体正确性的一个独立证实。