Ferraro-Gideon Jessica, Hoang Carina, Forer Arthur
Department of Biology, York University, 4700 Keele St, Toronto, ON, M3J 1P3, Canada,
Protoplasma. 2014 Jan;251(1):127-43. doi: 10.1007/s00709-013-0532-9. Epub 2013 Aug 7.
In this article, we describe meiosis-I in spermatocytes of the free-living freshwater flatworm Mesostoma ehrenbergii. The original observations of Oakley (1983, 1985) and Fuge (Eur J Cell Biol 44:294-298, 1987, Cell Motil Cytoskeleton 13:212-220, 1989, Protoplasma 160:39-48, 1991), the first to describe these cells, challenge our understanding of cell division, and we have expanded on these descriptions with the aim of laying the framework for further experimental work. These cells contain three bivalents and four univalent chromosomes (two pairs). Bivalent kinetochores oscillate vigorously and regularly throughout prometaphase, for up to several hours, until anaphase. Anaphase onset usually begins in the middle of the kinetochore oscillation cycle. Precocious cleavage furrows form at the start of prometaphase, ingress and then remain arrested until the end of anaphase. The four univalents do not pair, yet by anaphase there is one of each kind at each pole, an example of "distance segregation" (Hughes-Schrader in Chromosoma 27:109-129, 1969). Until proper segregation is achieved, univalents move between spindle poles up to seven times in an individual cell; they move with velocities averaging 9 μm/min, which is faster than the oscillatory motions of the bivalent kinetochores (5-6 μm/min), and much faster than the anaphase movements of the segregating half-bivalents (1 μm/min). Bipolar bivalents periodically reorient, most often resulting in the partner kinetochores exchanging poles. We suggest that the large numbers of inter-polar movements of univalents, and the reorientations of bivalents that lead to partners exchanging poles, might be because there is non-random segregation of chromosomes, as in some other cell types.
在本文中,我们描述了自由生活的淡水扁虫埃氏中口涡虫精母细胞中的减数分裂I。奥克利(1983年、1985年)和富格(《欧洲细胞生物学杂志》44:294 - 298,1987年;《细胞运动与细胞骨架》13:212 - 220,1989年;《原生质体》160:39 - 48,1991年)最早描述了这些细胞,他们的原始观察结果挑战了我们对细胞分裂的理解,我们在此基础上进行了扩展描述,旨在为进一步的实验工作奠定框架。这些细胞含有三条二价体和四条单价染色体(两对)。二价体的动粒在整个前中期剧烈且有规律地振荡,长达数小时,直至后期。后期开始通常发生在动粒振荡周期的中期。早熟的分裂沟在前中期开始时形成,向内凹陷,然后一直停滞到后期结束。四条单价体不配对,但到后期时,每种单价体的一条在每个极,这是“距离分离”的一个例子(休斯 - 施拉德,《染色体》27:109 - 129,1969年)。在实现正确分离之前,单价体在单个细胞中在纺锤体两极之间移动多达七次;它们移动的平均速度为9μm/分钟,这比二价体动粒的振荡运动速度(5 - 6μm/分钟)快,比分离的半二价体的后期运动速度(1μm/分钟)快得多。双极二价体周期性地重新定向,最常见的结果是配对的动粒交换两极。我们认为,单价体大量的极间移动以及导致配对动粒交换两极的二价体重新定向,可能是因为存在染色体的非随机分离,就像在其他一些细胞类型中一样。