Wolniak S M, Larsen P M
Department of Botany, University of Maryland, College Park 20742.
J Cell Sci. 1992 Aug;102 ( Pt 4):691-715. doi: 10.1242/jcs.102.4.691.
Stamen hair cells from the spiderwort plant, Tradescantia virginiana, exhibit remarkably predictable metaphase transit times, making them uniquely suitable for temporal studies on mitotic regulation. In this study, we describe two kinds of experiments that test whether protein phosphatase activity is a necessary prerequisite for entry into anaphase in living, mitotic cells. We treated cells at specific points during prophase, prometaphase and metaphase with the broad-spectrum protein phosphatase inhibitor, alpha-naphthyl phosphate (administered by microinjection), or with the naturally occurring, potent phosphatase inhibitors okadaic acid, microcystin-LR or microcystin-RR (administered by perfusion), and we have observed changes in the metaphase transit time that are primarily dependent on the time of initial exposure to the inhibitor. Maximal extensions of the metaphase transit time result from alpha-naphthyl phosphate microinjections initiated in mid-metaphase, 10-20 min after nuclear envelope breakdown. Perfusions with okadaic acid started during a specific interval in mid-metaphase, 15-20 min after nuclear envelope breakdown, resulted in a statistically significant extension of the metaphase transit time. Perfusions with either microcystin-LR or microcystin-RR initiated 15-26 min after nuclear envelope breakdown extended the metaphase transit times significantly. Treatments of cells with okadaic acid or with either of the microcystins initiated outside this mid-metaphase interval either were without effect or, alternatively, resulted in a significant shortening of the metaphase transit time. In addition to their effects on the timing of anaphase onset, treatments with these protein phosphatase inhibitors also resulted in a remarkable change in the way in which these cells enter anaphase. Sister chromatid separation in stamen hair cells typically requires only 5 seconds, but after treatment with any of these inhibitors some, but not all, of the chromatids split apart at anaphase onset. Those that split begin to migrate toward the spindle pole regions, while those that fail to split remain at the metaphase plate. Later, more of the paired chromatids split apart and begin moving toward the spindle pole regions. Those that fail to separate remain at the metaphase plate. This process can be repeated several times before all of the chromatids have separated. Thus, entry into anaphase becomes extremely asynchronous, and as much as 30 min can transpire between the centromeric separation of the first and last chromosomes. Some of the chromosomes complete their anaphase movements before others have even split apart at the metaphase plate. Asynchronous separation did not result in a permanent segregation anomaly.(ABSTRACT TRUNCATED AT 400 WORDS)
紫露草(Tradescantia virginiana)雄蕊毛细胞在中期的过渡时间具有显著的可预测性,这使得它们特别适合用于有丝分裂调控的时间研究。在本研究中,我们描述了两类实验,以测试蛋白磷酸酶活性是否是活的有丝分裂细胞进入后期的必要前提条件。我们在前期、前中期和中期的特定时间点,用广谱蛋白磷酸酶抑制剂α-萘基磷酸(通过显微注射给药),或用天然存在的强效磷酸酶抑制剂冈田酸、微囊藻毒素-LR或微囊藻毒素-RR(通过灌注给药)处理细胞,并观察到中期过渡时间的变化,这些变化主要取决于最初接触抑制剂的时间。从中期核膜破裂后10 - 20分钟开始显微注射α-萘基磷酸,会导致中期过渡时间的最大延长。在中期核膜破裂后15 - 20分钟的特定时间段开始用冈田酸灌注,会使中期过渡时间在统计学上显著延长。在核膜破裂后15 - 26分钟开始用微囊藻毒素-LR或微囊藻毒素-RR灌注,会显著延长中期过渡时间。在这个中期时间段之外开始用冈田酸或任何一种微囊藻毒素处理细胞,要么没有效果,要么会导致中期过渡时间显著缩短。除了对后期开始时间的影响外,用这些蛋白磷酸酶抑制剂处理还导致这些细胞进入后期的方式发生了显著变化。雄蕊毛细胞中的姐妹染色单体分离通常只需要5秒,但在用这些抑制剂中的任何一种处理后,一些(但不是全部)染色单体在后期开始时分开。那些分开的染色单体开始向纺锤极区域迁移,而那些未分开的染色单体则留在中期板上。后来,更多成对的染色单体分开并开始向纺锤极区域移动。那些未分开的染色单体留在中期板上。在所有染色单体都分离之前,这个过程可以重复几次。因此,进入后期变得极其不同步,第一条和最后一条染色体的着丝粒分离之间可能会经过长达30分钟的时间。一些染色体在其他染色体甚至还未在中期板上分开之前就完成了后期移动。不同步分离并未导致永久性的分离异常。(摘要截断于400字)