Yu H G, Hiatt E N, Chan A, Sweeney M, Dawe R K
Department of Botany, University of Georgia, Athens, Georgia 30602, USA.
J Cell Biol. 1997 Nov 17;139(4):831-40. doi: 10.1083/jcb.139.4.831.
Neocentromere activity is a classic example of nonkinetochore chromosome movement. In maize, neocentromeres are induced by a gene or genes on Abnormal chromosome 10 (Ab10) which causes heterochromatic knobs to move poleward at meiotic anaphase. Here we describe experiments that test how neocentromere activity affects the function of linked centromere/kinetochores (kinetochores) and whether neocentromeres and kinetochores are mobilized on the spindle by the same mechanism. Using a newly developed system for observing meiotic chromosome congression and segregation in living maize cells, we show that neocentromeres are active from prometaphase through anaphase. During mid-anaphase, normal chromosomes move on the spindle at an average rate of 0.79 micron/min. The presence of Ab10 does not affect the rate of normal chromosome movement but propels neocentromeres poleward at rates as high as 1.4 micron/min. Kinetochore-mediated chromosome movement is only marginally affected by the activity of a linked neocentromere. Combined in situ hybridization/immunocytochemistry is used to demonstrate that unlike kinetochores, neocentromeres associate laterally with microtubules and that neocentromere movement is correlated with knob size. These data suggest that microtubule depolymerization is not required for neocentromere motility. We argue that neocentromeres are mobilized on microtubules by the activity of minus end-directed motor proteins that interact either directly or indirectly with knob DNA sequences.
新着丝粒活性是非着丝粒染色体运动的一个经典例子。在玉米中,新着丝粒由异常10号染色体(Ab10)上的一个或多个基因诱导产生,这些基因会导致异染色质结在减数分裂后期向两极移动。在此,我们描述了一些实验,以测试新着丝粒活性如何影响相连的着丝粒/动粒(动粒)的功能,以及新着丝粒和动粒是否通过相同机制在纺锤体上移动。利用一个新开发的系统来观察活的玉米细胞中的减数分裂染色体排列和分离,我们发现新着丝粒从前期到后期都是活跃的。在后期中期,正常染色体在纺锤体上以平均每分钟0.79微米的速度移动。Ab10的存在并不影响正常染色体的移动速度,但能以高达每分钟1.4微米的速度将新着丝粒推向两极。相连新着丝粒的活性对动粒介导的染色体运动仅有轻微影响。联合原位杂交/免疫细胞化学被用于证明,与动粒不同,新着丝粒与微管横向结合,并且新着丝粒的运动与结的大小相关。这些数据表明新着丝粒运动不需要微管解聚。我们认为,新着丝粒通过负端定向运动蛋白的活性在微管上移动,这些运动蛋白直接或间接与结DNA序列相互作用。