Skibbens R V, Skeen V P, Salmon E D
Department of Biology, University of North Carolina, Chapel Hill 27599-3280.
J Cell Biol. 1993 Aug;122(4):859-75. doi: 10.1083/jcb.122.4.859.
Most models of mitotic congression and segregation assume that only poleward pulling forces occur at kinetochores. However, there are reports for several different cell types that both mono-oriented and bi-oriented chromosomes oscillate toward and away from the pole throughout mitosis. We used new methods of high resolution video microscopy and computer-assisted tracking techniques to measure the positions over time of individual kinetochores with respect to their poles during mitosis in living newt lung cells. The results show that kinetochores oscillate throughout mitosis when they are tethered to spindle poles by attachment to the plus-ends of kinetochore microtubules (kMTs). Oscillations were not sinusoidal. Instead, kinetochores abruptly (as quick as 6 s or less) switched between persistent (approximately 1.5 min average duration) phases of poleward (P) and away from the pole (AP) movement. This kinetochore "directional instability" was a property of motility at the plus-ends of kMTs since fluorescent marks on the lattice of kMTs have previously been observed to exhibit only relatively slow P movement. Each P and AP phase consisted of one or a few constant velocity domains (approximately 1.7 microns/min average velocity). Velocities of P and AP phases were similar from prometaphase through mid-anaphase. Kinetochores occasionally switched to an indeterminant (N) phase of no or confused motion, which was usually brief compared to the durations of P and AP phases. Net chromosome displacements that occurred during congression to the equator or poleward movement during anaphase were primarily generated by differences in the durations and not the velocities of P and AP movements. Careful analysis of centromere deformation showed that kinetochore P movement produced pulling forces while kinetochore AP movement produced pushing forces. These data show that kinetochore directional instability is fundamental to the processes of chromosome congression and segregation. We argue that tension at the kinetochore attachment site is a key factor which controls the switching between P and AP phases of kinetochore motion.
大多数有丝分裂汇聚和分离模型都假定,动粒处仅存在向极拉力。然而,有针对几种不同细胞类型的报道称,单极定向和双极定向的染色体在整个有丝分裂过程中都会朝着和远离纺锤体极振荡。我们运用高分辨率视频显微镜新技术和计算机辅助追踪技术,来测量活体蝾螈肺细胞有丝分裂期间单个动粒相对于其纺锤体极随时间的位置。结果表明,当动粒通过附着于动粒微管(kMT)的正端而与纺锤体极相连时,它们在整个有丝分裂过程中都会振荡。振荡并非正弦波形式。相反,动粒在向极(P)和远离极(AP)运动的持续(平均持续时间约1.5分钟)阶段之间突然(快至6秒或更短时间)切换。这种动粒“方向不稳定性”是kMT正端运动性的一种特性,因为此前观察到kMT晶格上的荧光标记仅表现出相对缓慢的向极运动。每个P和AP阶段都由一个或几个恒定速度域组成(平均速度约为1.7微米/分钟)。从前中期到中期后期,P和AP阶段的速度相似。动粒偶尔会切换到无运动或运动混乱的不确定(N)阶段,与P和AP阶段的持续时间相比,该阶段通常很短暂。在向赤道汇聚或后期向极运动期间发生的净染色体位移,主要是由P和AP运动的持续时间差异而非速度差异产生的。对着丝粒变形的仔细分析表明,动粒P运动产生拉力,而动粒AP运动产生推力。这些数据表明,动粒方向不稳定性是染色体汇聚和分离过程的基础。我们认为,动粒附着位点的张力是控制动粒运动P和AP阶段之间切换的关键因素。