Savoian Matthew S
Massey University, Institute of Fundamental Sciences, Palmerston North, New Zealand.
J Biomol Tech. 2015 Jul;26(2):66-73. doi: 10.7171/jbt.15-2602-004.
In dividing animal cells, a microtubule (MT)-based bipolar spindle governs chromosome movement. Current models propose that the spindle facilitates and/or generates translocating forces by regionally depolymerizing the kinetochore fibers (k-fibers) that bind each chromosome. It is unclear how conserved these sites and the resultant chromosome-moving mechanisms are between different dividing cell types because of the technical challenges of quantitatively studying MTs in many specimens. In particular, our knowledge of MT kinetics during the sperm-producing male meiotic divisions remains in its infancy. In this study, I use an easy-to-implement photobleaching-based assay for measuring spindle MT dynamics in primary cultures of meiotic spermatocytes isolated from the fruit fly Drosophila melanogaster. By use of standard scanning confocal microscopy features, fiducial marks were photobleached on fluorescent protein (FP)-tagged MTs. These were followed by time-lapse imaging during different division stages, and their displacement rates were calculated using public domain software. I find that k-fibers continually shorten at their poles during metaphase and anaphase A through the process of MT flux. Anaphase chromosome movement is complemented by Pac-Man, the shortening of the k-fiber at its chromosomal interface. Thus, Drosophila spermatocytes share the sites of spindle dynamism and mechanisms of chromosome movement with mitotic cells. The data reveal the applicability of the photobleaching assay for measuring MT dynamics in primary cultures. This approach can be readily applied to other systems.
在动物细胞分裂过程中,基于微管(MT)的双极纺锤体控制染色体的移动。目前的模型认为,纺锤体通过局部解聚结合每条染色体的动粒纤维(k纤维)来促进和/或产生转运力。由于在许多标本中定量研究微管存在技术挑战,目前尚不清楚这些位点以及由此产生的染色体移动机制在不同分裂细胞类型之间的保守程度。特别是,我们对精子发生过程中雄性减数分裂期微管动力学的了解仍处于起步阶段。在本研究中,我使用了一种易于实施的基于光漂白的检测方法,来测量从果蝇中分离出的减数分裂期精母细胞原代培养物中纺锤体微管的动力学。利用标准的扫描共聚焦显微镜特性,在荧光蛋白(FP)标记的微管上对基准标记进行光漂白。随后在不同分裂阶段进行延时成像,并使用公共领域软件计算它们的位移速率。我发现,在中期和后期A,动粒纤维通过微管通量过程在其两极持续缩短。后期染色体的移动由“吃豆人”机制辅助,即动粒纤维在其染色体界面处缩短。因此,果蝇精母细胞与有丝分裂细胞共享纺锤体动态变化的位点和染色体移动机制。这些数据揭示了光漂白检测方法在测量原代培养物中微管动力学方面的适用性。这种方法可以很容易地应用于其他系统。