Neurohr Gabriel, Gerlich Daniel W
Institute of Biochemistry, Swiss Institute of Technology Zurich (ETHZ), Schafmattstr. 18, CH-8093 Zurich, Switzerland.
Chromosome Res. 2009;17(2):145-54. doi: 10.1007/s10577-008-9010-1.
The dynamic reorganization of chromatin into rigid and compact mitotic chromosomes is of fundamental importance for faithful chromosome segregation. Owing to the difficulty of investigating this process under physiological conditions, the exact morphological transitions and the molecular machinery driving chromosome condensation remain poorly defined. Here, we review how imaging-based methods can be used to quantitate chromosome condensation in vivo, focusing on yeast and animal tissue culture cells as widely used model systems. We discuss approaches how to address structural dynamics of condensing chromosomes and chromosome segments, as well as to probe for mechanical properties of mitotic chromosomes. Application of such methods to systematic perturbation studies will provide a means to reveal the molecular networks underlying the regulation of mitotic chromosome condensation.
染色质动态重组成刚性且紧密的有丝分裂染色体对于准确的染色体分离至关重要。由于在生理条件下研究这一过程存在困难,驱动染色体凝聚的确切形态转变和分子机制仍不清楚。在这里,我们综述了基于成像的方法如何用于在体内定量染色体凝聚,重点关注酵母和动物组织培养细胞这两种广泛使用的模型系统。我们讨论了如何研究凝聚染色体和染色体片段的结构动态,以及探测有丝分裂染色体的力学性质的方法。将这些方法应用于系统性扰动研究将为揭示有丝分裂染色体凝聚调控背后的分子网络提供一种手段。