Department of Molecular Biosciences, Northwestern University, Evanston, IL 60208-3500, USA.
Phys Biol. 2011 Feb;8(1):015003. doi: 10.1088/1478-3975/8/1/015003. Epub 2011 Feb 7.
Eukaryote cells dramatically reorganize their long chromosomal DNAs to facilitate their physical segregation during mitosis. The internal organization of folded mitotic chromosomes remains a basic mystery of cell biology; its understanding would likely shed light on how chromosomes are separated from one another as well as into chromosome structure between cell divisions. We report biophysical experiments on single mitotic chromosomes from human cells, where we combine micromanipulation, nano-Newton-scale force measurement and biochemical treatments to study chromosome connectivity and topology. Results are in accord with previous experiments on amphibian chromosomes and support the 'chromatin network' model of mitotic chromosome structure. Prospects for studies of chromosome-organizing proteins using siRNA expression knockdowns, as well as for differential studies of chromosomes with and without mutations associated with genetic diseases, are also discussed.
真核细胞在有丝分裂过程中会剧烈重排其长染色体 DNA,以促进染色体的物理分离。折叠的有丝分裂染色体的内部组织仍然是细胞生物学的一个基本奥秘;对其的理解可能有助于阐明染色体彼此分离以及在细胞分裂之间如何分离染色体结构。我们报告了来自人类细胞的单个有丝分裂染色体的生物物理实验,在这些实验中,我们结合了微操作、纳牛顿级力测量和生化处理来研究染色体的连接性和拓扑结构。结果与以前对两栖动物染色体的实验结果一致,并支持有丝分裂染色体结构的“染色质网络”模型。还讨论了使用 siRNA 表达敲低研究染色体组织蛋白的前景,以及对具有和不具有与遗传疾病相关突变的染色体进行差异研究的前景。