Department of Physics, Nabadwip Vidyasagar College, Nabadwip, Nadia 741302, India, TIFR Centre for Interdisciplinary Sciences, 21 Brundavan Colony, Narsingi, Hyderabad 500075, India, Centre for Advanced Materials, Indian Association for the Cultivation of Science, Jadavpur, Kolkata 700032, India, The Institute of Mathematical Sciences, C.I.T. Campus, Taramani, Chennai 600 113, India, Mechanobiology Institute, National University of Singapore, T-Lab, #10-01, 5A Engineering Drive 1, Singapore 117411, Singapore and Department of Biological Sciences, National University of Singapore, 14 Science Drive 4, Singapore 117543, Singapore.
Nucleic Acids Res. 2014 Apr;42(7):4145-59. doi: 10.1093/nar/gkt1417. Epub 2014 Jan 22.
Chromosomes within eukaryotic cell nuclei at interphase are not positioned at random, since gene-rich chromosomes are predominantly found towards the interior of the cell nucleus across a number of cell types. The physical mechanisms that could drive and maintain the spatial segregation of chromosomes based on gene density are unknown. Here, we identify a mechanism for such segregation, showing that the territorial organization of chromosomes, another central feature of nuclear organization, emerges naturally from our model. Our computer simulations indicate that gene density-dependent radial segregation of chromosomes arises as a robust consequence of differences in non-equilibrium activity across chromosomes. Arguing that such differences originate in the inhomogeneous distribution of ATP-dependent chromatin remodeling and transcription machinery on each chromosome, we show that a variety of non-random positional distributions emerge through the interplay of such activity, nuclear shape and specific interactions of chromosomes with the nuclear envelope. Results from our model are in reasonable agreement with experimental data and we make a number of predictions that can be tested in experiments.
有丝分裂间期真核细胞核内的染色体并非随机定位,因为富含基因的染色体主要存在于细胞核内部,这在多种细胞类型中都有体现。但基于基因密度驱动和维持染色体空间分离的物理机制尚不清楚。在这里,我们确定了一种这样的分离机制,表明染色体的区域化组织(核组织的另一个核心特征)自然地从我们的模型中出现。我们的计算机模拟表明,染色体的基因密度依赖性的径向分离是由于染色体之间的非平衡活性差异而产生的稳健结果。我们认为这种差异起源于每个染色体上的 ATP 依赖性染色质重塑和转录机制的不均匀分布,并表明通过这种活性、核形状以及染色体与核膜的特定相互作用的相互作用,会出现各种非随机的位置分布。我们模型的结果与实验数据基本一致,并且我们提出了一些可以通过实验来验证的预测。