Sir William Dunn School of Pathology, University of Oxford, South Parks Road, Oxford, OX1 3RE, UK.
Chromosome Res. 2011 Jan;19(1):53-61. doi: 10.1007/s10577-010-9150-y.
Four specific forces (H-bonds, van der Waals forces, hydrophobic and charge interactions) shape the structure of proteins, and many biologists assume they will determine the shape of all structures in the cell. However, as the mass and contour length of a human chromosome are ~7 orders of magnitude larger than those of a typical protein, additional forces can become significant. We review evidence that additional non-specific (entropic) forces are major determinants of chromosomal shape and position. They are sufficient to drive the segregation (de-mixing) of newly replicated DNA to the poles of bacterial cells, while an entropic centrifuge can both form human chromosomes into territories and position them appropriately in nuclei; more locally, a depletion attraction can loop bacterial and human genomes.
四种特定的力(氢键、范德华力、疏水力和电荷相互作用)塑造了蛋白质的结构,许多生物学家假设它们将决定细胞中所有结构的形状。然而,由于人类染色体的质量和轮廓长度比典型蛋白质大约 7 个数量级,因此其他力也可能变得重要。我们回顾了证据,表明额外的非特异性(熵)力是染色体形状和位置的主要决定因素。它们足以驱动新复制的 DNA 分离(去混合)到细菌细胞的两极,而熵离心力既能将人类染色体形成区域,又能将它们在核内适当地定位;更局部地说,耗竭吸引可以使细菌和人类基因组形成环。