Hancock Ronald
Laval University Cancer Research Centre, Hôtel-Dieu Hospital, 9 rue MacMahon, Quebec, P.Q. G1R 2J6, Canada.
Biol Cell. 2004 Oct;96(8):595-601. doi: 10.1016/j.biolcel.2004.05.003.
Many and possibly all macromolecules in the nucleus are segregated into discrete compartments, but the current model that this is achieved by a fibrillar nuclear matrix which structures the nuclear interior and compartments is not consistent with all experimental observations, as reviewed here. New results are presented which suggest that macromolecular crowding forces play a crucial role in the assembly of at least two compartments, nucleoli and PML bodies, and an in vitro system in which crowding assembles macromolecular complexes into structures which resemble nuclear compartments is described. Crowding forces, which are strong in the nucleus due to the high macromolecule concentration (in the range of 100 mg/ml), vastly increase the association constants of intermolecular interactions and can segregate different macromolecules into discrete phases. The model that they play a role in compartmentalisation of the nucleus is generally consistent with the properties of compartments, including their spherical or quasispherical form and their dynamic and mobile nature.
细胞核中的许多乃至可能所有大分子都被分隔到离散的区室中,但目前认为这是通过构建核内部结构和区室的纤维状核基质来实现的模型,与所有实验观察结果并不一致,如下文所述。本文展示了新的研究结果,这些结果表明大分子拥挤力在至少两个区室(核仁与早幼粒细胞白血病蛋白小体)的组装过程中起着关键作用,并描述了一种体外系统,在该系统中,拥挤效应将大分子复合物组装成类似于核区室的结构。由于高分子浓度较高(在100毫克/毫升范围内),细胞核内的拥挤力很强,极大地增加了分子间相互作用的缔合常数,并能将不同的大分子分隔成离散的相。它们在细胞核区室化过程中发挥作用的模型总体上与区室的特性相符,包括其球形或准球形形态以及动态可移动的性质。