Varshavskiĭ A I, Bakaev V V, Il'in I V, Baev A A, Kadykov V A
Mol Biol (Mosk). 1976 Jan-Feb;10(1):35-54.
Chromatin which was hydrodynamically sheared in a low ionic strength buffer lacking divalent cations (mu = 0.005) contains a heterogeneous set of DNP particles but no molecules of free DNA. The main finding is that a transference of sheared chromatin to 1-2 mM MgCl2 or to 0.1-0.2M NaCl results in the appearance of completely free DNA molecules. A salt-induced rearrangementof DNA-bound histones, but not a partial loss of them is responsible for the observed phenomenon. Formation of free DNA molecules is accompanied by aggregation of the majority of remaining DNP particles. Percentage of free DNA molecules in the chromatin which was sheared to an average DNA length of approx. 400 base pairs is increased from zero in the initial DNP sample to 8-9% in 1 mM MgCl2 and further to 30-31% of the total DNA in 0.30 M NaCl, 2 mM MgCl2. Free DNA molecules in the sheared chromatin are observed not only upon isopycnic banding of formaldehyde-fixed DNP in CsCl gradients but also in non-ionic Metrizamide gradients with either fixed or unfixed DNP samples. Process of free DNA formation is a reversible one; its direction and the equilibrium state depend in particular on the ionic conditions of the medium. Percentage of free DNA molecules in the sheared chromatin at a given ionic strength of solution is strongly decreased upon an increase of the average length of DNA in the DNP particles. Several lines of evidence suggest that free DNA molecules are formed in the sheared chromatin as a result of cooperative rearrangements of histones in salt-induced DNP aggregates. A dynamical model of chromosomal fiber is proposed on the basis of the present and earlier experimental data [1]. According to the model histones are arranged on DNA in clusters separated by stretches of free DNA. A salt-induced migration of histones along or between DNP fibers can result in unification of different clusters, thereby generating longer stretches of free DNA, the total amount of free DNA being approximately constant. Possible in vivo significance of such a dynamical structure is discussed.
在缺乏二价阳离子(μ = 0.005)的低离子强度缓冲液中通过流体动力学剪切的染色质含有一组异质的脱氧核糖核蛋白(DNP)颗粒,但没有游离DNA分子。主要发现是,将剪切后的染色质转移到1 - 2 mM MgCl₂ 或0.1 - 0.2 M NaCl中会导致完全游离的DNA分子出现。盐诱导的与DNA结合的组蛋白重排,而非组蛋白的部分丢失,是导致观察到的现象的原因。游离DNA分子的形成伴随着大多数剩余DNP颗粒的聚集。在剪切至平均DNA长度约为400个碱基对的染色质中,游离DNA分子的百分比从初始DNP样品中的零增加到1 mM MgCl₂ 中的8 - 9%,并进一步增加到0.30 M NaCl、2 mM MgCl₂ 中总DNA的30 - 31%。在剪切后的染色质中,游离DNA分子不仅在CsCl梯度中甲醛固定的DNP的等密度梯度离心时被观察到,而且在固定或未固定的DNP样品的非离子型甲泛葡胺梯度中也被观察到。游离DNA形成过程是可逆的;其方向和平衡状态尤其取决于介质的离子条件。在给定溶液离子强度下,剪切后的染色质中游离DNA分子的百分比会随着DNP颗粒中DNA平均长度的增加而大幅降低。几条证据表明,游离DNA分子是在剪切后的染色质中由于盐诱导的DNP聚集体中组蛋白的协同重排而形成的。基于目前和早期的实验数据[1]提出了染色体纤维的动力学模型。根据该模型,组蛋白以由游离DNA片段隔开的簇的形式排列在DNA上。盐诱导的组蛋白沿着DNP纤维或在DNP纤维之间迁移可导致不同簇的合并,从而产生更长的游离DNA片段,游离DNA的总量大致恒定。讨论了这种动态结构可能的体内意义。