Yager T D, McMurray C T, van Holde K E
Department of Biochemistry and Biophysics, Oregon State University, Corvallis 97331-6503.
Biochemistry. 1989 Mar 7;28(5):2271-81. doi: 10.1021/bi00431a045.
At elevated salt concentrations, the structure of chromatin is destabilized. This paper is concerned with the processes by which DNA is released from nucleosome core particles in free, uncomplexed form. Our experiments indicate that the DNA release reaction has distinctly different characteristics below and above approximately 0.75 M NaCl. Below this concentration of salt, release of the histones from the DNA is highly cooperative, so that no dissociation intermediates are even seen. Above this salt concentration, histone release is not so cooperative; H2A and H2B are released from the DNA more readily than are H3 and H4. This results in an apparently heterogeneous population of (H2A, H2B)-depleted intermediate species sedimenting at rates between that of free DNA and that of intact core particles. Dissociation of core particles at NaCl concentrations below 0.75 M is readily reversible. Reassociation of DNA and histones from higher salt concentrations is nearly quantitative if carried out by gradual decrease of salt concentration, but rapid dilution to low salt results in the formation of a fraction of metastable nucleosome multimers. To help organize our description of the DNA release process, we introduce a stability diagram for the core particle, defined with respect to the independent variables of salt concentration and particle concentration. We draw upon our own experimental work and also upon the work of several other laboratories. We distinguish five major regions in this diagram.
在盐浓度升高时,染色质的结构会变得不稳定。本文关注的是DNA以游离、未复合的形式从核小体核心颗粒中释放出来的过程。我们的实验表明,在约0.75 M NaCl浓度上下,DNA释放反应具有明显不同的特征。在该盐浓度以下,组蛋白从DNA上的释放具有高度协同性,以至于甚至看不到解离中间体。在该盐浓度以上,组蛋白释放的协同性没那么高;H2A和H2B比H3和H4更容易从DNA上释放出来。这导致出现了明显异质的、缺少(H2A,H2B)的中间物种群体,其沉降速率介于游离DNA和完整核心颗粒之间。在NaCl浓度低于0.75 M时核心颗粒的解离很容易逆转。如果通过逐渐降低盐浓度来进行,从较高盐浓度下使DNA和组蛋白重新结合几乎是定量的,但快速稀释至低盐会导致形成一部分亚稳态核小体多聚体。为了便于组织我们对DNA释放过程的描述,我们引入了一个核心颗粒的稳定性图,该图是根据盐浓度和颗粒浓度这两个自变量来定义的。我们借鉴了我们自己的实验工作以及其他几个实验室的工作。我们在该图中区分出五个主要区域。