Clark D J, Thomas J O
J Mol Biol. 1986 Feb 20;187(4):569-80. doi: 10.1016/0022-2836(86)90335-9.
The nature of the complexes formed between histone H1 and linear double-stranded DNA is dependent on ionic strength and on the H1 : DNA ratio. At an input ratio of less than about 60% (w/w) H1 : DNA, there is a sharp transition from non-co-operative to co-operative binding at a critical salt concentration that depends on the DNA size and is in the range 20 to 50 mM-NaCl. Above this critical ionic strength the H1 binds to only some of the DNA molecules leaving the rest free, as shown by sedimentation analysis. The ionic strength range over which this change in behaviour occurs is also that over which chromatin folding is induced. Above the salt concentration required for co-operative binding of H1 to DNA, but not below it, H1 molecules are in close proximity as shown by the formation of H1 polymers upon chemical cross-linking. The change in binding mode is not driven by the folding of the globular domain of H1, since this is already folded at low salt in the presence of DNA, as indicated by its resistance to tryptic digestion. The H1-DNA complexes at low salt, where H1 is bound distributively to all DNA molecules, contain thickened regions about 6 nm across interspersed with free DNA, as shown by electron microscopy. The complexes formed at higher salt through co-operative interactions are rods of relatively uniform width (11 to 15 nm) whose length is about 1.6 times shorter than that of the input DNA, or are circular if the DNA is long enough. They contain approximately 70% (w/w) H1 : DNA and several DNA molecules. These thick complexes can also be formed at low salt (15 mM-NaCl) when the H1 : DNA input ratio is sufficiently high (approximately 70%).
组蛋白H1与线性双链DNA形成的复合物的性质取决于离子强度和H1与DNA的比例。当H1与DNA的输入比例小于约60%(w/w)时,在取决于DNA大小且在20至50 mM-NaCl范围内的临界盐浓度下,会从非协同结合急剧转变为协同结合。高于此临界离子强度时,如沉降分析所示,H1仅与一些DNA分子结合,其余的则保持游离状态。这种行为变化发生的离子强度范围也是诱导染色质折叠的范围。高于H1与DNA协同结合所需的盐浓度(但不是低于此浓度)时,如化学交联后形成H1聚合物所示,H1分子彼此靠近。结合模式的变化不是由H1球状结构域的折叠驱动的,因为在DNA存在下低盐时它已经折叠,这由其对胰蛋白酶消化的抗性表明。低盐时H1与DNA的复合物中,H1分散地结合到所有DNA分子上,电子显微镜显示其中散布着约6纳米宽的增厚区域和游离DNA。在较高盐浓度下通过协同相互作用形成的复合物是宽度相对均匀(11至15纳米)的棒状结构,其长度比输入DNA的长度短约1.6倍,如果DNA足够长则为环状。它们含有约70%(w/w)的H1与DNA以及几个DNA分子。当H1与DNA的输入比例足够高(约70%)时,在低盐(15 mM-NaCl)条件下也能形成这些致密复合物。