Walker P R, Sikorska M
J Biol Chem. 1987 Sep 5;262(25):12223-7.
Sedimentation analysis has been used to compare the structure of 30-nm chromatin fibers, isolated and digested under conditions that maintain the native structure, with relaxed-refolded chromatin. The native chromatin fibers show sharp, ionic strength-dependent changes in sedimentation coefficient that are not apparent in relaxed-refolded fibers. The first transition at approximately 20 mM ionic strength reflects the organization of the 10-nm polynucleosome chain into a loose helically coiled 30-nm fiber. Between 20 and 60 mM ionic strength there is considerable interaction between nucleosomes within the coils to generate a stable helical array with 12 nucleosomes/turn. Above 60 mM ionic strength the helical coil continues to condense until it precipitates at ionic strengths slightly greater than those considered physiological, indicating that there is no end point in fiber formation. The data is incompatible with a solenoid model with 6 nucleosomes/turn and also rules out the existence of a beaded subunit structure.
沉降分析已被用于比较在维持天然结构的条件下分离并消化的30纳米染色质纤维与松弛再折叠染色质的结构。天然染色质纤维在沉降系数上表现出尖锐的、依赖离子强度的变化,而这些变化在松弛再折叠的纤维中并不明显。在大约20 mM离子强度下的第一次转变反映了10纳米多核小体链组织成松散的螺旋盘绕30纳米纤维。在20至60 mM离子强度之间,线圈内的核小体之间存在相当大的相互作用,以产生每圈12个核小体的稳定螺旋阵列。高于60 mM离子强度时,螺旋线圈继续浓缩,直到在略高于生理离子强度的条件下沉淀,这表明纤维形成没有终点。该数据与每圈6个核小体的螺线管模型不相符,也排除了串珠状亚基结构的存在。