Protas A F, Khrapunov S N, Berdyshev G D
Ukr Biokhim Zh (1978). 1984 Nov-Dec;56(6):603-8.
The process of dimer (H2A-H2B), tetramer (H3-H4)2 and octamer (H3-H4-H2A-H2B)2 formation was analyzed by the methods of gel-filtration and differential spectrophotometry. Histone octamer with the parameters most close to the native ones is established to be reconstructed only from denaturated monomers at neutral pH. The necessary condition for formation of histone octamer is the stage of tetramer (H3-H4)2 and (H2A-H2B) formation. Histone H3 with intramolecular disulphide bond (formula: see text) does not form tetramer (H3-H4)2 and is not a part of octamer. When passing through the dimer (H3-H4) stage it produces nonspecific high-molecular aggregates. Structural changes preceding the formation of histone octamer may play a significant role for transition of chromatin and nucleosomes into the transcription-active, repressed and other states.
通过凝胶过滤和差示分光光度法分析了二聚体(H2A-H2B)、四聚体(H3-H4)2和八聚体(H3-H4-H2A-H2B)2的形成过程。已确定只有在中性pH条件下从变性单体重建的组蛋白八聚体的参数最接近天然参数。形成组蛋白八聚体的必要条件是四聚体(H3-H4)2和(H2A-H2B)的形成阶段。具有分子内二硫键的组蛋白H3(分子式:见正文)不形成四聚体(H3-H4)2,也不是八聚体的一部分。当经过二聚体(H3-H4)阶段时,它会产生非特异性高分子聚集体。组蛋白八聚体形成之前的结构变化可能对染色质和核小体转变为转录活性、抑制和其他状态起重要作用。