Pipkin J L, Anson J F, Hinson W G, Burns E R
Cell Biol Int Rep. 1984 Apr;8(4):279-87. doi: 10.1016/0309-1651(84)90154-1.
The H1 subtype proteins a, b, c, d, e, and 1 degree and the high mobility group (HMG) proteins 14 and 17 were extracted from submaxillary gland (SMG) nuclei treated in vivo and sorted from specific phases of the cell cycle, and analyzed by gel electrophoresis. Significant differences in these proteins were noted between quiescent (GO) phase nuclei and proliferating nuclei in both stained and autoradiographic gels. Stimulation of the SMG into cell division with DL-isoproterenol-HCl alone or in conjunction with sodium phenobarbital (PB) provided a system for the analysis of drug effects in stained, 3H lysine, and 32P pulse-labeled nuclear proteins obtained from different phases of the cell cycle.
从经体内处理的颌下腺(SMG)细胞核中提取H1亚型蛋白质a、b、c、d、e、1°以及高迁移率族(HMG)蛋白质14和17,并从细胞周期的特定阶段进行分选,然后通过凝胶电泳进行分析。在染色凝胶和放射自显影凝胶中,静止(G0)期细胞核与增殖细胞核之间的这些蛋白质存在显著差异。单独用DL - 异丙肾上腺素 - HCl或与苯巴比妥钠(PB)联合刺激SMG进行细胞分裂,提供了一个系统,用于分析从细胞周期不同阶段获得的染色、3H赖氨酸和32P脉冲标记核蛋白中的药物作用。