Bode J, Henco K, Wingender E
Eur J Biochem. 1980 Sep;110(1):143-52. doi: 10.1111/j.1432-1033.1980.tb04849.x.
A rapid procedure for the isolation of core particles from Chinese hamster ovary cells is described which permits measurements, usually at the day of their preparation. Particles of 145 +/- 5 base pairs, derived from interphase cells, will be compared with the analogue specimens from butyrate-treated cells, metaphase cells and a standard preparation from chicken erythrocytes. Butyrate cause an increase in the acetylation of histones H3 and H4, which induces alterations of the interhistone and histone-DNA interactions. Changes in the interhistone contacts, correlated to an extension of alpha-helical segments, lead to an altered accessibility of the H3 cysteine side-chains and to a different histone displacement by protamines. On the other hand, histone-DNA contacts are loosened in parts and this is particularly evident from the changes in the premelting region of a thermal-denaturation profile.
本文描述了一种从中国仓鼠卵巢细胞中快速分离核心颗粒的方法,该方法通常允许在制备当天进行测量。将来自间期细胞的145±5个碱基对的颗粒与来自丁酸盐处理细胞、中期细胞的类似标本以及鸡红细胞的标准制剂进行比较。丁酸盐会导致组蛋白H3和H4乙酰化增加,从而诱导组蛋白间和组蛋白-DNA相互作用的改变。组蛋白间接触的变化与α-螺旋段的延长相关,导致H3半胱氨酸侧链的可及性改变以及鱼精蛋白对组蛋白的不同置换。另一方面,组蛋白-DNA接触部分松弛,这从热变性图谱的预熔区变化中尤为明显。