Hay C W, Candido E P
J Biol Chem. 1983 Mar 25;258(6):3726-34.
The chromatin-bound histone deacetylase of HeLa cells has been studied using endogenous [3H]acetyl-labeled polynucleosomes containing the enzyme, prepared in the presence of 40 mM butyrate. Histone deacetylase was assayed upon removal of the butyrate, and it was found that active enzyme is found only in association with a high molecular weight complex. This deacetylase-containing complex is relatively resistant to digestion with micrococcal nuclease. No activity is found on mononucleosomes or oligonucleosomes. Up to 90% of labeled acetyl groups are removed from histone deacetylase complexes incubated in the absence of butyrate. Free histones are a poor substrate under these conditions, but histones in mononucleosomes are deacetylated when they are incubated with histone deacetylase complex. Histone deacetylase remains bound to this complex in 1-2 M NaCl and does not dissociate from it during its reaction with acetylated core histones. Under typical nuclease digestion conditions, the histone deacetylase complex contains DNA with a size distribution of 5-11 kilobase pairs and a variety of nonhistone proteins. Comparison of the protein composition of histone deacetylase complexes with that of nuclear matrix preparations shows some similarities. Taken together, the results on the chromatographic behavior, the DNA fragment sizes, and the protein composition of the deacetylase complex suggest that protein-protein interactions may be important in maintaining its structure and also in the binding of the deacetylase itself to the complex.
利用在40 mM丁酸盐存在下制备的含有该酶的内源性[3H]乙酰标记多聚核小体,对HeLa细胞中与染色质结合的组蛋白脱乙酰酶进行了研究。在去除丁酸盐后对组蛋白脱乙酰酶进行了测定,发现活性酶仅与一种高分子量复合物相关联。这种含脱乙酰酶的复合物对微球菌核酸酶的消化相对抗性较强。在单核小体或寡核小体上未发现活性。在不存在丁酸盐的情况下孵育的组蛋白脱乙酰酶复合物中,高达90%的标记乙酰基被去除。在这些条件下,游离组蛋白是一种较差的底物,但单核小体中的组蛋白与组蛋白脱乙酰酶复合物一起孵育时会发生去乙酰化。组蛋白脱乙酰酶在1-2 M NaCl中仍与该复合物结合,并且在其与乙酰化核心组蛋白反应期间不会从复合物中解离。在典型的核酸酶消化条件下,组蛋白脱乙酰酶复合物含有大小分布为5-11千碱基对的DNA和多种非组蛋白。将组蛋白脱乙酰酶复合物的蛋白质组成与核基质制剂的蛋白质组成进行比较,发现了一些相似之处。综合来看,关于脱乙酰酶复合物的色谱行为、DNA片段大小和蛋白质组成的结果表明,蛋白质-蛋白质相互作用可能在维持其结构以及脱乙酰酶本身与复合物的结合中起重要作用。