Widmer R M, Lucchini R, Lezzi M, Meyer B, Sogo J M, Edström J E, Koller T
EMBO J. 1984 Jul;3(7):1635-41. doi: 10.1002/j.1460-2075.1984.tb02022.x.
We examined the chromatin structure of a Balbiani ring (secretory protein gene) in the salivary glands of Chironomus larvae in its hyperactive state after stimulation with pilocarpine. For the inactive state of the gene an established tissue culture cell line, not expressing the gene, was used. Electron microscopy showed an RNA polymerase density of approximately 38/microns. Micrococcal nuclease digestion of purified nuclei followed by DNA transfer and hybridization revealed a smear with no recognizable discrete DNA fragments. Without pilocarpine stimulation a faint nucleosomal repeat was superimposed upon the smear, and in tissue culture cells a clear nucleosomal repeat was revealed. The restriction enzyme XbaI, which has a 6-bp recognition sequence, cut the gene in the hyperactive chromatin state, but not in its inactive conformation. The combined results are best explained by the absence of most of the nucleosomes in this hyperactive RNA polymerase II transcribed gene.
我们研究了经毛果芸香碱刺激后处于高活性状态的摇蚊幼虫唾液腺中一个巴尔比亚尼环(分泌蛋白基因)的染色质结构。对于该基因的非活性状态,使用了一个不表达该基因的已建立的组织培养细胞系。电子显微镜显示RNA聚合酶密度约为38/微米。对纯化的细胞核进行微球菌核酸酶消化,然后进行DNA转移和杂交,结果显示为一片模糊,没有可识别的离散DNA片段。在没有毛果芸香碱刺激的情况下,一片模糊之上叠加有微弱的核小体重复信号,而在组织培养细胞中则显示出清晰的核小体重复信号。具有6碱基对识别序列的限制性内切酶XbaI在该基因处于高活性染色质状态时能切割它,但在其非活性构象时则不能。这些综合结果最好的解释是,在这个由RNA聚合酶II转录的高活性基因中,大多数核小体不存在。