Panda C K, Choudhury K, Neogy R K
Chem Biol Interact. 1986 Jan;57(1):65-72. doi: 10.1016/0009-2797(86)90049-9.
Binding of nogalamycin and adriamycin with Sarcoma-180 ascites tumor cell chromatin was studied by a spectrofluorometric method. There was significant reduction in the number of available drug binding sites per nucleotide when the chromatin was digested with DNase I for a period which releases only 7% of the chromosomal DNA. Results indicate preferential binding of these drugs with DNase I hypersensitive sites of chromatin. The DNase-I hypersensitive sites of chromatin were shown to correlate to the sequences required for gene expression. Further digestion with DNase I increases availability of drug binding sites, probably due to relaxation of the compact chromatin.
采用荧光分光光度法研究了诺加霉素和阿霉素与肉瘤180腹水肿瘤细胞染色质的结合。当用DNase I消化染色质一段仅释放7%染色体DNA的时间时,每个核苷酸上可利用的药物结合位点数量显著减少。结果表明这些药物优先与染色质的DNase I超敏位点结合。染色质的DNase-I超敏位点显示与基因表达所需的序列相关。用DNase I进一步消化可增加药物结合位点的可利用性,这可能是由于紧密染色质的松弛所致。