Akiyoshi H, Fujii S
J Biochem. 1978 Aug;84(2):337-42. doi: 10.1093/oxfordjournals.jbchem.a132133.
Nucleosomes isolated from Yoshida sarcoma chromatin by micrococcal nuclease treatment were relatively inactive as templates for in vitro DNA synthesis. However, the template activity increased by trypsin digestion of nucleosomes or addition of heparin to the reaction mixture. This indicates that the nucleosomal template activity is masked. A crude extract of Yoshida sarcoma cells stimulated the nucleosomal template activity. The stimulatory factor was separated into three peaks by DEAE cellulose column chromatography. The same three peaks were observed in normal rat liver extract with much lower activities, but enhanced in regenerating liver. The factors seem to stimulate DNA synthesis by activating DNA template in nucleosomes without degrading histones or changing the primary structure of nucleosomal DNA.
经微球菌核酸酶处理从吉田肉瘤染色质中分离出的核小体作为体外DNA合成的模板相对无活性。然而,通过对核小体进行胰蛋白酶消化或向反应混合物中添加肝素,模板活性会增加。这表明核小体模板活性被掩盖了。吉田肉瘤细胞的粗提取物刺激了核小体模板活性。通过DEAE纤维素柱色谱法将刺激因子分离为三个峰。在正常大鼠肝脏提取物中观察到相同的三个峰,但其活性低得多,而在再生肝脏中活性增强。这些因子似乎通过激活核小体中的DNA模板来刺激DNA合成,而不会降解组蛋白或改变核小体DNA的一级结构。