Tumanishvili G D, Jandieri K M, Dzidziguri D V
Differentiation. 1977 Oct 13;8(3):195-9. doi: 10.1111/j.1432-0436.1977.tb00937.x.
It is well known that actinomycin D binds to C-G pairs of DNA. The amount of actinomycin D bound to chromatin thus depends directly on the demasked sites of chromatin DNA. The actinomycin D binding of rat liver chromatin, obtained by the method of Dingman and Sporn, was studied in the presence and absence of liver and kidney nuclear extracts (NE). The actinomycin D binding of liver chromatin increases greatly under the action of liver nuclear extract. No changes occur in liver chromatin actinomycin D binding capacity after the action of kidney NE. The removal of protein or RNA from liver NE removes its ability to change the actinomycin D binding capacity of the liver chromatin. According to the obtained results it may be assumed that the nuclear extract contains the factor which plays a role in controlling cell differentiation.
众所周知,放线菌素D与DNA的C-G碱基对结合。因此,与染色质结合的放线菌素D的量直接取决于染色质DNA的去遮蔽位点。采用丁曼和斯波恩的方法获得大鼠肝脏染色质,研究了在有无肝脏和肾脏核提取物(NE)存在的情况下其与放线菌素D的结合情况。在肝脏核提取物的作用下,肝脏染色质与放线菌素D的结合显著增加。肾脏核提取物作用后,肝脏染色质与放线菌素D的结合能力没有变化。从肝脏核提取物中去除蛋白质或RNA会消除其改变肝脏染色质与放线菌素D结合能力的能力。根据所得结果,可以推测核提取物中含有在控制细胞分化中起作用的因子。