Cataldi A, Lisio R, Rana R, Bareggi R, Tulipano G, Miscia S
Istituto di Morfologia Umana Normale, Università di Chieti, Italy.
Exp Cell Res. 1993 Jan;204(1):167-9. doi: 10.1006/excr.1993.1021.
The DNase I sensitivity of total chromatin has been analyzed in nuclei isolated from control and interferon-treated Daudi cells. The electrophoretic analysis of DNA has evidenced a different pattern of DNA fragment size produced by DNase I in nuclei isolated from control cells compared to interferon-treated samples. This feature is supported by a different recovery of acid soluble chromatin and is accompanied by modifications of in vitro RNA synthesis along with initiation and elongation of RNA chains. No changes have been evidenced in nuclei isolated from Daudi-resistant cells under the same experimental conditions. These data might be interpreted as a transient modulation, induced by interferon, of chromatin structure in terms of chromatin condensation which, in turn, activates the RNA synthesis after the transduction into the nucleus of the interferon-generated signals.
已对从对照和干扰素处理的Daudi细胞中分离出的细胞核中的总染色质的脱氧核糖核酸酶I敏感性进行了分析。DNA的电泳分析表明,与干扰素处理的样品相比,从对照细胞中分离出的细胞核中,脱氧核糖核酸酶I产生的DNA片段大小模式不同。这一特征得到了酸溶性染色质不同回收率的支持,并伴随着体外RNA合成的改变以及RNA链起始和延伸的变化。在相同实验条件下,从抗Daudi细胞中分离出的细胞核未发现变化。这些数据可以解释为,干扰素诱导染色质结构发生瞬时调节,表现为染色质凝聚,进而在干扰素产生的信号转导至细胞核后激活RNA合成。