Huang C H, Baserga R
Nucleic Acids Res. 1976 Aug;3(8):1857-73. doi: 10.1093/nar/3.8.1857.
Circular dichroism in the 300-360 nm region and fluorescence induced by intercaltating binding of ethidum bromide to both DNA and RNA components were studied in isolated HeLa nucleoli. Both DNA and RNA compoents contribute to the induced dichroic elliticity. Digestion of nucleoli by RNase or DNase shows that most of the induced ellipticity comes from the DNA component. In nucleoli with an RNA/DNA = 0.8/1.0 the RNA component gives only 20% of the total ellipticity when measured at an ethidium bromide/DNA = 0.25. Spectro-fluorometric titration shows that ethidium bromide intercalates mostly into DNA in nucleoli. Both circular dichroism and fluorescence studies indicate that both DNA and RNA components in isolated nucleoli are less accessible to intercalating binding by ethidium bromide when compared to purified nucleolar DNA, DNA in chromatin or purified ribosomal RNA. Circular dichroic measurements of intercalating binding of ethidium bromide to to nucleoli may be used to study changes in nucleoli under different physiological or pathological conditions.
在分离的HeLa核仁中研究了300 - 360nm区域的圆二色性以及溴化乙锭与DNA和RNA成分插入结合所诱导的荧光。DNA和RNA成分都对诱导的二色性椭圆率有贡献。用核糖核酸酶或脱氧核糖核酸酶消化核仁表明,大部分诱导椭圆率来自DNA成分。在RNA/DNA = 0.8/1.0的核仁中,当溴化乙锭/DNA = 0.25时测量,RNA成分仅占总椭圆率的20%。光谱荧光滴定表明,溴化乙锭主要插入核仁中的DNA。圆二色性和荧光研究均表明,与纯化的核仁DNA、染色质中的DNA或纯化的核糖体RNA相比,分离核仁中的DNA和RNA成分对溴化乙锭插入结合的可及性较低。溴化乙锭与核仁插入结合的圆二色性测量可用于研究不同生理或病理条件下核仁的变化。