Simola K, Selander R K, de la Chapelle A, Corneo G, Ginelli E
Chromosoma. 1975 Jul 21;51(3):199-205. doi: 10.1007/BF00284814.
The effects of mouse satellite, main band and total DNA on the fluorescence intensity of quinacrine and of the bibenzimidazole derivative Hoechst 33258 were tested in solution. No significant differences were noticed between the double-stranded DNAs in spite of the 5% difference in AT-content between satellite and main band DNA. Single-stranded DNAs enhanced the fluorescence intensity of Hoechst 33258 far less than double-stranded DNAs. Having been denaturated and then reassociated the DNA fractions were intermediate in their enhancing effects on the fluorescence intensity of Hoechst 33258, the differences presumably being due to different degrees of reassociation. The effect of denatured and subsequently reassociated satellite DNA on the fluorescence intensity of quinacrine was similar to that of the native DNAs. Main band and total DNA quenched the fluorescence intensity of quinacrine more after denaturation-reassociation than it did when native. In the discussion the results are related to known cytological data.
在溶液中测试了小鼠卫星DNA、主带DNA和总DNA对喹吖因及双苯并咪唑衍生物Hoechst 33258荧光强度的影响。尽管卫星DNA和主带DNA的AT含量有5%的差异,但双链DNA之间未观察到显著差异。单链DNA增强Hoechst 33258荧光强度的程度远低于双链DNA。DNA片段变性后再复性,其对Hoechst 33258荧光强度的增强作用处于中间水平,差异可能是由于复性程度不同所致。变性后再复性的卫星DNA对喹吖因荧光强度的影响与天然DNA相似。主带DNA和总DNA变性 - 复性后对喹吖因荧光强度的淬灭作用比天然时更强。在讨论中,将这些结果与已知的细胞学数据相关联。