Reudelhuber T L, Ball D J, Davis A H, Garrard W T
Nucleic Acids Res. 1982 Feb 25;10(4):1311-25. doi: 10.1093/nar/10.4.1311.
Electrophoresis fractionates nucleosomes which possess different protein compositions. We report here a procedure for transferring the DNA components of electrophoretically resolved nucleosomes to diazobenzyloxymethyl cellulose (DBM-paper). Histones are first removed from nucleosome components by electrophoresis in the presence of cetyltrimethylammonium bromide (CTAB), leaving DNA fragments fixed within the original gel as the CTAB salts. The DNA is then converted to the sodium salt, denatured, and electrophoretically transferred to DBM-paper. The overall pattern of DNA on the resulting blot is visualized either by fluorography or by immunoautoradiography. This DNA pattern is then compared with autoradiograms obtained after hybridizing the same blot with specific 32P-labeled probes. Using mouse satellite DNA as a hybridization probe, we illustrate the above techniques and demonstrate that nucleosomes carrying satellite sequences are compositionally heterogeneous. The procedures described here should also be useful in the analysis of the nucleic acid components associated with other nucleoprotein complexes.
电泳可分离具有不同蛋白质组成的核小体。我们在此报告一种将电泳分离的核小体的DNA成分转移至重氮苄氧基甲基纤维素(DBM纸)的方法。首先在十六烷基三甲基溴化铵(CTAB)存在下通过电泳从核小体成分中去除组蛋白,使DNA片段作为CTAB盐固定在原始凝胶内。然后将DNA转化为钠盐,变性,并电泳转移至DBM纸。通过荧光自显影或免疫放射自显影观察所得印迹上DNA的整体模式。然后将该DNA模式与用特定的32P标记探针杂交同一印迹后获得的放射自显影片进行比较。使用小鼠卫星DNA作为杂交探针,我们阐述了上述技术,并证明携带卫星序列的核小体在组成上是异质的。这里描述的方法在分析与其他核蛋白复合物相关的核酸成分时也应是有用的。