Aldea M, Claverie-Martín F, Díaz-Torres M R, Kushner S R
Department of Genetics, University of Georgia, Athens 30602.
Gene. 1988 May 15;65(1):101-10. doi: 10.1016/0378-1119(88)90421-0.
A simple method for RNA transcript mapping has been developed that combines the use of 35S-labeled M13 DNA probes and the presence of high concentrations of sodium trichloroacetate in the hybridization buffer. These hybridization conditions permit the use of M13 probes without purification from the template. The dideoxy sequencing ladders used for sizing the protected DNA fragments are obtained from the same M13 templates utilized to synthesize the DNA probes. The method was tested by analyzing the transcripts controlled by lac, ptr and trxA promoters. Comparison of the results with previously published data obtained with the conventional S1 nuclease mapping technique indicated that the present method is just as precise and at least 50 times more sensitive. Clones constructed for sequencing a gene of interest can be used directly to identify transcriptional start points.
已开发出一种简单的RNA转录本定位方法,该方法结合了使用35S标记的M13 DNA探针以及在杂交缓冲液中存在高浓度的三氯乙酸钠。这些杂交条件允许使用未经模板纯化的M13探针。用于确定受保护DNA片段大小的双脱氧测序梯状图谱是从用于合成DNA探针的相同M13模板获得的。通过分析由lac、ptr和trxA启动子控制的转录本对该方法进行了测试。将结果与先前使用传统S1核酸酶定位技术获得的数据进行比较表明,本方法同样精确且灵敏度至少高50倍。为对感兴趣的基因进行测序而构建的克隆可直接用于鉴定转录起始点。