Brack C
Proc Natl Acad Sci U S A. 1979 Jul;76(7):3164-8. doi: 10.1073/pnas.76.7.3164.
An electron microscope technique is described that allows rapid characterization of transcription in vitro. DNA is transcribed with Escherichia coli RNA polymerase in vitro, and the RNA is hybridized to its template. Measurement of the resulting transcription R-loop molecules allows accurate mapping of transcription initiation sites (promoter sites) and analysis of the direction and rate of transcription and the level of transcription from each initiation site. The two major early promoters pR and pL of bacteriophage lambda have been mapped within 0.1-0.3 map units of the known positions and three additional sites have been confirmed. Six transcription initiation sites have been preliminarily mapped on plasmid pSF2124 DNA.
本文描述了一种电子显微镜技术,该技术可快速对体外转录进行表征。在体外,用大肠杆菌RNA聚合酶转录DNA,然后将RNA与其模板杂交。对由此产生的转录R环分子进行测量,可精确绘制转录起始位点(启动子位点),并分析转录的方向、速率以及每个起始位点的转录水平。噬菌体λ的两个主要早期启动子pR和pL已被定位在已知位置的0.1 - 0.3个图谱单位内,另外三个位点也已得到确认。在质粒pSF2124 DNA上已初步绘制出六个转录起始位点。