Scaife J G, Heilig J S, Rowen L, Calendar R
Proc Natl Acad Sci U S A. 1979 Dec;76(12):6510-4. doi: 10.1073/pnas.76.12.6510.
The genes for the RNA polymerase sigma subunit (rpoD) and DNA primase (dnaG) of Salmonella typhimurium have been cloned into lambda vectors. Combined restriction, deletion and functional analysis of the cloned fragment allows us to map the genes precisely on the fragment, establishes the direction in which rpoD is transcribed, and reveals the existence of at least one new gene in the vicinity. A closely homologous, smaller fragment of Escherichia coli DNA, also cloned into lambda, contains rpoD and at least part of dnaG.
鼠伤寒沙门氏菌RNA聚合酶σ亚基(rpoD)和DNA引发酶(dnaG)的基因已被克隆到λ载体中。对克隆片段进行限制性内切酶联合分析、缺失分析和功能分析,使我们能够在该片段上精确绘制这些基因图谱,确定rpoD的转录方向,并揭示其附近至少存在一个新基因。同样克隆到λ载体中的一段与大肠杆菌DNA密切同源的较小片段,包含rpoD和至少部分dnaG。