Haldenwang W G, Losick R
Proc Natl Acad Sci U S A. 1980 Dec;77(12):7000-4. doi: 10.1073/pnas.77.12.7000.
A modified form of Bacillus subtilis RNA polymerase (RNA nucleotidyltransferase) has been isolated that exhibits distinctive transcriptional specificity. This modified enzyme transcribes two cloned genes from the purA-cysA region of the B. subtilis chromosome whose expression in vivo is associated with the process of sporulation. Neither of these genes is transcribed by the usual form of B. subtilis RNA polymerase holoenzyme containing a sigma factor of 55,000 daltons (sigma 55). The modified RNA polymerase lacks sigma 55 but contains a newly identified subunit of 37,000 daltons termed sigma 37. A reconstitution experiment in which sigma 37 was added to core RNA polymerase strongly suggests that sigma 37 is responsible for the transcriptional specificity of the modified RNA polymerase. Sigma 37 apparently acts at the level of promoter recognition; this transcriptional determinant enabled core RNA polymerase to form stable binary and ternary ("initiation") complexes with endonuclease restriction fragments containing promoters for the cloned B. subtilis genes.
已分离出一种枯草芽孢杆菌RNA聚合酶(RNA核苷酸转移酶)的修饰形式,它表现出独特的转录特异性。这种修饰酶转录来自枯草芽孢杆菌染色体purA - cysA区域的两个克隆基因,其在体内的表达与芽孢形成过程相关。这两个基因都不会被含有55,000道尔顿σ因子(σ55)的枯草芽孢杆菌RNA聚合酶全酶的常见形式转录。修饰后的RNA聚合酶缺乏σ55,但含有一个新鉴定的37,000道尔顿的亚基,称为σ37。将σ37添加到核心RNA聚合酶的重组实验强烈表明,σ37负责修饰后RNA聚合酶的转录特异性。σ37显然在启动子识别水平起作用;这种转录决定因素使核心RNA聚合酶能够与含有枯草芽孢杆菌克隆基因启动子的核酸内切酶限制片段形成稳定的二元和三元(“起始”)复合物。