Buttner M J, Smith A M, Bibb M J
John Innes Institute, Norwich, England.
Cell. 1988 Feb 26;52(4):599-607. doi: 10.1016/0092-8674(88)90472-2.
Using a combination of gel filtration and anion exchange FPLC, three different RNA polymerase holoenzymes from Streptomyces coelicolor A3(2) have been separated. Each holoenzyme transcribes from only one of the four promoters of the S. coelicolor A3(2) dagA gene. Holoenzyme reconstitution experiments identified the sigma factors responsible for recognition of two of the promoters. The previously identified E sigma 49 transcribes from the dagA p3 promoter, whereas a novel species, E sigma 28, recognizes the dagA p2 promoter. Circumstantial evidence suggests that the third holoenzyme, which transcribes from the dagA p4 promoter, is the previously identified E sigma 35. This level of transcriptional complexity supports the idea that RNA polymerase heterogeneity may play a central role in the regulation and coordination of gene expression in this biochemically and morphologically complex bacterium.
利用凝胶过滤和阴离子交换快速蛋白质液相色谱相结合的方法,已分离出天蓝色链霉菌A3(2)的三种不同的RNA聚合酶全酶。每种全酶仅从天蓝色链霉菌A3(2) dagA基因的四个启动子之一进行转录。全酶重组实验确定了负责识别其中两个启动子的σ因子。先前鉴定的Eσ49从dagA p3启动子转录,而一个新的种类Eσ28识别dagA p2启动子。间接证据表明,从dagA p4启动子转录的第三种全酶是先前鉴定的Eσ35。这种转录复杂性水平支持了这样一种观点,即RNA聚合酶的异质性可能在这种生化和形态复杂的细菌的基因表达调控与协调中起核心作用。