Milano A, Forti F, Sala C, Riccardi G, Ghisotti D
Dipartimento di Genetica e Microbiologia A. Buzzati Traverso, Università di Pavia, Pavia, Italy.
J Bacteriol. 2001 Dec;183(23):6801-6. doi: 10.1128/JB.183.23.6801-6806.2001.
The DNA region upstream of katG in Mycobacterium smegmatis was cloned and sequenced. The furA gene, highly homologous to Mycobacterium tuberculosis furA, mapped in this region. The furA-katG organization appears to be conserved among several mycobacteria. The transcription pattern of furA and katG in M. smegmatis upon oxidative stress was analyzed by Northern blotting and primer extension. Although transcription of both furA and katG was induced upon oxidative stress, transcripts covering both genes could not be identified either by Northern blotting or by reverse transcriptase PCR. Specific transcripts and 5' ends were identified for furA and katG, respectively. By cloning M. smegmatis and M. tuberculosis DNA regions upstream of a reporter gene, we demonstrated the presence of two promoters, pfurA, located immediately upstream of the furA gene, and pkatG, located within the terminal part of the furA coding sequence. Transcription from pfurA was induced upon oxidative stress. A 23-bp sequence overlapping the pfurA -35 region is highly conserved among mycobacteria and streptomycetes and might be involved in controlling pfurA activity. Transcription from a cloned pkatG, lacking the upstream pfurA region, was not induced upon oxidative stress, suggesting a cis-acting regulatory role of this region.
对耻垢分枝杆菌katG上游的DNA区域进行了克隆和测序。在该区域定位到了与结核分枝杆菌furA高度同源的furA基因。furA - katG的基因组织在几种分枝杆菌中似乎是保守的。通过Northern印迹法和引物延伸分析了耻垢分枝杆菌在氧化应激下furA和katG的转录模式。尽管在氧化应激下furA和katG的转录均被诱导,但通过Northern印迹法或逆转录酶PCR均未鉴定出覆盖这两个基因的转录本。分别鉴定出了furA和katG的特异性转录本和5'末端。通过克隆报告基因上游的耻垢分枝杆菌和结核分枝杆菌DNA区域,我们证明了存在两个启动子,即位于furA基因紧上游的pfurA和位于furA编码序列末端部分内的pkatG。氧化应激可诱导pfurA的转录。与pfurA - 35区域重叠的一个23 bp序列在分枝杆菌和链霉菌中高度保守,可能参与控制pfurA的活性。缺乏上游pfurA区域的克隆pkatG的转录在氧化应激下未被诱导,表明该区域具有顺式作用调节功能。