Krásný L, Vacík T, Fucík V, Jonák J
Department of Protein Biosynthesis, Institute of Molecular Genetics, Academy of Sciences of the Czech Republic, 166 37 Prague 6, Czech Republic.
J Bacteriol. 2000 Nov;182(21):6114-22. doi: 10.1128/JB.182.21.6114-6122.2000.
The complete primary structure of the str operon of Bacillus stearothermophilus was determined. It was established that the operon is a five-gene transcriptional unit: 5'-ybxF (unknown function; homology to eukaryotic ribosomal protein L30)-rpsL (S12)-rpsG (S7)-fus (elongation factor G [EF-G])-tuf (elongation factor Tu [EF-Tu])-3'. The main operon promoter (strp) was mapped upstream of ybxF, and its strength was compared with the strength of the tuf-specific promoter (tufp) located in the fus-tuf intergenic region. The strength of the tufp region to initiate transcription is about 20-fold higher than that of the strp region, as determined in chloramphenicol acetyltransferase assays. Deletion mapping experiments revealed that the different strengths of the promoters are the consequence of a combined effect of oppositely acting cis elements, identified upstream of strp (an inhibitory region) and tufp (a stimulatory A/T-rich block). Our results suggest that the oppositely adjusted core promoters significantly contribute to the differential expression of the str operon genes, as monitored by the expression of EF-Tu and EF-G.
嗜热脂肪芽孢杆菌str操纵子的完整一级结构已被确定。已确定该操纵子是一个五基因转录单元:5'-ybxF(功能未知;与真核核糖体蛋白L30同源)-rpsL(S12)-rpsG(S7)-fus(延伸因子G [EF-G])-tuf(延伸因子Tu [EF-Tu])-3'。主要操纵子启动子(strp)被定位在ybxF上游,并将其强度与位于fus-tuf基因间区域的tuf特异性启动子(tufp)的强度进行了比较。在氯霉素乙酰转移酶测定中确定,tufp区域启动转录的强度比strp区域高约20倍。缺失定位实验表明,启动子强度不同是由位于strp上游(一个抑制区域)和tufp上游(一个富含A/T的刺激区域)的反向作用顺式元件共同作用的结果。我们的结果表明,如通过EF-Tu和EF-G的表达所监测到的,反向调节的核心启动子对str操纵子基因的差异表达有显著贡献。