Hutchings M I, Drabble W T
Division of Biochemistry and Molecular Biology, School of Biological Sciences, University of Southampton, Biomedical Sciences Building, Bassett Crescent East, SO16 7PX, Southampton, UK.
FEMS Microbiol Lett. 2000 Jun 15;187(2):115-22. doi: 10.1111/j.1574-6968.2000.tb09146.x.
The gua promoter (guaP) of Escherichia coli resembles those for ribosomal RNA (rrn) operons and lies in a close back-to-back arrangement with the promoter for xseA (xseP). Transcription from guaP is subject to stringent control and growth-rate-dependent regulation, and to repression by DnaA and PurR. In addition, transcription from guaP is regulated by the cyclic AMP receptor protein (CRP). Plasmid-borne promoter fusions to the receptor gene for chloramphenicol acetyl transferase were used to assess the role of CRP in controlling transcription from guaP and xseP following a downshift of cultures from rich into minimal medium. CRP is required to activate guaBA transcription and repress xseA transcription following downshift. Bandshift assays with a DNA fragment carrying the divergent promoters revealed specific binding of CRP. We propose that CRP, binding to a near-consensus site centred at -117.5, activates transcription from guaP and obstructs transcription from the xseA promoter.
大肠杆菌的gua启动子(guaP)类似于核糖体RNA(rrn)操纵子的启动子,与xseA(xseP)的启动子紧密背靠背排列。guaP的转录受到严格控制和生长速率依赖性调节,并受到DnaA和PurR的抑制。此外,guaP的转录受环腺苷酸受体蛋白(CRP)调节。将携带氯霉素乙酰转移酶受体基因的质粒启动子融合体用于评估CRP在培养物从丰富培养基转入基本培养基后下调时控制guaP和xseP转录中的作用。下调后,需要CRP来激活guaBA转录并抑制xseA转录。用携带不同启动子的DNA片段进行的凝胶迁移实验揭示了CRP的特异性结合。我们提出,CRP结合到以-117.5为中心的近共有位点,激活guaP的转录并阻碍xseA启动子的转录。