Activation of transcription at specific promoters by glycerol.

Glycerol added to a transcription system containing Xgal DNA and Escherichia coli RNA polymerase holoenzyme stimulates total RNA synthesis and replaces the requirement for cyclic adenosine 3’:5’-monophosphate (CAMP) and CAMP receptor (CRP) for promotion of gal RNA synthesis. The stimulatory effect which is proportional to the concentration of glycerol up to 20% (v/v) occurs at the level of preinitiation complex formation. In stimulating gal transcription, glycerol appears to act at or close to the same site as CAMP and CRP because: (a) glycerol has little effect on gal transcription at saturating levels of CAMP and CRP; (b) although glycerol stimulates transcription from Xgal DNA bearing revertible gal promoter mutations, transcription from DNA containing a gal promoter deletion is not stimulated; (c) glycerol stimulation of gal promoter mutants is inhibited by CAMP and CRP; and (d) with either glycerol or CAMP and CRP, transcription of the promoter-proximal gaZE region precedes transcription of the gaZKT region. The effect of glycerol on X early transcription is to stimulate early r-strand RNA synthesis but not early Z-strand RNA synthesis. However, if the DNA template contains a defective Xsex promoter, the decreased levels of early Z-strand RNA are restored to normal by glycerol. Ethylene glycol, dimethylsulfoxide, sucrose, and 1,3propanediol, all of which lower the T, of DNA, also stimulate both total RNA and gal RNA synthesis. Furthermore, the glycerol-promoted formation of the gal preinitiation complex is strongly dependent on the preincubation temperature. At lower temperatures, complex formation requires increased glycerol or decreased KC1 concentrations. These findings suggest that glycerol may act by melting or changing the conformation of the DNA promoter regions.