COMPARATIVE-ANALYSIS OF THE CYA LOCUS IN ENTEROBACTERIA AND RELATED GRAM-NEGATIVE FACULTATIVE ANAEROBES

Citation
P. Trotot et al., COMPARATIVE-ANALYSIS OF THE CYA LOCUS IN ENTEROBACTERIA AND RELATED GRAM-NEGATIVE FACULTATIVE ANAEROBES, Biochimie, 78(4), 1996, pp. 277-287
Citations number
39
Categorie Soggetti
Biology
Journal title
ISSN journal
03009084
Volume
78
Issue
4
Year of publication
1996
Pages
277 - 287
Database
ISI
SICI code
0300-9084(1996)78:4<277:COTCLI>2.0.ZU;2-T
Abstract
Comparison of the cya loci (cya codes for adenylyl cyclase (AC)) from a variety of phylogenetically divergent facultative anaerobic Gram-neg ative bacteria reveals conserved sequence features. The entire locus s tructure in enterobacteria is preserved, including two major promoters (a conserved cya strong promoter, P2, and a divergent promoter for a heme biosynthetic operon, hemCD) present in the upstream region of the cya gene. The region between hemC and cya is much longer in Proteus m irabilis than in other enterobacteria, and lacks the P1 upstream cya p romoter. In Aeromonas hydrophila the cya promoter (the strong P2 promo ter in E coli) is preserved, including a putative GATC methylation sit e situated immediately downstream from the -10 box. Each cya frame ana lyzed uses TTG as the translation start codon and is preceded by an un usual ribosome binding site. This suggests that a lower translation ef ficiency of the cya transcript could be the result of some selection p ressure. This has been substantiated by in vitro mutagenesis and by se lection of up mutations which all map at the cya ribosome binding site . In enterobacteria the cyaY frame is the only conserved reading frame downstream of cya, with the orientation opposite to that of cya. This organization is not preserved in Aeromonas. Experiments involving fus ions with the lacZ gene demonstrated that cyaY is expressed. Finally, comparison of the different polypeptide sequences of ACs permits discu ssion of important features of the catalytic and regulatory centers of the protein.