Abstract
The plasmid gene cat-86 specifies chloramphenicol-inducible, chloramphenicol acetyltransferase in Bacillus subtilis. The inducible regulation is independent of the promoter that is used to activate cat-86 and is independent of the cat-86 coding sequence. We have proposed that the regulation of cat-86 results from the transcription of a pair of inverted-repeat sequences that immediately precede the coding sequence. These transcripts are predicted to sequester the cat-86 ribosome binding site in a stable RNA stem-loop which, in theory, should block the ribosome binding site from pairing with 16S rRNA. Inducible expression of cat-86 may therefore result in part from regulation of the translation of cat-86 mRNA. However, chloramphenicol-induction correlates with increased levels of cat-86 mRNA and the RNA stem-loop preceding the cat-86 coding sequence structurally resembles a rho-independent transcription terminator. We have therefore tested the inverted-repeats as a potential site of transcription termination. Transcription studies performed in vitro using SP6 RNA polymerase and in vivo by S1 mapping demonstrate that a substantial fraction of the potential cat-86 transcripts terminate at a site immediately 3' to the inverted-repeats. The results of the in vivo experiments suggest that the termination signal may be partially relieved by growth of cells in chloramphenicol.
MeSH Terms
Acetyltransferases/genetics
Bacillus subtilis/genetics
Base Sequence
Chloramphenicol/pharmacology
Chloramphenicol O-Acetyltransferase
DNA-Directed RNA Polymerases/genetics
Enzyme Induction
Gene Expression Regulation/drug effects
Genes, Bacterial
Genes, Regulator
Nucleic Acid Conformation
Plasmids
Promoter Regions, Genetic
Transcription, Genetic/drug effects
Chemicals
Chloramphenicol
Acetyltransferases
Chloramphenicol O-Acetyltransferase
DNA-Directed RNA Polymerases
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Ambulos N P
Mongkolsuk S
Lovett P S
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18 references, click to expand
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