Abstract
We have isolated two spontaneous mutations that increase the expression of the Tn9-derived cat gene in Bacillus subtilis. These mutations, which appear to affect initiation of translation of chloramphenicol acetyltransferase (CAT; acetyl-CoA:chloramphenicol 3-O-acetyltransferase, EC 2.3.1.28) consist of a tandem duplication and triplication of a 55-base-pair sequence located at the 5' end of cat. Included in the repeated sequence are the Shine-Dalgarno site, initiation codon, and a region of dyad symmetry located within the structural portion of the cat gene. A striking feature of the mutated initiation sites is their potential to form stem-loop structures at the 5' end of the cat messenger RNA. Within the single-stranded loops of these structures are the ribosome binding site and initiation codon for the cat gene. It appears that the Gram-negative cat translation initiation site has mutated to permit efficient utilization in B. subtilis without directly affecting Shine-Dalgarno sequence homology. This report suggests that secondary structure in the vicinity of the Shine-Dalgarno site can exert a strong positive influence on the initiation of translation in B. subtilis.
MeSH Terms
Acetyltransferases/genetics
Bacillus subtilis/genetics
Binding Sites
Chloramphenicol O-Acetyltransferase
Chromosome Deletion
DNA Transposable Elements
DNA, Bacterial/genetics
Gene Expression Regulation
Genes, Bacterial
Mutation
Nucleic Acid Conformation
Peptide Chain Initiation, Translational
Promoter Regions, Genetic
Protein Biosynthesis
RNA, Messenger/metabolism
Ribosomes/metabolism
Chemicals
DNA Transposable Elements
DNA, Bacterial
RNA, Messenger
Acetyltransferases
Chloramphenicol O-Acetyltransferase
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Lin C K
Goldfarb D S
Doi R H
Rodriguez R L
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