Abstract
The initiation sites of transcription in vivo for the three genes caa, cai and cal encoding respectively colicin A (Caa), the immunity protein (Cai) and the pColA lysis protein (Cal) have been analysed by nuclease S1 mapping. This analysis demonstrates that caa and cal form an operon. cai is located between these two genes and transcribed in the opposite direction from its own promoter. The start sites for caa and cai have also been determined in vitro. For caa, the same start site was found in vivo and in vitro. In contrast, for cai the most efficient start site in vitro was not used in vivo. LexA protein strongly repressed the in vivo and in vitro transcription of the caa-cal operon. As determined by DNase 1 protection experiments, LexA protein binds with a high affinity to an approximately 40 bp long sequence just downstream of the Pribnow box. The sequence of the binding site is composed of two overlapped "SOS boxes". Two transcripts of the caa-cal operon were detected by blot hybridization. The longer mRNA can direct the synthesis of both Caa and Cal while the shorter one is terminated at the end of caa. When the transcription of the caa-cal operon is induced, there is a strong interference with cai transcription.
MeSH Terms
Bacterial Proteins/genetics
Bacteriocin Plasmids
Colicins/genetics
DNA, Recombinant
Gene Expression Regulation
Genes, Bacterial
Operator Regions, Genetic
Operon
Plasmids
Promoter Regions, Genetic
RNA, Bacterial/genetics
RNA, Messenger/genetics
Serine Endopeptidases
Transcription, Genetic
Chemicals
Bacterial Proteins
Colicins
DNA, Recombinant
LexA protein, Bacteria
RNA, Bacterial
RNA, Messenger
Serine Endopeptidases
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Lloubes R
Baty D
Lazdunski C
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24 references, click to expand
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