Involvement of Escherichia coli FIS protein in maintenance of bacteriophage Mu lysogeny by the repressor : control of early transcription and inhibition of transposition

Autor: Michael Chandler, I Poquet, Mireille Bétermier, Robert Alazard
Přispěvatelé: Centre National de la Recherche Scientifique (CNRS)
Jazyk: angličtina
Rok vydání: 1993
Předmět:
Transcription
Genetic

Operon
phage lambda
Regulatory Sequences
Nucleic Acid

medicine.disease_cause
Bacteriophage
lac repressor
Factor For Inversion Stimulation Protein
Genetics
0303 health sciences
biology
Escherichia coli Proteins
DNA-Binding Proteins
[SDV.MP]Life Sciences [q-bio]/Microbiology and Parasitology
Oligodeoxyribonucleotides
Bacteriophage Mu
Protein Binding
Research Article
binding-site
Integration Host Factors
ends
dna-sequences
Blotting
Western

Molecular Sequence Data
cloning vehicles
Repressor
Microbiology
Bacteriophage mu
03 medical and health sciences
Lysogenic cycle
Consensus Sequence
expression
Escherichia coli
medicine
RNA
Messenger

gene
Lysogeny
Molecular Biology
Prophage
030304 developmental biology
Base Sequence
030306 microbiology
Genetic Complementation Test
Gene Expression Regulation
Bacterial

biology.organism_classification
Repressor Proteins
integration host factor
DNA Transposable Elements
Mutagenesis
Site-Directed

Carrier Proteins
strand-transfer-reaction
Zdroj: Journal of Bacteriology
Journal of Bacteriology, American Society for Microbiology, 1993, 175 (12), pp.3798-3811. ⟨10.1128/jb.175.12.3798-3811.1993⟩
Scopus-Elsevier
ISSN: 0021-9193
1098-5530
Popis: International audience; The Escherichia coli FIS (factor for inversion stimulation) protein has been implicated in assisting bacteriophage Mu repressor, c, in maintaining the lysogenic state under certain conditions. In a fis strain, a temperature-inducible Mucts62 prophage is induced at lower temperatures than in a wild-type host (M. Bétermier, V. Lefrère, C. Koch, R. Alazard, and M. Chandler, Mol. Microbiol. 3:459-468, 1989). Increasing the prophage copy number rendered Mucts62 less sensitive to this effect of the fis mutation, which thus seems to depend critically on the level of repressor activity. The present study also provides evidence that FIS affects the control of Mu gene expression and transposition. As judged by the use of lac transcriptional fusions, repression of early transcription was reduced three- to fourfold in a fis background, and this could be compensated by an increase in cts62 gene copy number. c was also shown to inhibit Mu transposition two- to fourfold less strongly in a fis host. These modulatory effects, however, could not be correlated to sequence-specific binding of FIS to the Mu genome, in particular to the strong site previously identified on the left end. We therefore speculate that a more general function of FIS is responsible for the observed modulation of Mu lysogeny.
Databáze: OpenAIRE