Abstract
The Escherichia coli (Es. coli) protein Fis (factor for inversion stimulation) stimulates site-specific DNA inversion of the G segment in phage Mu by binding to a recombinational enhancer. By using synthetic oligonucleotides deduced from the amino-terminal amino acid sequence, we have cloned the gene (termed fis) encoding this specific DNA-binding protein. The DNA sequence shows that the Fis protein is basic and contains 98 amino acids. A helix-turn-helix sequence motif characteristic of many DNA-binding proteins is located at the carboxyl-terminal end of the protein. By marker exchange, we have constructed an insertion mutation of fis. Fis is nonessential for Es. coli growth; however, inversion of the G segment of a Mu prophage was not detected in the fis mutant. The fis gene is located between 71 and 72 min on the Es. coli genetic map.
MeSH Terms
Amino Acid Sequence
Base Sequence
Carrier Proteins/genetics
Chromosome Inversion
Cloning, Molecular
DNA Restriction Enzymes
DNA, Bacterial/genetics
DNA-Binding Proteins/genetics
Escherichia coli/genetics
Escherichia coli Proteins
Factor For Inversion Stimulation Protein
Genes
Genes, Bacterial
Integration Host Factors
Molecular Sequence Data
Chemicals
Carrier Proteins
DNA, Bacterial
DNA-Binding Proteins
Escherichia coli Proteins
Factor For Inversion Stimulation Protein
Integration Host Factors
integration host factor, E coli
DNA Restriction Enzymes
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Koch C
Max-Planck-Institut für Molekulare Genetik, Otto-Warburg-Laboratorium, Berlin, Federal Republic of Germany.
Vandekerckhove J
Kahmann R
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