Characterization of a Mutant RecA Protein that Facilitates Homologous Genetic Recombination but not Recombinational DNA Repair: RecA423

• Published in: Journal of molecular biology 1996-12, Vol.264 (4), p.696-712
• Main Authors: Ishimori, Koichiro, Sommer, Suzanne, Bailone, Adriana, Takahashi, Masayuki, Cox, Michael M., Devoret, Raymond
• Format: Article
• Language: English
• Subjects: Adenosine Triphosphatases - metabolism; Adenosine Triphosphate - metabolism; Base Composition; Conjugation, Genetic; DNA Damage; DNA Repair; DNA Replication; DNA, Bacterial - metabolism; DNA, Single-Stranded - metabolism; Escherichia coli; Escherichia coli - genetics; Escherichia coli - metabolism; Genotype; homologous recombination; Phenotype; Point Mutation; Rec A Recombinases - genetics; Rec A Recombinases - metabolism; RecA protein; RecA – DNA complex; Recombination, Genetic; replication restart; Sodium Chloride - pharmacology; SOS Response (Genetics); Transduction, Genetic; Ultraviolet Rays
• ISSN: 0022-2836; 1089-8638
• DOI: 10.1006/jmbi.1996.0670

A recAmutant ( recA423; Arg 169→ His), with properties that should help clarify the relationship between the biochemical properties of RecA protein and its two major functions, homologous genetic recombination and recombinational DNA repair, has been isolated. The mutant has been characterized in vivoand the purified RecA423 protein has been studied in vitro. The recA423cells are nearly as proficient in conjugational recombination, transductional recombination, and recombination of I red − gam −phage as wild-type cells. At the same time, the mutant cells are deficient for intra-chromosomal recombination and nearly as sensitive to UV irradiation as a recAdeletion strain. The cells are proficient in SOS induction, and results indicate the defect involves the capacity of RecA protein to participate directly in recombinational DNA repair. In vitro, the RecA423 protein binds to single-stranded DNA slowly, with an associated decline in the ATP hydrolytic activity. The RecA423 protein promoted a limited DNA strand exchange reaction when the DNA substrates were homologous, but no bypass of a short heterologous insert in the duplex DNA substrate was observed. These results indicate that poor binding to DNA and low ATP hydrolysis activity can selectively compromise certain functions of RecA protein. The RecA423 protein can promote recombina tion between homologous DNAs during Hfr crosses, indicating that the biochemical requirements for such genetic exchanges are minimal. However, the deficiencies in recombinational DNA repair suggest that the biochemical requirements for this function are more exacting.