Evidence for a Four-Strand Exchange Catalyzed by the RecA Protein
- 10 November 2000
- journal article
- Published by American Chemical Society (ACS) in Biochemistry
- Vol. 39 (49) , 15272-15281
- https://doi.org/10.1021/bi001704o
Abstract
Strand exchange between two duplexes is usually initiated as a three-strand event that requires the presence of a single-stranded overhang or gap in one of the two molecules. Here we show that the RecA protein can catalyze a four-strand exchange. Specifically, it can recombine short hairpin substrates with homologous stems provided that one of the hairpins possesses a chimeric DNA/RNA backbone. This four-strand exchange reaction goes to completion in the presence of ATPγS and releases a stable heteroduplex upon removal of the RecA protein. Under identical conditions, strand exchange between two DNA hairpins is incomplete and generates a nascent heteroduplex that rapidly dissociates when the RecA protein is denatured. Since presynaptic filament formation does not appear to melt either type of hairpin, we propose that exchange occurs between homologously aligned duplexes that are extended and unwound within a RecA filament. The first reaction provides a mechanism for gene targeting by chimeric double-hairpin oligonucleotides while the second reaction explains the ability of the RecA protein to transiently align double-stranded DNA molecules.Keywords
This publication has 11 references indexed in Scilit:
- Helicases as nucleic acid unwinding machines.Nature Structural & Molecular Biology, 2000
- A Molecular Model for RecA-Promoted Strand Exchange via Parallel Triple-Stranded HelicesBiophysical Journal, 1999
- The simultaneous binding of two double-stranded DNA molecules by Escherichia coli RecA proteinJournal of Molecular Biology, 1999
- Targeted gene repairGene Therapy, 1999
- Kinetic Analysis of Pairing and Strand Exchange Catalyzed by RecAJournal of Biological Chemistry, 1997
- Complement-stabilized D-loop: RecA-catalyzed Stable Pairing of Linear DNA Molecules at Internal SitesJournal of Molecular Biology, 1993
- Dissociation pathway for recA nucleoprotein filaments formed on linear duplex DNAJournal of Molecular Biology, 1989
- Binding stoichiometry and structure of RecA-DNA complexes studied by flow linear dichroism and fluorescence spectroscopyJournal of Molecular Biology, 1989
- Structure of helical RecA-DNA complexesJournal of Molecular Biology, 1986
- Characterization of complexes between recA protein and duplex DNA by electron microscopyJournal of Molecular Biology, 1982