Journal of Biological Chemistry · 2003 · 184 citations · 29 references
Life SciencesGeneticsMolecular BiologyChromatin BiologyDna RepairRecombinationChromatinDna Double-strand Break RepairDouble-strand Break RepairHistone ProteinsHomologous RecombinationRecombination EnzymesAtp-dependent Chromatin RemodelingChromatin RemodelingDna Double-strand BreaksDouble-strand Dna BreaksHeteroduplex Dna FormationHeteroduplex FormationReca Family RecombinasesReca Recombinase
In eukaryotic cells, the repair of DNA double-strand breaks by homologous recombination requires a RecA-like recombinase, Rad51p, and a Swi2p/Snf2p-like ATPase, Rad54p. Here we find that yeast Rad51p and Rad54p support robust homologous pairing between single-stranded DNA and a chromatin donor. In contrast, bacterial RecA is incapable of catalyzing homologous pairing with a chromatin donor. We also show that Rad54p possesses many of the biochemical properties of bona fide ATP-dependent chromatin-remodeling enzymes, such as ySWI/SNF. Rad54p can enhance the accessibility of DNA within nucleosomal arrays, but it does not seem to disrupt nucleosome positioning. Taken together, our results indicate that Rad54p is a chromatin-remodeling enzyme that promotes homologous DNA pairing events within the context of chromatin.
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Molecular cloning: A laboratory manual
Prescott L. Deininger · Analytical Biochemistry · 1990 · 86.2K citations
Richard D. Wood, Michael Mitchell, John Sgouros et al. · Science · 2001 · 1.5K citations