ArticleNucleic acids research2026
Collective interactions along recombinase-bound D-loops could speed repair of double-strand breaks by destabilizing flanking homoduplex tails.
Article in Nucleic acids research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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Abstract
During repair of double-strand breaks, recombinases form D-loops in which one strand of the broken chromosome base pairs with a strand from an unbroken chromosome. Thus, the double-stranded DNA (dsDNA) in the unbroken chromosome must melt. Rapid repair requires quick melting. In this work, we present experimental results suggesting that both RecA and ScDmc1 form D-loops that distort the structure of long homoduplex tails in regions adjacent to recombinase-bound D-loops. The observed distortion is not simply due to attempted D-loop extension, but it is consistent with local melting of homoduplex tail regions adjacent to recombinase-bound D-loops. Our experiments indicate that the distortion arises from a collective interaction involving torsional stress that extends along RecA-bound D-loops from one homoduplex tail to the other. Furthermore, molecular dynamics simulations show melting in homoduplex tail regions adjacent to RecA-bound D-loops. Finally, we speculate that the destabilization in the base pairing in homoduplex tails flanking D-loops facilitates the extension of D-loops and underlies the previously observed extension of D-loops through 10 contiguous heterologous bases.
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