Base triplet stepping by the Rad51/RecA family of recombinases

Ja Yil Lee(Columbia University), Tsuyoshi Terakawa(Kyoto University), Zhi Qi(Columbia University), Justin B. Steinfeld(Columbia University), Sy Redding(Columbia University), Youngho Kwon(Yale University), William A. Gaines(Yale University), Weixing Zhao(Yale University), Patrick Sung(Yale University), Eric C. Greene(Howard Hughes Medical Institute)
Science
August 27, 2015
Cited by 181

Abstract

DNA strand exchange plays a central role in genetic recombination across all kingdoms of life, but the physical basis for these reactions remains poorly defined. Using single-molecule imaging, we found that bacterial RecA and eukaryotic Rad51 and Dmc1 all stabilize strand exchange intermediates in precise three-nucleotide steps. Each step coincides with an energetic signature (0.3 kBT) that is conserved from bacteria to humans. Triplet recognition is strictly dependent on correct Watson-Crick pairing. Rad51, RecA, and Dmc1 can all step over mismatches, but only Dmc1 can stabilize mismatched triplets. This finding provides insight into why eukaryotes have evolved a meiosis-specific recombinase. We propose that canonical Watson-Crick base triplets serve as the fundamental unit of pairing interactions during DNA recombination.


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