Journal Article

Highly mismatch-tolerant homology testing by RecA could explain how homology length affects recombination

Kleckner, Nancy, Wang, Dianzhuo, Danilowicz, Claudia, Prentiss, Mara, Prévost, Chantal, Fu, Jonathan, Godoy-Carter, Veronica

2023

Overview

In E . coli , double strand breaks (DSBs) are resected and loaded with RecA protein. The genome is then rapidly searched for a sequence that is homologous to the DNA flanking the DSB. Mismatches in homologous partners are rare, suggesting that RecA should rapidly reject mismatched recombination products; however, this is not the case. Decades of work have shown that long lasting recombination products can include many mismatches. In this work, we show that in vitro RecA forms readily observable recombination products when 16% of the bases in the product are mismatched. We also consider various theoretical models of mismatch-tolerant homology testing. The models test homology by comparing the sequences of L test bases in two single-stranded DNAs (ssDNA) from the same genome. If the two sequences pass the homology test, the pairing between the two ssDNA becomes permanent. Stringency is the fraction of permanent pairings that join ssDNA from the same positions in the genome. We applied the models to both randomly generated genomes and bacterial genomes. For both randomly generated genomes and bacterial genomes, the models show that if no mismatches are accepted stringency is ∼ 99% when L test = 14 bp. For randomly generated genomes, stringency decreases with increasing mismatch tolerance, and stringency improves with increasing L test . In contrast, in bacterial genomes when L test ∼ 75 bp, stringency is ∼ 99% for both mismatch-intolerant and mismatch-tolerant homology testing. Furthermore, increasing L test does not improve stringency because most incorrect pairings join different copies of repeats. In sum, for bacterial genomes highly mismatch tolerant homology testing of 75 bp provides the same stringency as homology testing that rejects all mismatches and testing more than ∼75 base pairs is not useful. Interestingly, in vivo commitment to recombination typically requires homology testing of ∼ 75 bp, consistent with highly mismatch intolerant testing.

• Publisher: Public Library of Science,Public Library of Science (PLoS)
• Subject: Analysis / Bacteria / Base Pairing / Biochemistry, Molecular Biology / Biology and Life Sciences / Deoxyribonucleic acid / DNA / DNA, Single-Stranded - genetics / Double-strand break repair / E coli / Escherichia coli - genetics / Escherichia coli - metabolism / Genomes / Genomics / Health aspects / Homology / Homology (Biology) / In vivo methods and tests / Kinases / Life Sciences / Medicine and Health Sciences / Modelling / Nucleotide sequence / Physical sciences / Probability / Rec A Recombinases - genetics / Rec A Recombinases - metabolism / RecA protein / RecA proteins / Recombination / Recombination, Genetic / Research and Analysis Methods / Triplets