N-methyladenine modification of DNA enhances RecA-mediated homologous recombination.

Both DNA methylation and homologous recombination (HR) are extensively studied. In bacteria, Dam methylation is the most studied DNA modification, while RecA-mediated HR is a primary mechanism to repair DNA damages including double-stranded breaks, single-stranded gaps, and stalled replication forks. While HR regulation by proteins is extensively studied, whether methylation of DNA itself directly affects the functions of RecA and HR remains unclear. Mainly by single-molecule experiments, we report that Dam methylation of single-stranded DNA (ssDNA) promotes RecA assembly, partially by reducing the effective charge of ssDNA under counterion screening. Furthermore, Dam methylation of double-stranded DNA promotes homologous pairing, joint molecule growth, and strand exchange. In cellular experiments, deletion impairs HR, whereas hypermethylation of the adenines in the genome enhances HR in P1 transduction assays and DNA-damage sensitivity tests without significantly upregulated HR-related genes. In addition, the preference of RecA for Dam-methylated DNA in RecA assembly and homologous pairing is conserved across divergent species covering a gram-negative bacterium , a gram-positive bacterium and a flowering plant . Dam methylation of ssDNA increases the ATPase activity of molecular motors such as RecQ helicase that containing RecA-like domains. These findings reveal effects of DNA methylation and mechanisms regulating RecA-mediated HR and molecular motors.