Single-molecule DNA repair in live bacteria.

Journal article

Cellular DNA damage is reversed by balanced repair pathways that avoid accumulation of toxic intermediates. Despite their importance, the organization of DNA repair pathways and the function of repair enzymes in vivo have remained unclear because of the inability to directly observe individual reactions in living cells. Here, we used photoactivation, localization, and tracking in live Escherichia coli to directly visualize single fluorescent labeled DNA polymerase I (Pol) and ligase (Lig) molecules searching for DNA gaps and nicks, performing transient reactions, and releasing their products. Our general approach provides enzymatic rates and copy numbers, substrate-search times, diffusion characteristics, and the spatial distribution of reaction sites, at the single-cell level, all in one measurement. Single repair events last 2.1 s (Pol) and 2.5 s (Lig), respectively. Pol and Lig activities increased fivefold over the basal level within minutes of DNA methylation damage; their rates were limited by upstream base excision repair pathway steps. Pol and Lig spent >80% of their time searching for free substrates, thereby minimizing both the number and lifetime of toxic repair intermediates. We integrated these single-molecule observations to generate a quantitative, systems-level description of a model repair pathway in vivo.

Authors: Uphoff, S; Reyes-Lamothe, R; Garza de Leon, F; Sherratt, D; Kapanidis, A

• Publication status: Published
• Journal: Proceedings of the National Academy of Sciences of the United States of America
• Volume: 110
• Issue: 20
• Pages: 8063-8068
• Publication date: 2013-05-01
• DOI: 10.1073/pnas.1301804110
• EISSN: 1091-6490
• ISSN: 0027-8424
• Language: English
• Keywords: Diffusion; DNA Repair; DNA-Directed DNA Polymerase; Cytosol; DNA Damage; Substrate Specificity; Microscopy, Fluorescence; Bacteria; Escherichia coli; DNA Methylation; Protein Binding