DprA recruits ComM to facilitate recombination during natural transformation in Gram-negative bacteria
Abstract
Natural transformation (NT) represents one of the major modes of horizontal gene transfer in bacterial species. During NT, cells can take up free DNA from the environment and integrate it into their genome by homologous recombination. While NT has been studied for >90 y, the molecular details underlying this recombination remain poorly understood. Recent work has demonstrated that ComM is an NT-specific hexameric helicase that promotes recombinational branch migration in Gram-negative bacteria. How ComM is loaded onto the postsynaptic recombination intermediate during NT, however, remains unclear. Another NT-specific recombination mediator protein that is ubiquitously conserved in both Gram-positive and Gram-negative bacteria is DprA. Here, we uncover that DprA homologs in Gram-negative species contain a C-terminal winged helix domain that is predicted to interact with ComM by AlphaFold. Using Helicobacter pylori and Vibrio cholerae as model systems, we demonstrate that ComM directly interacts with the DprA winged-helix domain, and that this interaction is critical for DprA to recruit ComM to the recombination site to promote branch migration during NT. These results advance our molecular understanding of recombination during this conserved mode of horizontal gene transfer. Furthermore, they demonstrate how structural modeling can help uncover unexpected interactions between well-studied proteins to provide deep mechanistic insight into the molecular coordination required for their activity.
Article Details
Journal Info
Proceedings of the National Academy of Sciences
National Academy of Sciences
Authors (8)
Triana N. Dalia
Department of Biology, Indiana University
Mérick Machouri
Université Paris-Saclay, iRCM/IBFJ, CEA, Genetic Stability, Stem Cells and Radiation
Céline Lacrouts
Université Paris-Saclay, iRCM/IBFJ, CEA, Genetic Stability, Stem Cells and Radiation
Yoann Fauconnet
Université Paris-Saclay, Commissariat à l’Energie Atomique, CNRS, Institute for Integrative Biology of the Cell
Raphaël Guérois
Jessica Andreani
J. Pablo Radicella
Université Paris-Saclay, Institut de Biologie François Jacob/Institut de Radiobiologie Cellulaire et Moléculaire, Commissariat à l’Energie Atomique, Genetic Stability, Stem Cells and Radiation
Ankur B. Dalia
Department of Biology, Indiana University