DprA recruits ComM to facilitate recombination during natural transformation in Gram-negative bacteria

T Triana N. Dalia (Department of Biology, Indiana University) M Mérick Machouri (Université Paris-Saclay, iRCM/IBFJ, CEA, Genetic Stability, Stem Cells and Radiation) C Céline Lacrouts (Université Paris-Saclay, iRCM/IBFJ, CEA, Genetic Stability, Stem Cells and Radiation) Y Yoann Fauconnet (Université Paris-Saclay, Commissariat à l’Energie Atomique, CNRS, Institute for Integrative Biology of the Cell) R Raphaël Guérois J Jessica Andreani J 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) A Ankur B. Dalia (Department of Biology, Indiana University)

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

Volume / Issue Vol. 122, Issue 15
Published April 15, 2025
ISSN 0027-8424
Publisher National Academy of Sciences

Authors (8)

T

Triana N. Dalia

Department of Biology, Indiana University

M

Mérick Machouri

Université Paris-Saclay, iRCM/IBFJ, CEA, Genetic Stability, Stem Cells and Radiation

C

Céline Lacrouts

Université Paris-Saclay, iRCM/IBFJ, CEA, Genetic Stability, Stem Cells and Radiation

Y

Yoann Fauconnet

Université Paris-Saclay, Commissariat à l’Energie Atomique, CNRS, Institute for Integrative Biology of the Cell

R

Raphaël Guérois

J

Jessica Andreani

J

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

A

Ankur B. Dalia

Department of Biology, Indiana University