4.8 Article

Determination of the two-component systems regulatory network reveals core and accessory regulations across Pseudomonas aeruginosa lineages

Journal

NUCLEIC ACIDS RESEARCH
Volume 49, Issue 20, Pages 11476-11490

Publisher

OXFORD UNIV PRESS
DOI: 10.1093/nar/gkab928

Keywords

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Funding

  1. French National Research Agency (ANR) [ANR-15-IDEX02]
  2. ANR [ANR-15-CE11-0018-01]
  3. Laboratory of Excellence GRAL within the Grenoble Alpes University Graduate School (Ecoles Universitaires de Recherche) CBH-EUR-GS [ANR-17-EURE-0003]
  4. Fondation pour la Recherche Medicale [TeamFRM2017] [DEQ20170336705]
  5. French Ministry of Education and Research
  6. ANR

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Pseudomonas aeruginosa possesses a complex bacterial regulatory network, with approximately half of its detected targets specific to only one or two strains, demonstrating a large functional diversity of transcription factors within a single species. Mechanisms such as differences in accessory genome content and potential auto-regulation or RR-RR cross-regulation were found to be driving this diversity.
Pseudomonas aeruginosa possesses one of the most complex bacterial regulatory networks, which largely contributes to its success as a pathogen. However, most of its transcription factors (TFs) are still uncharacterized and the potential intra-species variability in regulatory networks has been mostly ignored so far. Here, we used DAP-seq to map the genome-wide binding sites of all 55 DNA-binding two-component systems (TCSs) response regulators (RRs) across the three major P. aeruginosa lineages. The resulting networks encompass about 40% of all genes in each strain and contain numerous new regulatory interactions across most major physiological processes. Strikingly, about half of the detected targets are specific to only one or two strains, revealing a previously unknown large functional diversity of TFs within a single species. Three main mechanisms were found to drive this diversity, including differences in accessory genome content, as exemplified by the strain-specific plasmid in IHMA87 outlier strain which harbors numerous binding sites of conserved chromosomally-encoded RRs. Additionally, most RRs display potential auto-regulation or RR-RR cross-regulation, bringing to light the vast complexity of this network. Overall, we provide the first complete delineation of the TCSs regulatory network in P. aeruginosa that will represent an important resource for future studies on this pathogen.

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