4.8 Article

Machine learning from Pseudomonas aeruginosa transcriptomes identifies independently modulated sets of genes associated with known transcriptional regulators

Journal

NUCLEIC ACIDS RESEARCH
Volume 50, Issue 7, Pages 3658-3672

Publisher

OXFORD UNIV PRESS
DOI: 10.1093/nar/gkac187

Keywords

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Funding

  1. NIH [U01 AI124316]
  2. Novo Nordisk Foundation [NNF10CC1016517]

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In this study, the transcriptional regulatory network (TRN) of Pseudomonas aeruginosa was reconstructed using 364 transcriptomes, and important gene regulatory modules were identified. The study identified modules that play important physiological roles under different conditions and compared the conservation of regulatory elements between P. aeruginosa and Escherichia coli.
The transcriptional regulatory network (TRN) of Pseudomonas aeruginosa coordinates cellular processes in response to stimuli. We used 364 transcriptomes (281 publicly available + 83 in-house generated) to reconstruct the TRN of P. aeruginosa using independent component analysis. We identified 104 independently modulated sets of genes (iModulons) among which 81 reflect the effects of known transcriptional regulators. We identified iModulons that (i) play an important role in defining the genomic boundaries of biosynthetic gene clusters (BGCs), (ii) show increased expression of the BGCs and associated secretion systems in nutrient conditions that are important in cystic fibrosis, (iii) show the presence of a novel ribosomally synthesized and post-translationally modified peptide (RiPP) BGC which might have a role in P. aeruginosa virulence, (iv) exhibit interplay of amino acid metabolism regulation and central metabolism across different carbon sources and (v) clustered according to their activity changes to define iron and sulfur stimulons. Finally, we compared the identified iModulons of P. aeruginosa with those previously described in Escherichia coli to observe conserved regulons across two Gram-negative species. This comprehensive TRN framework encompasses the majority of the transcriptional regulatory machinery in P. aeruginosa, and thus should prove foundational for future research into its physiological functions.

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