4.7 Article

Machine-learning from Pseudomonas putida KT2440 transcriptomes reveals its transcriptional regulatory network

Journal

METABOLIC ENGINEERING
Volume 72, Issue -, Pages 297-310

Publisher

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.ymben.2022.04.004

Keywords

Machine learning; Independent component analysis; Transcriptome; Systems biology; Pseudomonas putida

Funding

  1. Office of Science, Office of Biological and Environmental Research, of the U.S. Department of Energy (DOE) [DE-AC02-05CH11231]
  2. U.S. DOE [DE-AC05-00OR22725, DE-AC36-08GO28308]
  3. U.S. DOE Office of Energy Efficiency and Renewable Energy Bioenergy Technologies Office (BETO)
  4. Nebraska Center for Energy Science Research at the University of Nebraska - Lincoln

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This study applies a machine-learning approach to uncover the genome-scale transcriptional regulatory network in Pseudomonas putida KT2440, providing a basis for understanding its physiological processes and engineering it for practical use.
Bacterial gene expression is orchestrated by numerous transcription factors (TFs). Elucidating how gene expression is regulated is fundamental to understanding bacterial physiology and engineering it for practical use. In this study, a machine-learning approach was applied to uncover the genome-scale transcriptional regulatory network (TRN) in Pseudomonas putida KT2440, an important organism for bioproduction. We performed independent component analysis of a compendium of 321 high-quality gene expression profiles, which were previously published or newly generated in this study. We identified 84 groups of independently modulated genes (iModulons) that explain 75.7% of the total variance in the compendium. With these iModulons, we (i) expand our understanding of the regulatory functions of 39 iModulon associated TFs (e.g., HexR, Zur) by systematic comparison with 1993 previously reported TF-gene interactions; (ii) outline transcriptional changes after the transition from the exponential growth to stationary phases; (iii) capture group of genes required for utilizing diverse carbon sources and increased stationary response with slower growth rates; (iv) unveil multiple evolutionary strategies of transcriptome reallocation to achieve fast growth rates; and (v) define an osmotic stimulon, which includes the Type VI secretion system, as coordination of multiple iModulon activity changes. Taken together, this study provides the first quantitative genome-scale TRN for P. putida KT2440 and a basis for a comprehensive understanding of its complex transcriptome changes in a variety of physiological states.

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