| Literature DB >> 35976223 |
Mark A Zaydman1, Arjun S Raman2,3,4, Alexander S Little2, Fidel Haro2, Valeryia Aksianiuk2, William J Buchser5, Aaron DiAntonio6, Jeffrey I Gordon1,7, Jeffrey Milbrandt5.
Abstract
Cellular behaviors emerge from layers of molecular interactions: proteins interact to form complexes, pathways, and phenotypes. We show that hierarchical networks of protein interactions can be defined from the statistical pattern of proteome variation measured across thousands of diverse bacteria and that these networks reflect the emergence of complex bacterial phenotypes. Our results are validated through gene-set enrichment analysis and comparison to existing experimentally derived databases. We demonstrate the biological utility of our approach by creating a model of motility in Pseudomonas aeruginosa and using it to identify a protein that affects pilus-mediated motility. Our method, SCALES (Spectral Correlation Analysis of Layered Evolutionary Signals), may be useful for interrogating genotype-phenotype relationships in bacteria.Entities:
Keywords: Pseudomonas aeruginosa; complexity; computational biology; emergence; hierarchy; physics of living systems; protein interaction networks; proteome; systems biology
Mesh:
Substances:
Year: 2022 PMID: 35976223 PMCID: PMC9427106 DOI: 10.7554/eLife.74104
Source DB: PubMed Journal: Elife ISSN: 2050-084X Impact factor: 8.713