ArticleNature communications2026
Characterization of hypothetical proteins reveals function modules and virulence factors in Pseudomonas aeruginosa.
Article in Nature communications, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Who cites it
1 citing paper in PubMed.
- Characterization of hypothetical proteins reveals function modules and virulence factors in Pseudomonas aeruginosa.Nature communications · 2026Article
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18 authors.
Funding
Abstract
Hypothetical proteins (HPs), known as biological dark matter, are genetic sequences of which the biological functions and regulatory processes remain largely unclear. In Pseudomonas aeruginosa, HPs account for 36.4% of all coding genes, representing a significant gap in understanding their functions and contribution to the virulence network. To address these challenges, we present a deletion repertoire comprising 938 strains targeting 1165 HPs in P. aeruginosa. Starting with transcriptome-wide analysis, we inferred putative functional predictions for HP mutants through systematic profiling of differential expression and candidate transcriptional pathways. We integrated our expression profiles with public datasets (5707 genes × 2312 conditions). This allowed us to distinguish constitutively expressed genes from variable genes. Using independent component analysis (ICA), we identified 56 independent regulatory Modules, providing a comprehensive transcriptional-association framework. These contributed to the discovery and experimental validation of 20 virulence-related hypothetical proteins (VRHPs) and 3 antibiotic resistance-related hypothetical proteins (ARHPs). Evolutionary analysis across bacterial taxa provided additional insights into HP sequence conservation and evolutionary dynamics. In summary, our study presents a large-scale HP mutant library combined with integrated transcriptomic and machine learning approaches, establishing both a valuable resource and a systematic strategy for predicting and prioritizing candidate functions of HPs across bacterial species.
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