ArticleFrontiers in cellular and infection microbiology2025
Transcriptomic and proteomic profiling of
Article in Frontiers in cellular and infection microbiology, 2025. 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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1 citing paper in PubMed.
- AnResearch square · 2026Article
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6 authors.
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Abstract
Background: Methods: An integrated analysis combining transcriptomic and proteomic profiling was employed to detect genetic and protein changes in APP under iron starvation. Results: In total, 458 differentially expressed genes (DEGs) from the transcriptome and 532 differentially expressed proteins (DEPs) from the proteome were identified. The comparative analysis showed that 137 differentially expressed genes/proteins were shared between DEGs and DEPs, with the majority exhibiting consistent regulatory changes at both transcription and protein levels. Functional enrichment analysis revealed that the downregulated genes were predominantly associated with the generation of precursor metabolites and energy (45/105, 42.86%), primary metabolic process (29/105, 27.62%), ion binding (20/105, 19.05%), and metal cluster binding (18/105, 17.14%), corresponding to pathways involved in primary metabolites and energy biosynthesis and cellular respiration. Conversely, the upregulated genes were primarily enriched in iron transport (11/30, 36.67%) and iron binding (9/30, 30%), which corresponded to the iron starvation conditions. The expression changes of iron utilization systems, including TonB-ExbB-ExbD and some TonB-dependent receptors, by qRT-PCR were consistent with the results in both transcriptome and proteome analyses. Conclusion: This study provided a global perspective on the response mechanisms employed by APP to iron starvation, characterized by suppressing electron transport and energy metabolism pathways and upregulating the pathways associated with the TonB-ExbB-ExbD energy transduction system for iron acquisition.
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