Beyond Repression: ArsR Functions as a Global Activator of Metabolic and Redox Responses in Escherichia coli

dc.contributor.authorSather, Brett
dc.contributor.authorLarson, James
dc.contributor.authorHutt Vater, Kian
dc.contributor.authorWestrum, Jade
dc.contributor.authorMcDermott, Timothy R.
dc.contributor.authorBothner, Brian
dc.date.accessioned2026-06-23T21:03:31Z
dc.date.issued2026-01
dc.description.abstractBackground: The arsenic-responsive repressor, ArsR, has long been understood as a canonical regulator of the arsRBC operon, which confers resistance to arsenic stress. However, recent studies suggest a broader regulatory scope for ArsR. Here, we investigated the proteomic landscape of Escherichia coli strains with and without ArsR to elucidate ArsR as an activator in both non-stressing and arsenic-stressing conditions. Methods: Using mass-spectrometry-based shotgun proteomics and statistical analyses, we characterized the differential abundance of proteins across AW3110 (ΔarsRBC), AW3110 complemented with arsR, and wild-type K-12 strains under control and arsenite-stressed conditions. Results: Our study shows that ArsR influences proteomic networks beyond the ars operon, integrating metabolic and redox responses crucial for cellular adaptation and survival. This suggests that ArsR has a significant role in gut microbiome metabolomic profiles in response to arsenite. Proteins involved in alanine, lactaldehyde, arginine, thioredoxin, and proline pathways were significantly elevated in strains where ArsR was detected, both with and without arsenite. We identified proteins exhibiting an “ArsR-dependent” activation pattern, highlighting ArsR’s potential role in redox balance and energy metabolism. Conclusions: These findings challenge the classical view of ArsR as a repressor and position it as a pleiotropic regulator, including broad activation.
dc.identifier.citationSather B, Larson J, Hutt Vater K, Westrum J, McDermott TR, Bothner B. Beyond Repression: ArsR Functions as a Global Activator of Metabolic and Redox Responses in Escherichia coli. Proteomes. 2026; 14(1):1. https://doi.org/10.3390/proteomes14010001
dc.identifier.doi10.3390/proteomes14010001
dc.identifier.issn2227-7382,
dc.identifier.urihttps://scholarworks.montana.edu/handle/1/19951
dc.language.isoen_US
dc.publisherMDPI AG
dc.rightscc-by
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.subjectArsR regulation
dc.subjectarsenic stress response
dc.subjectEscherichia coli proteome
dc.subjectArs operon expression
dc.subjectproteome stress response
dc.subjectdifferential proteome analysis
dc.subjectmass spectrometry-based proteomic analysis
dc.subjectproteomic pathway analysis
dc.titleBeyond Repression: ArsR Functions as a Global Activator of Metabolic and Redox Responses in Escherichia coli
dc.typeArticle
mus.citation.extentfirstpage1
mus.citation.extentlastpage20
mus.citation.issue1
mus.citation.journaltitleProteomes
mus.citation.volume14
mus.relation.collegeCollege of Letters & Science
mus.relation.collegeCollege of Agriculture
mus.relation.departmentChemistry & Biochemistry
mus.relation.departmentLand Resources & Environmental Sciences
mus.relation.universityMontana State University - Bozeman

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