PTPN2 copper-sensing relays copper level fluctuations into EGFR/CREB activation and associated CTR1 transcriptional repression
Year: 2024
Type: article
Abstract: Fluxes in human copper levels recently garnered attention for roles in cellular signaling, including affecting levels of the signaling molecule cyclic adenosine monophosphate. We herein apply an unbiased temporal evaluation of the signaling and whole genome transcriptional activities modulated by copper level fluctuations to identify potential copper sensor proteins responsible for driving these activities. We find that fluctuations in physiologically relevant copper levels modulate EGFR signal transduction and activation of the transcription factor CREB. Both intracellular and extracellular assays support Cu 1+ inhibition of the EGFR phosphatase PTPN2 (and potentially PTPN1)–via ligation to the PTPN2 active site cysteine side chain–as the underlying mechanism. We additionally show i ) copper supplementation drives weak transcriptional repression of the copper importer CTR1 and ii ) CREB activity is inversely correlated with CTR1 expression. In summary, our study reveals PTPN2 as a physiological copper sensor and defines a regulatory mechanism linking feedback control of copper stimulated EGFR/CREB signaling and CTR1 expression.
Source: Nature Communications
Institutions: University of Chicago, Howard Hughes Medical Institute
Language: English
Topic: Trace Elements in Health
Subfield: Nutrition and Dietetics
Field: Nursing
Domain: Health Sciences
Open Access status: gold
Estimated APC paid: $6,790
Awards: G1477498699, G1624506298, G2016810534, G3560837801, G4722685567, Heavy metal-stimulated signal transduction: new metal-regulatory and -responsive mechanisms, G62933622, G9000007279, G9000069798, Structural and Functional Studies of Molecular Machines Involved in Chemical Modifications of Macromolecules, Labeling and sequencing of 5hmC and 5mC in DNA-Renewal, Direct Oxidative Nucleic Acids Demethylation, G955445736
OpenAlex ID: W4401536444
