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http://purl.uniprot.org/citations/34972106http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/34972106http://www.w3.org/2000/01/rdf-schema#comment"Relaxin/insulin-like family peptide receptor 1 (RXFP1) mediates relaxin's antifibrotic effects and has reduced expression in the lung and skin of patients with fibrotic interstitial lung disease (fILD) including idiopathic pulmonary fibrosis (IPF) and systemic sclerosis (SSc). This may explain the failure of relaxin-based anti-fibrotic treatments in SSc, but the regulatory mechanisms controlling RXFP1 expression remain largely unknown. This study aimed to identify regulatory elements of RXFP1 that may function differentially in fibrotic fibroblasts. We identified and evaluated a distal regulatory region of RXFP1 in lung fibroblasts using a luciferase reporter system. Using serial deletions, an enhancer upregulating pGL3-promoter activity was localized to the distal region between -584 to -242bp from the distal transcription start site (TSS). This enhancer exhibited reduced activity in IPF and SSc lung fibroblasts. Bioinformatic analysis identified two clusters of activator protein 1 (AP-1) transcription factor binding sites within the enhancer. Site-directed mutagenesis of the binding sites confirmed that only one cluster reduced activity (-358 to -353 relative to distal TSS). Co-expression of FOS in lung fibroblasts further increased enhancer activity. In vitro complex formation with a labeled probe spanning the functional AP-1 site using nuclear proteins isolated from lung fibroblasts confirmed a specific DNA/protein complex formation. Application of antibodies against JUN and FOS resulted in the complex alteration, while antibodies to JUNB and FOSL1 did not. Analysis of AP-1 binding in 5 pairs of control and IPF lung fibroblasts detected positive binding more frequently in control fibroblasts. Expression of JUN and FOS was reduced and correlated positively with RXFP1 expression in IPF lungs. In conclusion, we identified a distal enhancer of RXFP1 with differential activity in fibrotic lung fibroblasts involving AP-1 transcription factors. Our study provides insight into RXFP1 downregulation in fILD and may support efforts to reevaluate relaxin-based therapeutics alongside upregulation of RXFP1 transcription."xsd:string
http://purl.uniprot.org/citations/34972106http://purl.org/dc/terms/identifier"doi:10.1371/journal.pone.0254466"xsd:string
http://purl.uniprot.org/citations/34972106http://purl.uniprot.org/core/author"Li X."xsd:string
http://purl.uniprot.org/citations/34972106http://purl.uniprot.org/core/author"Tan J."xsd:string
http://purl.uniprot.org/citations/34972106http://purl.uniprot.org/core/author"Zhang Y."xsd:string
http://purl.uniprot.org/citations/34972106http://purl.uniprot.org/core/author"Hung C.H."xsd:string
http://purl.uniprot.org/citations/34972106http://purl.uniprot.org/core/author"Hamilton K."xsd:string
http://purl.uniprot.org/citations/34972106http://purl.uniprot.org/core/author"Chen T.Y."xsd:string
http://purl.uniprot.org/citations/34972106http://purl.uniprot.org/core/author"Bahudhanapati H."xsd:string
http://purl.uniprot.org/citations/34972106http://purl.uniprot.org/core/author"Kass D.J."xsd:string
http://purl.uniprot.org/citations/34972106http://purl.uniprot.org/core/author"Goobie G.C."xsd:string
http://purl.uniprot.org/citations/34972106http://purl.uniprot.org/core/author"Hung T.K."xsd:string
http://purl.uniprot.org/citations/34972106http://purl.uniprot.org/core/date"2021"xsd:gYear
http://purl.uniprot.org/citations/34972106http://purl.uniprot.org/core/name"PLoS One"xsd:string
http://purl.uniprot.org/citations/34972106http://purl.uniprot.org/core/pages"e0254466"xsd:string
http://purl.uniprot.org/citations/34972106http://purl.uniprot.org/core/title"Identification of a distal RXFP1 gene enhancer with differential activity in fibrotic lung fibroblasts involving AP-1."xsd:string
http://purl.uniprot.org/citations/34972106http://purl.uniprot.org/core/volume"16"xsd:string
http://purl.uniprot.org/citations/34972106http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/34972106
http://purl.uniprot.org/citations/34972106http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/34972106
http://purl.uniprot.org/uniprot/#_A0A0A0MT52-mappedCitation-34972106http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/34972106
http://purl.uniprot.org/uniprot/#_A0A087WWV0-mappedCitation-34972106http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/34972106
http://purl.uniprot.org/uniprot/#_A0A510GAI3-mappedCitation-34972106http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/34972106
http://purl.uniprot.org/uniprot/#_B3KV27-mappedCitation-34972106http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/34972106
http://purl.uniprot.org/uniprot/#_B4DGP2-mappedCitation-34972106http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/34972106