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http://purl.uniprot.org/citations/33235221http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/33235221http://www.w3.org/2000/01/rdf-schema#comment"Hepatic lipogenesis is normally tightly regulated but is aberrantly elevated in obesity. Fibroblast Growth Factor-15/19 (mouse FGF15, human FGF19) are bile acid-induced late fed-state gut hormones that decrease hepatic lipid levels by unclear mechanisms. We show that FGF15/19 and FGF15/19-activated Small Heterodimer Partner (SHP/NR0B2) have a role in transcriptional repression of lipogenesis. Comparative genomic analyses reveal that most of the SHP cistrome, including lipogenic genes repressed by FGF19, have overlapping CpG islands. FGF19 treatment or SHP overexpression in mice inhibits lipogenesis in a DNA methyltransferase-3a (DNMT3A)-dependent manner. FGF19-mediated activation of SHP via phosphorylation recruits DNMT3A to lipogenic genes, leading to epigenetic repression via DNA methylation. In non-alcoholic fatty liver disease (NAFLD) patients and obese mice, occupancy of SHP and DNMT3A and DNA methylation at lipogenic genes are low, with elevated gene expression. In conclusion, FGF15/19 represses hepatic lipogenesis by activating SHP and DNMT3A physiologically, which is likely dysregulated in NAFLD."xsd:string
http://purl.uniprot.org/citations/33235221http://purl.org/dc/terms/identifier"doi:10.1038/s41467-020-19803-9"xsd:string
http://purl.uniprot.org/citations/33235221http://purl.uniprot.org/core/author"Ma J."xsd:string
http://purl.uniprot.org/citations/33235221http://purl.uniprot.org/core/author"Zhang Y."xsd:string
http://purl.uniprot.org/citations/33235221http://purl.uniprot.org/core/author"Kim Y.C."xsd:string
http://purl.uniprot.org/citations/33235221http://purl.uniprot.org/core/author"Guo G."xsd:string
http://purl.uniprot.org/citations/33235221http://purl.uniprot.org/core/author"Kemper B."xsd:string
http://purl.uniprot.org/citations/33235221http://purl.uniprot.org/core/author"Kemper J.K."xsd:string
http://purl.uniprot.org/citations/33235221http://purl.uniprot.org/core/author"Kong B."xsd:string
http://purl.uniprot.org/citations/33235221http://purl.uniprot.org/core/author"Seok S."xsd:string
http://purl.uniprot.org/citations/33235221http://purl.uniprot.org/core/date"2020"xsd:gYear
http://purl.uniprot.org/citations/33235221http://purl.uniprot.org/core/name"Nat Commun"xsd:string
http://purl.uniprot.org/citations/33235221http://purl.uniprot.org/core/pages"5969"xsd:string
http://purl.uniprot.org/citations/33235221http://purl.uniprot.org/core/title"Intestinal FGF15/19 physiologically repress hepatic lipogenesis in the late fed-state by activating SHP and DNMT3A."xsd:string
http://purl.uniprot.org/citations/33235221http://purl.uniprot.org/core/volume"11"xsd:string
http://purl.uniprot.org/citations/33235221http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/33235221
http://purl.uniprot.org/citations/33235221http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/33235221
http://purl.uniprot.org/uniprot/#_A0A140LIL5-mappedCitation-33235221http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/33235221
http://purl.uniprot.org/uniprot/#_Q62227-mappedCitation-33235221http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/33235221
http://purl.uniprot.org/uniprot/#_O35622-mappedCitation-33235221http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/33235221
http://purl.uniprot.org/uniprot/#_Q790L8-mappedCitation-33235221http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/33235221
http://purl.uniprot.org/uniprot/A0A140LIL5http://purl.uniprot.org/core/mappedCitationhttp://purl.uniprot.org/citations/33235221
http://purl.uniprot.org/uniprot/Q62227http://purl.uniprot.org/core/mappedCitationhttp://purl.uniprot.org/citations/33235221
http://purl.uniprot.org/uniprot/O35622http://purl.uniprot.org/core/mappedCitationhttp://purl.uniprot.org/citations/33235221