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dc.contributor.authorGoksøyr, Siri Øfsthus
dc.contributor.authorGoldstone, Jed
dc.contributor.authorLille-Langøy, Roger
dc.contributor.authorLock, Erik Jan Robert
dc.contributor.authorOlsvik, Pål Asgeir
dc.contributor.authorGoksøyr, Anders
dc.contributor.authorKarlsen, Odd André
dc.date.accessioned2022-01-19T13:03:37Z
dc.date.available2022-01-19T13:03:37Z
dc.date.created2021-12-08T13:11:13Z
dc.date.issued2021
dc.identifier.citationAquatic Toxicology. 2021, 238 1-11.
dc.identifier.issn0166-445X
dc.identifier.urihttps://hdl.handle.net/11250/2838280
dc.description.abstractVitamin D receptor (VDR) mediates the biological function of the steroid hormone calcitriol, which is the metabolically active version of vitamin D. Calcitriol is important for a wide array of physiological functions, including calcium and phosphate homeostasis. In contrast to mammals, which harbor one VDR encoding gene, teleosts possess two orthologous vdr genes encoding Vdr alpha (Vdra) and Vdr beta (Vdrb). Genome mining identified the vdra and vdrb paralogs in the Atlantic cod (Gadus morhua) genome, which were further characterized regarding their phylogeny, tissue-specific expression, and transactivational properties induced by calcitriol. In addition, a selected set of polycyclic aromatic hydrocarbons (PAHs), including naphthalene, phenanthrene, fluorene, pyrene, chrysene, benzo[a]pyrene (BaP), and 7-methylbenzo[a]pyrene, were assessed for their ability to modulate the transcriptional activity of gmVdra and gmVdrb in vitro. Both gmVdra and gmVdrb were activated by calcitriol with similar potencies, but gmVdra produced significantly higher maximal fold activation. Notably, none of the tested PAHs showed agonistic properties towards the Atlantic cod Vdrs. However, binary exposures of calcitriol together with phenanthrene, fluorene, or pyrene, antagonized the activation of gmVdra, while chrysene and BaP significantly potentiated the calcitriol-mediated activity of both receptors. Homology modeling, solvent mapping, and docking analyses complemented the experimental data, and revealed a putative secondary binding site in addition to the canonical ligand-binding pocket (LBP). Calcitriol was predicted to interact with both binding sites, whereas PAHs docked primarily to the LBP. Importantly, our in vitro data suggest that PAHs can interact with the paralogous gmVdrs and interfere with their transcriptional activities, and thus potentially modulate the vitamin D signaling pathway and contribute to adverse effects of crude oil and PAH exposures on cardiac development and bone deformities in fish.
dc.language.isoeng
dc.titlePolycyclic aromatic hydrocarbons modulate the activity of Atlantic cod (Gadus morhua) vitamin D receptor paralogs in vitro
dc.typePeer reviewed
dc.typeJournal article
dc.description.versionpublishedVersion
dc.source.pagenumber1-11
dc.source.volume238
dc.source.journalAquatic Toxicology
dc.identifier.doi10.1016/j.aquatox.2021.105914
dc.identifier.cristin1966214
dc.relation.projectNorges forskningsråd: 248840
dc.relation.projectNorges forskningsråd: 244564
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode2


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