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dc.contributor.authorBrowning, Helen M.
dc.contributor.authorAcevedo-Whitehouse, Karina
dc.contributor.authorGulland, Frances M. D.
dc.contributor.authorHall, Ailsa J.
dc.contributor.authorFinlayson, Jeanie
dc.contributor.authorDagleish, Mark P.
dc.contributor.authorBillington, Karen J.
dc.contributor.authorColegrove, Kathleen
dc.contributor.authorHammond, John A.
dc.date.accessioned2014-11-17T15:31:02Z
dc.date.available2014-11-17T15:31:02Z
dc.date.issued2014-12
dc.identifier.citationBrowning , H M , Acevedo-Whitehouse , K , Gulland , F M D , Hall , A J , Finlayson , J , Dagleish , M P , Billington , K J , Colegrove , K & Hammond , J A 2014 , ' Evidence for a genetic basis of urogenital carcinoma in the wild California sea lion ' , Proceedings of the Royal Society B: Biological Sciences , vol. 281 , no. 1796 , 20140240 . https://doi.org/10.1098/rspb.2014.0240en
dc.identifier.issn0962-8452
dc.identifier.otherPURE: 155895591
dc.identifier.otherPURE UUID: 829a2dac-9971-40a3-a782-fd81ae880219
dc.identifier.otherRIS: urn:7333BE6A4110979558686F6C879EEC79
dc.identifier.otherScopus: 84908141398
dc.identifier.otherORCID: /0000-0002-7562-1771/work/47136273
dc.identifier.otherWOS: 000343674500001
dc.identifier.urihttps://hdl.handle.net/10023/5777
dc.descriptionThis work was funded by a grant from the US National Marine Fisheries Service John H. Prescott Marine Mammal Rescue Assistance grant programme, and H.M.B. was funded by a UK Natural Environment Research Council PhD studentship. J.A.H. was funded by the BBSRC Institute Strategic Programme on Livestock Viral Diseases at The Pirbright Institute.en
dc.description.abstractAlthough neoplasia is a major cause of mortality in humans and domestic animals, it has rarely been described in wildlife species. One of the fewexamples is a highly prevalent urogenital carcinoma in California sea lions (CSLs). Although the aetiology of this carcinoma is clearly multifactorial, inbreeding depression, as estimated using levels of microsatellite multilocus heterozygosity, is identified as predictive for this neoplasia. On further analysis, this relationship appears to be largely driven by one marker, suggesting that a single locus might be associated with the occurrence of this disease in CSLs. In a case–control study, carcinoma was significantly associated with homozygosity at the Pv11 microsatellite locus. Pv11 was mapped to intron 9 of the heparanase 2 gene (HPSE2) locus, a very large gene encoding heparanase 2, which in humans is associated with multiple carcinomas. Correspondingly, immunohistochemical labelling in tissues was present in carcinoma cases within a single homozygous Pv11 genotype. To our knowledge, this is the first report of an individual locus being associated with cancer in any wildlife species. This adds emphasis to the study of HPSE2 in other species, including humans and will guide future studies on this sentinel species that shares much of its diet and environment with humans
dc.format.extent10
dc.language.isoeng
dc.relation.ispartofProceedings of the Royal Society B: Biological Sciencesen
dc.rights© 2014. The Authors. Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/, which permits unrestricted use, provided the original author and source are credited.en
dc.subjectCanceren
dc.subjectHeparanase 2 geneen
dc.subjectWildlifeen
dc.subjectOdds ratioen
dc.subjectQH301 Biologyen
dc.subjectSDG 3 - Good Health and Well-beingen
dc.subject.lccQH301en
dc.titleEvidence for a genetic basis of urogenital carcinoma in the wild California sea lionen
dc.typeJournal articleen
dc.contributor.sponsorNERCen
dc.description.versionPublisher PDFen
dc.contributor.institutionUniversity of St Andrews. School of Biologyen
dc.contributor.institutionUniversity of St Andrews. Sea Mammal Research Uniten
dc.contributor.institutionUniversity of St Andrews. Marine Alliance for Science & Technology Scotlanden
dc.contributor.institutionUniversity of St Andrews. Scottish Oceans Instituteen
dc.identifier.doihttps://doi.org/10.1098/rspb.2014.0240
dc.description.statusPeer revieweden
dc.identifier.urlhttp://rspb.royalsocietypublishing.org/content/281/1796/20140240.en
dc.identifier.grantnumberAgreement R8-H12-86en


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