Development of real-time reverse transcription polymerase chain reaction assays to quantify insulin-like growth factor receptor and insulin receptor expression in equine tissue

dc.contributor.authorHughes, Stephen Bernard
dc.contributor.authorQuan, Melvyn
dc.contributor.authorGuthrie, Alan John
dc.contributor.authorSchulman, M.L. (Martin)
dc.date.accessioned2014-07-01T12:14:05Z
dc.date.available2014-07-01T12:14:05Z
dc.date.issued2013-08-30
dc.description.abstractThe insulin-like growth factor system (insulin-like growth factor 1, insulin-like growth factor 2, insulin-like growth factor 1 receptor, insulin-like growth factor 2 receptor and six insulinlike growth factor-binding proteins) and insulin are essential to muscle metabolism and most aspects of male and female reproduction. Insulin-like growth factor and insulin play important roles in the regulation of cell growth, differentiation and the maintenance of cell differentiation in mammals. In order to better understand the local factors that regulate equine physiology, such as muscle metabolism and reproduction (e.g., germ cell development and fertilisation), real-time reverse transcription polymerase chain reaction assays for quantification of equine insulin-like growth factor 1 receptor and insulin receptor messenger ribonucleic acid were developed. The assays were sensitive: 192 copies/μL and 891 copies/μL for insulin-like growth factor 1 receptor, messenger ribonucleic acid and insulin receptor respectively (95% limit of detection), and efficient: 1.01 for the insulin-like growth factor 1 receptor assay and 0.95 for the insulin receptor assay. The assays had a broad linear range of detection (seven logs for insulinlike growth factor 1 receptor and six logs for insulin receptor). This allowed for analysis of very small amounts of messenger ribonucleic acid. Low concentrations of both insulin-like growth factor 1 receptor and insulin receptor messenger ribonucleic acid were detected in endometrium, lung and spleen samples, whilst high concentrations were detected in heart, muscle and kidney samples, this was most likely due to the high level of glucose metabolism and glucose utilisation by these tissues. The assays developed for insulin-like growth factor 1 receptor and insulin receptor messenger ribonucleic acid expression have been shown to work on equine tissue and will contribute to the understanding of insulin and insulin-like growth factor 1 receptor physiology in the horse.en_US
dc.description.librarianam2014en_US
dc.description.urihttp://www.ojvr.orgen_US
dc.identifier.citationStephen B., Hughes, S.B., Quan, M., Guthrie, A. & Schulman, M., 2013, ‘Development of realtime reverse transcription polymerase chain reaction assays to quantify insulin-like growth factor and insulin receptor expression in equine tissue’, Onderstepoort Journal of Veterinary Research 80(1), Art. #402, 7 pages. http://dx.DOI.org/ 10.4102/ojvr.v80i1.402en_US
dc.identifier.issn0030-2465 (print)
dc.identifier.issn2219-0635 (online)
dc.identifier.other10.4102/ojvr.v80i1.402
dc.identifier.other24338988000
dc.identifier.otherN-9316-2014
dc.identifier.other0000-0003-3352-8488
dc.identifier.other7006535470
dc.identifier.otherJ-6375-2013
dc.identifier.other0000-0001-7729-9918
dc.identifier.urihttp://hdl.handle.net/2263/40480
dc.language.isoenen_US
dc.publisherAOSIS Open Journalsen_US
dc.relation.requiresAdobe Acrobat Readeren
dc.rights© 2013. The Authors. Licensee: AOSIS OpenJournals. This work is licensed under the Creative Commons Attribution License.en_US
dc.subjectEquine tissueen_US
dc.subjectInsulin-like growth factor receptoren_US
dc.subjectInsulin receptor expressionen_US
dc.subjectGene expression analysisen_US
dc.subjectPolymerase chain reaction assaysen_US
dc.titleDevelopment of real-time reverse transcription polymerase chain reaction assays to quantify insulin-like growth factor receptor and insulin receptor expression in equine tissueen_US
dc.typeArticleen_US

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