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

Onderstepoort Journal of Veterinary Research

 
 
Field Value
 
Title Development of real-time reverse transcription polymerase chain reaction assays to quantify insulin-like growth factor receptor and insulin receptor expression in equine tissue
 
Creator Hughes, Stephen B. Quan, Melvyn Guthrie, Alan Schulman, Martin
 
Subject Veterinary science: Molecular biology; Reproduction Equine; Insulin-like growth factor I; Insulin; Receptor; real-time RT-PCR; Development
Description The 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 insulin-like 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/µLand 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 insulin-like 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.
 
Publisher AOSIS
 
Contributor Department of Production Animal Studies Equine Research Centre —
Date 2013-08-30
 
Type info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion — Development
Format text/html application/octet-stream text/xml application/pdf
Identifier 10.4102/ojvr.v80i1.402
 
Source Onderstepoort Journal of Veterinary Research; Vol 80, No 1 (2013); 7 pages 2219-0635 0030-2465
 
Language eng
 
Relation
The following web links (URLs) may trigger a file download or direct you to an alternative webpage to gain access to a publication file format of the published article:

https://ojvr.org/index.php/ojvr/article/view/402/888 https://ojvr.org/index.php/ojvr/article/view/402/889 https://ojvr.org/index.php/ojvr/article/view/402/890 https://ojvr.org/index.php/ojvr/article/view/402/887
 
Coverage South Africa; Pretoria Current Equine
Rights Copyright (c) 2013 Stephen B. Hughes, Melvyn Quan, Alan Guthrie, Martin Schulman https://creativecommons.org/licenses/by-nd/4.0
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