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Cloning and tissue distribution of novel splice variants of the ovine ghrelin gene
BACKGROUND: The ghrelin axis is involved in the regulation of metabolism, energy balance, and the immune, cardiovascular and reproductive systems. The manipulation of this axis has potential for improving economically valuable traits in production animals, and polymorphisms in the ghrelin (GHRL) and...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4172912/ https://www.ncbi.nlm.nih.gov/pubmed/25350131 http://dx.doi.org/10.1186/s12917-014-0211-x |
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author | Menzies, Moira Seim, Inge Josh, Peter Nagaraj, Shivashankar H Lees, Michael Walpole, Carina Chopin, Lisa K Colgrave, Michelle Ingham, Aaron |
author_facet | Menzies, Moira Seim, Inge Josh, Peter Nagaraj, Shivashankar H Lees, Michael Walpole, Carina Chopin, Lisa K Colgrave, Michelle Ingham, Aaron |
author_sort | Menzies, Moira |
collection | PubMed |
description | BACKGROUND: The ghrelin axis is involved in the regulation of metabolism, energy balance, and the immune, cardiovascular and reproductive systems. The manipulation of this axis has potential for improving economically valuable traits in production animals, and polymorphisms in the ghrelin (GHRL) and ghrelin receptor (GHSR) genes have been associated with growth and carcass traits. Here we investigate the structure and expression of the ghrelin gene (GHRL) in sheep, Ovis aries. RESULTS: We identify two ghrelin mRNA isoforms, which we have designated Δex2 preproghrelin and Δex2,3 preproghrelin. Expression of Δex2,3 preproghrelin is likely to be restricted to ruminants, and would encode truncated ghrelin and a novel C-terminal peptide. Both Δex2 preproghrelin and canonical preproghrelin mRNA isoforms were expressed in a range of tissues. Expression of the Δex2,3 preproghrelin isoform, however, was restricted to white blood cells (WBC; where the wild-type preproghrelin isoform is not co-expressed), and gastrointestinal tissues. Expression of Δex2 preproghrelin and Δex2,3 preproghrelin mRNA was elevated in white blood cells in response to parasitic worm (helminth) infection in genetically susceptible sheep, but not in resistant sheep. CONCLUSIONS: The restricted expression of the novel preproghrelin variants and their distinct WBC expression pattern during parasite infection may indicate a novel link between the ghrelin axis and metabolic and immune function in ruminants. |
format | Online Article Text |
id | pubmed-4172912 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-41729122014-09-25 Cloning and tissue distribution of novel splice variants of the ovine ghrelin gene Menzies, Moira Seim, Inge Josh, Peter Nagaraj, Shivashankar H Lees, Michael Walpole, Carina Chopin, Lisa K Colgrave, Michelle Ingham, Aaron BMC Vet Res Research Article BACKGROUND: The ghrelin axis is involved in the regulation of metabolism, energy balance, and the immune, cardiovascular and reproductive systems. The manipulation of this axis has potential for improving economically valuable traits in production animals, and polymorphisms in the ghrelin (GHRL) and ghrelin receptor (GHSR) genes have been associated with growth and carcass traits. Here we investigate the structure and expression of the ghrelin gene (GHRL) in sheep, Ovis aries. RESULTS: We identify two ghrelin mRNA isoforms, which we have designated Δex2 preproghrelin and Δex2,3 preproghrelin. Expression of Δex2,3 preproghrelin is likely to be restricted to ruminants, and would encode truncated ghrelin and a novel C-terminal peptide. Both Δex2 preproghrelin and canonical preproghrelin mRNA isoforms were expressed in a range of tissues. Expression of the Δex2,3 preproghrelin isoform, however, was restricted to white blood cells (WBC; where the wild-type preproghrelin isoform is not co-expressed), and gastrointestinal tissues. Expression of Δex2 preproghrelin and Δex2,3 preproghrelin mRNA was elevated in white blood cells in response to parasitic worm (helminth) infection in genetically susceptible sheep, but not in resistant sheep. CONCLUSIONS: The restricted expression of the novel preproghrelin variants and their distinct WBC expression pattern during parasite infection may indicate a novel link between the ghrelin axis and metabolic and immune function in ruminants. BioMed Central 2014-09-06 /pmc/articles/PMC4172912/ /pubmed/25350131 http://dx.doi.org/10.1186/s12917-014-0211-x Text en © Menzies et al.; licensee BioMed Central Ltd. 2014 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Menzies, Moira Seim, Inge Josh, Peter Nagaraj, Shivashankar H Lees, Michael Walpole, Carina Chopin, Lisa K Colgrave, Michelle Ingham, Aaron Cloning and tissue distribution of novel splice variants of the ovine ghrelin gene |
title | Cloning and tissue distribution of novel splice variants of the ovine ghrelin gene |
title_full | Cloning and tissue distribution of novel splice variants of the ovine ghrelin gene |
title_fullStr | Cloning and tissue distribution of novel splice variants of the ovine ghrelin gene |
title_full_unstemmed | Cloning and tissue distribution of novel splice variants of the ovine ghrelin gene |
title_short | Cloning and tissue distribution of novel splice variants of the ovine ghrelin gene |
title_sort | cloning and tissue distribution of novel splice variants of the ovine ghrelin gene |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4172912/ https://www.ncbi.nlm.nih.gov/pubmed/25350131 http://dx.doi.org/10.1186/s12917-014-0211-x |
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