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Phylogenetic analysis and tissue distribution of elasmobranch glucose transporters and their response to feeding
Elasmobranch diets consist of high quantities of protein and lipids, but very low levels of carbohydrates including glucose. Reflecting this diet, most tissues use lipids and ketone bodies as their main metabolic fuel. However, the rectal gland has been shown to be dependent on glucose as a fuel, so...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Company of Biologists Ltd
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4810751/ https://www.ncbi.nlm.nih.gov/pubmed/26873951 http://dx.doi.org/10.1242/bio.016709 |
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author | Deck, Courtney A. LeMoine, Christophe M. R. Walsh, Patrick J. |
author_facet | Deck, Courtney A. LeMoine, Christophe M. R. Walsh, Patrick J. |
author_sort | Deck, Courtney A. |
collection | PubMed |
description | Elasmobranch diets consist of high quantities of protein and lipids, but very low levels of carbohydrates including glucose. Reflecting this diet, most tissues use lipids and ketone bodies as their main metabolic fuel. However, the rectal gland has been shown to be dependent on glucose as a fuel, so we hypothesized that glucose transporters (GLUTs) would be present and upregulated in the gland during times of activation (e.g. following a meal). In this study, we searched for and identified putative class I GLUTs in three elasmobranchs and a holocephalan using transcriptomes, and used these to reconstruct a Bayesian phylogeny. We determined that each of the four species possessed three of the four class I GLUT sequences, but the identities of the isoforms present in each species differed between the elasmobranchs (GLUT1, 3 and 4) and the holocephalan (GLUT1, 2 and 3). We then used qPCR to measure mRNA levels of these GLUTs in the rectal gland, liver, intestine, and muscle of fed and starved spiny dogfish (Squalus suckleyi). The rectal gland data showed higher mRNA levels of GLUT4 in the starved relative to the fed fish. In the muscle, both GLUT1 and 4 were significantly elevated at 24 h post-feeding, as was the case for GLUT4 in the liver. In the intestine on the other hand, GLUT4 was significantly elevated by 6 h post-feeding, remaining elevated through 48 h. We suggest that GLUT4 has taken on the role of GLUT2 in elasmobranchs as the expression patterns observed in the liver and intestine are representative of GLUT2 in other vertebrates. |
format | Online Article Text |
id | pubmed-4810751 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | The Company of Biologists Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-48107512016-04-04 Phylogenetic analysis and tissue distribution of elasmobranch glucose transporters and their response to feeding Deck, Courtney A. LeMoine, Christophe M. R. Walsh, Patrick J. Biol Open Research Article Elasmobranch diets consist of high quantities of protein and lipids, but very low levels of carbohydrates including glucose. Reflecting this diet, most tissues use lipids and ketone bodies as their main metabolic fuel. However, the rectal gland has been shown to be dependent on glucose as a fuel, so we hypothesized that glucose transporters (GLUTs) would be present and upregulated in the gland during times of activation (e.g. following a meal). In this study, we searched for and identified putative class I GLUTs in three elasmobranchs and a holocephalan using transcriptomes, and used these to reconstruct a Bayesian phylogeny. We determined that each of the four species possessed three of the four class I GLUT sequences, but the identities of the isoforms present in each species differed between the elasmobranchs (GLUT1, 3 and 4) and the holocephalan (GLUT1, 2 and 3). We then used qPCR to measure mRNA levels of these GLUTs in the rectal gland, liver, intestine, and muscle of fed and starved spiny dogfish (Squalus suckleyi). The rectal gland data showed higher mRNA levels of GLUT4 in the starved relative to the fed fish. In the muscle, both GLUT1 and 4 were significantly elevated at 24 h post-feeding, as was the case for GLUT4 in the liver. In the intestine on the other hand, GLUT4 was significantly elevated by 6 h post-feeding, remaining elevated through 48 h. We suggest that GLUT4 has taken on the role of GLUT2 in elasmobranchs as the expression patterns observed in the liver and intestine are representative of GLUT2 in other vertebrates. The Company of Biologists Ltd 2016-02-12 /pmc/articles/PMC4810751/ /pubmed/26873951 http://dx.doi.org/10.1242/bio.016709 Text en © 2016. Published by The Company of Biologists Ltd http://creativecommons.org/licenses/by/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0), which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed. |
spellingShingle | Research Article Deck, Courtney A. LeMoine, Christophe M. R. Walsh, Patrick J. Phylogenetic analysis and tissue distribution of elasmobranch glucose transporters and their response to feeding |
title | Phylogenetic analysis and tissue distribution of elasmobranch glucose transporters and their response to feeding |
title_full | Phylogenetic analysis and tissue distribution of elasmobranch glucose transporters and their response to feeding |
title_fullStr | Phylogenetic analysis and tissue distribution of elasmobranch glucose transporters and their response to feeding |
title_full_unstemmed | Phylogenetic analysis and tissue distribution of elasmobranch glucose transporters and their response to feeding |
title_short | Phylogenetic analysis and tissue distribution of elasmobranch glucose transporters and their response to feeding |
title_sort | phylogenetic analysis and tissue distribution of elasmobranch glucose transporters and their response to feeding |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4810751/ https://www.ncbi.nlm.nih.gov/pubmed/26873951 http://dx.doi.org/10.1242/bio.016709 |
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