Transcriptional characterization of porcine leptin and leptin receptor genes

The leptin (LEP) and its receptor (LEPR) regulate food intake and energy balance through hypothalamic signaling. However, the LEP-LEPR axis seems to be more complex and its expression regulation has not been well described. In pigs, LEP and LEPR genes have been widely studied due to their relevance. Previous studies reported significant effects of SNPs located in both genes on growth and fatness traits. The aim of this study was to determine the expression profiles of LEP and LEPR across hypothalamic, adipose, hepatic and muscle tissues in Iberian x Landrace backcrossed pigs and to analyze the effects of gene variants on transcript abundance. To our knowledge, non porcine LEPR isoforms have been described rather than LEPRb. A short porcine LEPR isoform (LEPRa), that encodes a protein lacking the intracellular residues responsible of signal transduction, has been identified for the first time. The LEPRb isoform was only quantifiable in hypothalamus while LEPRa appeared widely expressed across tissues, but at higher levels in liver, suggesting that both isoforms would develop different roles. The unique LEP transcript showed expression in backfat and muscle. The effects of gene variants on transcript expression revealed interesting results. The LEPRc.1987C>T polymorphism showed opposite effects on LEPRb and LEPRa hypothalamic expression. In addition, one out of the 16 polymorphisms identified in the LEPR promoter region revealed high differential expression in hepatic LEPRa. These results suggest a LEPR isoform-specific regulation at tissue level. Conversely, non-differential expression of LEP conditional on the analyzed polymorphisms could be detected, indicating that its regulation is likely affected by other mechanisms rather than gene sequence variants. The present study has allowed a transcriptional characterization of LEP and LEPR isoforms on a range of tissues. Their expression patterns seem to indicate that both molecules develop peripheral roles apart from their known hypothalamic signal transduction function. © 2013 Pérez-Montarelo et al.

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Main Authors: Pérez-Montarelo, D., Fernández, A., Barragán, C., Noguera, J. L., Folch, J. M., Rodríguez, M. C., Óvilo, C., Silió, L., Fernández, A. I.
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Language:eng
Published: 2013
Online Access:http://hdl.handle.net/20.500.12792/3467
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spelling dig-inia-es-20.500.12792-34672020-12-15T09:46:42Z Transcriptional characterization of porcine leptin and leptin receptor genes Pérez-Montarelo, D. Fernández, A. Barragán, C. Noguera, J. L. Folch, J. M. Rodríguez, M. C. Óvilo, C. Silió, L. Fernández, A. I. The leptin (LEP) and its receptor (LEPR) regulate food intake and energy balance through hypothalamic signaling. However, the LEP-LEPR axis seems to be more complex and its expression regulation has not been well described. In pigs, LEP and LEPR genes have been widely studied due to their relevance. Previous studies reported significant effects of SNPs located in both genes on growth and fatness traits. The aim of this study was to determine the expression profiles of LEP and LEPR across hypothalamic, adipose, hepatic and muscle tissues in Iberian x Landrace backcrossed pigs and to analyze the effects of gene variants on transcript abundance. To our knowledge, non porcine LEPR isoforms have been described rather than LEPRb. A short porcine LEPR isoform (LEPRa), that encodes a protein lacking the intracellular residues responsible of signal transduction, has been identified for the first time. The LEPRb isoform was only quantifiable in hypothalamus while LEPRa appeared widely expressed across tissues, but at higher levels in liver, suggesting that both isoforms would develop different roles. The unique LEP transcript showed expression in backfat and muscle. The effects of gene variants on transcript expression revealed interesting results. The LEPRc.1987C>T polymorphism showed opposite effects on LEPRb and LEPRa hypothalamic expression. In addition, one out of the 16 polymorphisms identified in the LEPR promoter region revealed high differential expression in hepatic LEPRa. These results suggest a LEPR isoform-specific regulation at tissue level. Conversely, non-differential expression of LEP conditional on the analyzed polymorphisms could be detected, indicating that its regulation is likely affected by other mechanisms rather than gene sequence variants. The present study has allowed a transcriptional characterization of LEP and LEPR isoforms on a range of tissues. Their expression patterns seem to indicate that both molecules develop peripheral roles apart from their known hypothalamic signal transduction function. © 2013 Pérez-Montarelo et al. 2020-10-22T14:44:33Z 2020-10-22T14:44:33Z 2013 journal article http://hdl.handle.net/20.500.12792/3467 10.1371/journal.pone.0066398 eng Attribution-NonCommercial-ShareAlike 4.0 International http://creativecommons.org/licenses/by-nc-sa/4.0/ open access
institution INIA ES
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country España
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language eng
description The leptin (LEP) and its receptor (LEPR) regulate food intake and energy balance through hypothalamic signaling. However, the LEP-LEPR axis seems to be more complex and its expression regulation has not been well described. In pigs, LEP and LEPR genes have been widely studied due to their relevance. Previous studies reported significant effects of SNPs located in both genes on growth and fatness traits. The aim of this study was to determine the expression profiles of LEP and LEPR across hypothalamic, adipose, hepatic and muscle tissues in Iberian x Landrace backcrossed pigs and to analyze the effects of gene variants on transcript abundance. To our knowledge, non porcine LEPR isoforms have been described rather than LEPRb. A short porcine LEPR isoform (LEPRa), that encodes a protein lacking the intracellular residues responsible of signal transduction, has been identified for the first time. The LEPRb isoform was only quantifiable in hypothalamus while LEPRa appeared widely expressed across tissues, but at higher levels in liver, suggesting that both isoforms would develop different roles. The unique LEP transcript showed expression in backfat and muscle. The effects of gene variants on transcript expression revealed interesting results. The LEPRc.1987C>T polymorphism showed opposite effects on LEPRb and LEPRa hypothalamic expression. In addition, one out of the 16 polymorphisms identified in the LEPR promoter region revealed high differential expression in hepatic LEPRa. These results suggest a LEPR isoform-specific regulation at tissue level. Conversely, non-differential expression of LEP conditional on the analyzed polymorphisms could be detected, indicating that its regulation is likely affected by other mechanisms rather than gene sequence variants. The present study has allowed a transcriptional characterization of LEP and LEPR isoforms on a range of tissues. Their expression patterns seem to indicate that both molecules develop peripheral roles apart from their known hypothalamic signal transduction function. © 2013 Pérez-Montarelo et al.
format journal article
author Pérez-Montarelo, D.
Fernández, A.
Barragán, C.
Noguera, J. L.
Folch, J. M.
Rodríguez, M. C.
Óvilo, C.
Silió, L.
Fernández, A. I.
spellingShingle Pérez-Montarelo, D.
Fernández, A.
Barragán, C.
Noguera, J. L.
Folch, J. M.
Rodríguez, M. C.
Óvilo, C.
Silió, L.
Fernández, A. I.
Transcriptional characterization of porcine leptin and leptin receptor genes
author_facet Pérez-Montarelo, D.
Fernández, A.
Barragán, C.
Noguera, J. L.
Folch, J. M.
Rodríguez, M. C.
Óvilo, C.
Silió, L.
Fernández, A. I.
author_sort Pérez-Montarelo, D.
title Transcriptional characterization of porcine leptin and leptin receptor genes
title_short Transcriptional characterization of porcine leptin and leptin receptor genes
title_full Transcriptional characterization of porcine leptin and leptin receptor genes
title_fullStr Transcriptional characterization of porcine leptin and leptin receptor genes
title_full_unstemmed Transcriptional characterization of porcine leptin and leptin receptor genes
title_sort transcriptional characterization of porcine leptin and leptin receptor genes
publishDate 2013
url http://hdl.handle.net/20.500.12792/3467
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