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Ontogeny of hepatic metabolism in mule ducks highlights different gene expression profiles between carbohydrate and lipid metabolic pathways

BACKGROUND: The production of foie gras involves different metabolic pathways in the liver of overfed ducks such as lipid synthesis and carbohydrates catabolism, but the establishment of these pathways has not yet been described with precision during embryogenesis. The early environment can have sho...

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Autores principales: Massimino, William, Davail, Stéphane, Secula, Aurélie, Andrieux, Charlotte, Bernadet, Marie-Dominique, Pioche, Tracy, Ricaud, Karine, Gontier, Karine, Morisson, Mireille, Collin, Anne, Panserat, Stéphane, Houssier, Marianne
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7590481/
https://www.ncbi.nlm.nih.gov/pubmed/33109083
http://dx.doi.org/10.1186/s12864-020-07093-w
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author Massimino, William
Davail, Stéphane
Secula, Aurélie
Andrieux, Charlotte
Bernadet, Marie-Dominique
Pioche, Tracy
Ricaud, Karine
Gontier, Karine
Morisson, Mireille
Collin, Anne
Panserat, Stéphane
Houssier, Marianne
author_facet Massimino, William
Davail, Stéphane
Secula, Aurélie
Andrieux, Charlotte
Bernadet, Marie-Dominique
Pioche, Tracy
Ricaud, Karine
Gontier, Karine
Morisson, Mireille
Collin, Anne
Panserat, Stéphane
Houssier, Marianne
author_sort Massimino, William
collection PubMed
description BACKGROUND: The production of foie gras involves different metabolic pathways in the liver of overfed ducks such as lipid synthesis and carbohydrates catabolism, but the establishment of these pathways has not yet been described with precision during embryogenesis. The early environment can have short- and long-term impacts on the physiology of many animal species and can be used to influence physiological responses that is called programming. This study proposes to describe the basal hepatic metabolism at the level of mRNA in mule duck embryos in order to reveal potential interesting programming windows in the context of foie gras production. To this end, a kinetic study was designed to determine the level of expression of selected genes involved in steatosis-related liver functions throughout embryogenesis. The livers of 20 mule duck embryos were collected every 4 days from the 12th day of embryogenesis (E12) until 4 days after hatching (D4), and gene expression analysis was performed. The expression levels of 50 mRNAs were quantified for these 7 sampling points and classified into 4 major cellular pathways. RESULTS: Interestingly, most mRNAs involved in lipid metabolism are overexpressed after hatching (FASN, SCD1, ACOX1), whereas genes implicated in carbohydrate metabolism (HK1, GAPDH, GLUT1) and development (HGF, IGF, FGFR2) are predominantly overexpressed from E12 to E20. Finally, regarding cellular stress, gene expression appears quite stable throughout development, contrasting with strong expression after hatching (CYP2E1, HSBP1, HSP90AA1). CONCLUSION: For the first time we described the kinetics of hepatic ontogenesis at mRNA level in mule ducks and highlighted different expression patterns depending on the cellular pathway. These results could be particularly useful in the design of embryonic programming for the production of foie gras.
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spelling pubmed-75904812020-10-27 Ontogeny of hepatic metabolism in mule ducks highlights different gene expression profiles between carbohydrate and lipid metabolic pathways Massimino, William Davail, Stéphane Secula, Aurélie Andrieux, Charlotte Bernadet, Marie-Dominique Pioche, Tracy Ricaud, Karine Gontier, Karine Morisson, Mireille Collin, Anne Panserat, Stéphane Houssier, Marianne BMC Genomics Research Article BACKGROUND: The production of foie gras involves different metabolic pathways in the liver of overfed ducks such as lipid synthesis and carbohydrates catabolism, but the establishment of these pathways has not yet been described with precision during embryogenesis. The early environment can have short- and long-term impacts on the physiology of many animal species and can be used to influence physiological responses that is called programming. This study proposes to describe the basal hepatic metabolism at the level of mRNA in mule duck embryos in order to reveal potential interesting programming windows in the context of foie gras production. To this end, a kinetic study was designed to determine the level of expression of selected genes involved in steatosis-related liver functions throughout embryogenesis. The livers of 20 mule duck embryos were collected every 4 days from the 12th day of embryogenesis (E12) until 4 days after hatching (D4), and gene expression analysis was performed. The expression levels of 50 mRNAs were quantified for these 7 sampling points and classified into 4 major cellular pathways. RESULTS: Interestingly, most mRNAs involved in lipid metabolism are overexpressed after hatching (FASN, SCD1, ACOX1), whereas genes implicated in carbohydrate metabolism (HK1, GAPDH, GLUT1) and development (HGF, IGF, FGFR2) are predominantly overexpressed from E12 to E20. Finally, regarding cellular stress, gene expression appears quite stable throughout development, contrasting with strong expression after hatching (CYP2E1, HSBP1, HSP90AA1). CONCLUSION: For the first time we described the kinetics of hepatic ontogenesis at mRNA level in mule ducks and highlighted different expression patterns depending on the cellular pathway. These results could be particularly useful in the design of embryonic programming for the production of foie gras. BioMed Central 2020-10-27 /pmc/articles/PMC7590481/ /pubmed/33109083 http://dx.doi.org/10.1186/s12864-020-07093-w Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. 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 in a credit line to the data.
spellingShingle Research Article
Massimino, William
Davail, Stéphane
Secula, Aurélie
Andrieux, Charlotte
Bernadet, Marie-Dominique
Pioche, Tracy
Ricaud, Karine
Gontier, Karine
Morisson, Mireille
Collin, Anne
Panserat, Stéphane
Houssier, Marianne
Ontogeny of hepatic metabolism in mule ducks highlights different gene expression profiles between carbohydrate and lipid metabolic pathways
title Ontogeny of hepatic metabolism in mule ducks highlights different gene expression profiles between carbohydrate and lipid metabolic pathways
title_full Ontogeny of hepatic metabolism in mule ducks highlights different gene expression profiles between carbohydrate and lipid metabolic pathways
title_fullStr Ontogeny of hepatic metabolism in mule ducks highlights different gene expression profiles between carbohydrate and lipid metabolic pathways
title_full_unstemmed Ontogeny of hepatic metabolism in mule ducks highlights different gene expression profiles between carbohydrate and lipid metabolic pathways
title_short Ontogeny of hepatic metabolism in mule ducks highlights different gene expression profiles between carbohydrate and lipid metabolic pathways
title_sort ontogeny of hepatic metabolism in mule ducks highlights different gene expression profiles between carbohydrate and lipid metabolic pathways
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7590481/
https://www.ncbi.nlm.nih.gov/pubmed/33109083
http://dx.doi.org/10.1186/s12864-020-07093-w
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