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


Journal

BMC genomics
ISSN: 1471-2164
Titre abrégé: BMC Genomics
Pays: England
ID NLM: 100965258

Informations de publication

Date de publication:
27 Oct 2020
Historique:
received: 05 03 2020
accepted: 22 09 2020
entrez: 28 10 2020
pubmed: 29 10 2020
medline: 15 5 2021
Statut: epublish

Résumé

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. 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). 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.

Sections du résumé

BACKGROUND 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 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 CONCLUSIONS
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.

Identifiants

pubmed: 33109083
doi: 10.1186/s12864-020-07093-w
pii: 10.1186/s12864-020-07093-w
pmc: PMC7590481
doi:

Substances chimiques

Carbohydrates 0
Lipids 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

742

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Auteurs

William Massimino (W)

Univ Pau & Pays Adour, INRAE, E2S UPPA, UMR 1419, Nutrition, Métabolisme, Aquaculture, F-64310, Saint Pée sur Nivelle, France.

Stéphane Davail (S)

Univ Pau & Pays Adour, INRAE, E2S UPPA, UMR 1419, Nutrition, Métabolisme, Aquaculture, F-64310, Saint Pée sur Nivelle, France.

Aurélie Secula (A)

IHAP, Université de Toulouse, ENVT, INRAE, UMR 1225, 31076, Toulouse, France.

Charlotte Andrieux (C)

Univ Pau & Pays Adour, INRAE, E2S UPPA, UMR 1419, Nutrition, Métabolisme, Aquaculture, F-64310, Saint Pée sur Nivelle, France.

Marie-Dominique Bernadet (MD)

INRAE Bordeaux-Aquitaine, UEPFG (Unité Expérimentale Palmipèdes à Foie Gras), Domaine d'Artiguères 1076, route de Haut Mauco, F-40280, Benquet, France.

Tracy Pioche (T)

Univ Pau & Pays Adour, INRAE, E2S UPPA, UMR 1419, Nutrition, Métabolisme, Aquaculture, F-64310, Saint Pée sur Nivelle, France.

Karine Ricaud (K)

Univ Pau & Pays Adour, INRAE, E2S UPPA, UMR 1419, Nutrition, Métabolisme, Aquaculture, F-64310, Saint Pée sur Nivelle, France.

Karine Gontier (K)

Univ Pau & Pays Adour, INRAE, E2S UPPA, UMR 1419, Nutrition, Métabolisme, Aquaculture, F-64310, Saint Pée sur Nivelle, France.

Mireille Morisson (M)

GenPhySE, Université de Toulouse, INRAE, ENVT, F-31326, Castanet Tolosan, France.

Anne Collin (A)

INRAE, Université de Tours, BOA, 37380, Nouzilly, France.

Stéphane Panserat (S)

Univ Pau & Pays Adour, INRAE, E2S UPPA, UMR 1419, Nutrition, Métabolisme, Aquaculture, F-64310, Saint Pée sur Nivelle, France.

Marianne Houssier (M)

Univ Pau & Pays Adour, INRAE, E2S UPPA, UMR 1419, Nutrition, Métabolisme, Aquaculture, F-64310, Saint Pée sur Nivelle, France. marianne.houssier@univ-pau.fr.

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Classifications MeSH