Transcriptomic and metabolomic characterization of post-hatch metabolic reprogramming during hepatic development in the chicken

Abstract Background Artificial selection of modern meat-producing chickens (broilers) for production characteristics has led to dramatic changes in phenotype, yet the impact of this selection on metabolic and molecular mechanisms is poorly understood. The first 3 weeks post-hatch represent a critica...

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Main Authors: Heidi A. Van Every, Carl J. Schmidt
Format: Article
Language:English
Published: BMC 2021-05-01
Series:BMC Genomics
Subjects:
Online Access:https://doi.org/10.1186/s12864-021-07724-w
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spelling doaj-a034ada599da4dd89b13a93971d0a4d72021-05-30T11:25:47ZengBMCBMC Genomics1471-21642021-05-0122112110.1186/s12864-021-07724-wTranscriptomic and metabolomic characterization of post-hatch metabolic reprogramming during hepatic development in the chickenHeidi A. Van Every0Carl J. Schmidt1Center for Bioinformatics and Computational Biology, University of DelawareDepartment of Animal and Food Sciences, University of DelawareAbstract Background Artificial selection of modern meat-producing chickens (broilers) for production characteristics has led to dramatic changes in phenotype, yet the impact of this selection on metabolic and molecular mechanisms is poorly understood. The first 3 weeks post-hatch represent a critical period of adjustment, during which the yolk lipid is depleted and the bird transitions to reliance on a carbohydrate-rich diet. As the liver is the major organ involved in macronutrient metabolism and nutrient allocatytion, a combined transcriptomics and metabolomics approach has been used to evaluate hepatic metabolic reprogramming between Day 4 (D4) and Day 20 (D20) post-hatch. Results Many transcripts and metabolites involved in metabolic pathways differed in their abundance between D4 and D20, representing different stages of metabolism that are enhanced or diminished. For example, at D20 the first stage of glycolysis that utilizes ATP to store or release glucose is enhanced, while at D4, the ATP-generating phase is enhanced to provide energy for rapid cellular proliferation at this time point. This work has also identified several metabolites, including citrate, phosphoenolpyruvate, and glycerol, that appear to play pivotal roles in this reprogramming. Conclusions At Day 4, metabolic flexibility allows for efficiency to meet the demands of rapid liver growth under oxygen-limiting conditions. At Day 20, the liver’s metabolism has shifted to process a carbohydrate-rich diet that supports the rapid overall growth of the modern broiler. Characterizing these metabolic changes associated with normal post-hatch hepatic development has generated testable hypotheses about the involvement of specific genes and metabolites, clarified the importance of hypoxia to rapid organ growth, and contributed to our understanding of the molecular changes affected by decades of artificial selection.https://doi.org/10.1186/s12864-021-07724-wHigh-throughputCell proliferationMetabolic reprogrammingOrgan growthPathwayHypoxia
collection DOAJ
language English
format Article
sources DOAJ
author Heidi A. Van Every
Carl J. Schmidt
spellingShingle Heidi A. Van Every
Carl J. Schmidt
Transcriptomic and metabolomic characterization of post-hatch metabolic reprogramming during hepatic development in the chicken
BMC Genomics
High-throughput
Cell proliferation
Metabolic reprogramming
Organ growth
Pathway
Hypoxia
author_facet Heidi A. Van Every
Carl J. Schmidt
author_sort Heidi A. Van Every
title Transcriptomic and metabolomic characterization of post-hatch metabolic reprogramming during hepatic development in the chicken
title_short Transcriptomic and metabolomic characterization of post-hatch metabolic reprogramming during hepatic development in the chicken
title_full Transcriptomic and metabolomic characterization of post-hatch metabolic reprogramming during hepatic development in the chicken
title_fullStr Transcriptomic and metabolomic characterization of post-hatch metabolic reprogramming during hepatic development in the chicken
title_full_unstemmed Transcriptomic and metabolomic characterization of post-hatch metabolic reprogramming during hepatic development in the chicken
title_sort transcriptomic and metabolomic characterization of post-hatch metabolic reprogramming during hepatic development in the chicken
publisher BMC
series BMC Genomics
issn 1471-2164
publishDate 2021-05-01
description Abstract Background Artificial selection of modern meat-producing chickens (broilers) for production characteristics has led to dramatic changes in phenotype, yet the impact of this selection on metabolic and molecular mechanisms is poorly understood. The first 3 weeks post-hatch represent a critical period of adjustment, during which the yolk lipid is depleted and the bird transitions to reliance on a carbohydrate-rich diet. As the liver is the major organ involved in macronutrient metabolism and nutrient allocatytion, a combined transcriptomics and metabolomics approach has been used to evaluate hepatic metabolic reprogramming between Day 4 (D4) and Day 20 (D20) post-hatch. Results Many transcripts and metabolites involved in metabolic pathways differed in their abundance between D4 and D20, representing different stages of metabolism that are enhanced or diminished. For example, at D20 the first stage of glycolysis that utilizes ATP to store or release glucose is enhanced, while at D4, the ATP-generating phase is enhanced to provide energy for rapid cellular proliferation at this time point. This work has also identified several metabolites, including citrate, phosphoenolpyruvate, and glycerol, that appear to play pivotal roles in this reprogramming. Conclusions At Day 4, metabolic flexibility allows for efficiency to meet the demands of rapid liver growth under oxygen-limiting conditions. At Day 20, the liver’s metabolism has shifted to process a carbohydrate-rich diet that supports the rapid overall growth of the modern broiler. Characterizing these metabolic changes associated with normal post-hatch hepatic development has generated testable hypotheses about the involvement of specific genes and metabolites, clarified the importance of hypoxia to rapid organ growth, and contributed to our understanding of the molecular changes affected by decades of artificial selection.
topic High-throughput
Cell proliferation
Metabolic reprogramming
Organ growth
Pathway
Hypoxia
url https://doi.org/10.1186/s12864-021-07724-w
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