Cargando…

Transcriptional profiling of liver during the critical embryo-to-hatchling transition period in the chicken (Gallus gallus)

BACKGROUND: Although hatching is perhaps the most abrupt and profound metabolic challenge that a chicken must undergo; there have been no attempts to functionally map the metabolic pathways induced in liver during the embryo-to-hatchling transition. Furthermore, we know very little about the metabol...

Descripción completa

Detalles Bibliográficos
Autores principales: Cogburn, Larry A., Trakooljul, Nares, Chen, Chuming, Huang, Hongzhan, Wu, Cathy H., Carré, Wilfrid, Wang, Xiaofei, White, Harold B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6151027/
https://www.ncbi.nlm.nih.gov/pubmed/30241500
http://dx.doi.org/10.1186/s12864-018-5080-4
_version_ 1783357088823508992
author Cogburn, Larry A.
Trakooljul, Nares
Chen, Chuming
Huang, Hongzhan
Wu, Cathy H.
Carré, Wilfrid
Wang, Xiaofei
White, Harold B.
author_facet Cogburn, Larry A.
Trakooljul, Nares
Chen, Chuming
Huang, Hongzhan
Wu, Cathy H.
Carré, Wilfrid
Wang, Xiaofei
White, Harold B.
author_sort Cogburn, Larry A.
collection PubMed
description BACKGROUND: Although hatching is perhaps the most abrupt and profound metabolic challenge that a chicken must undergo; there have been no attempts to functionally map the metabolic pathways induced in liver during the embryo-to-hatchling transition. Furthermore, we know very little about the metabolic and regulatory factors that regulate lipid metabolism in late embryos or newly-hatched chicks. In the present study, we examined hepatic transcriptomes of 12 embryos and 12 hatchling chicks during the peri-hatch period—or the metabolic switch from chorioallantoic to pulmonary respiration. RESULTS: Initial hierarchical clustering revealed two distinct, albeit opposing, patterns of hepatic gene expression. Cluster A genes are largely lipolytic and highly expressed in embryos. While, Cluster B genes are lipogenic/thermogenic and mainly controlled by the lipogenic transcription factor THRSPA. Using pairwise comparisons of embryo and hatchling ages, we found 1272 genes that were differentially expressed between embryos and hatchling chicks, including 24 transcription factors and 284 genes that regulate lipid metabolism. The three most differentially-expressed transcripts found in liver of embryos were MOGAT1, DIO3 and PDK4, whereas THRSPA, FASN and DIO2 were highest in hatchlings. An unusual finding was the “ectopic” and extremely high differentially expression of seven feather keratin transcripts in liver of 16 day embryos, which coincides with engorgement of liver with yolk lipids. Gene interaction networks show several transcription factors, transcriptional co-activators/co-inhibitors and their downstream genes that exert a ‘ying-yang’ action on lipid metabolism during the embryo-to-hatching transition. These upstream regulators include ligand-activated transcription factors, sirtuins and Kruppel-like factors. CONCLUSIONS: Our genome-wide transcriptional analysis has greatly expanded the hepatic repertoire of regulatory and metabolic genes involved in the embryo-to-hatchling transition. New knowledge was gained on interactive transcriptional networks and metabolic pathways that enable the abrupt switch from ectothermy (embryo) to endothermy (hatchling) in the chicken. Several transcription factors and their coactivators/co-inhibitors appear to exert opposing actions on lipid metabolism, leading to the predominance of lipolysis in embryos and lipogenesis in hatchlings. Our analysis of hepatic transcriptomes has enabled discovery of opposing, interconnected and interdependent transcriptional regulators that provide precise ying-yang or homeorhetic regulation of lipid metabolism during the critical embryo-to-hatchling transition. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12864-018-5080-4) contains supplementary material, which is available to authorized users.
format Online
Article
Text
id pubmed-6151027
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-61510272018-09-26 Transcriptional profiling of liver during the critical embryo-to-hatchling transition period in the chicken (Gallus gallus) Cogburn, Larry A. Trakooljul, Nares Chen, Chuming Huang, Hongzhan Wu, Cathy H. Carré, Wilfrid Wang, Xiaofei White, Harold B. BMC Genomics Research Article BACKGROUND: Although hatching is perhaps the most abrupt and profound metabolic challenge that a chicken must undergo; there have been no attempts to functionally map the metabolic pathways induced in liver during the embryo-to-hatchling transition. Furthermore, we know very little about the metabolic and regulatory factors that regulate lipid metabolism in late embryos or newly-hatched chicks. In the present study, we examined hepatic transcriptomes of 12 embryos and 12 hatchling chicks during the peri-hatch period—or the metabolic switch from chorioallantoic to pulmonary respiration. RESULTS: Initial hierarchical clustering revealed two distinct, albeit opposing, patterns of hepatic gene expression. Cluster A genes are largely lipolytic and highly expressed in embryos. While, Cluster B genes are lipogenic/thermogenic and mainly controlled by the lipogenic transcription factor THRSPA. Using pairwise comparisons of embryo and hatchling ages, we found 1272 genes that were differentially expressed between embryos and hatchling chicks, including 24 transcription factors and 284 genes that regulate lipid metabolism. The three most differentially-expressed transcripts found in liver of embryos were MOGAT1, DIO3 and PDK4, whereas THRSPA, FASN and DIO2 were highest in hatchlings. An unusual finding was the “ectopic” and extremely high differentially expression of seven feather keratin transcripts in liver of 16 day embryos, which coincides with engorgement of liver with yolk lipids. Gene interaction networks show several transcription factors, transcriptional co-activators/co-inhibitors and their downstream genes that exert a ‘ying-yang’ action on lipid metabolism during the embryo-to-hatching transition. These upstream regulators include ligand-activated transcription factors, sirtuins and Kruppel-like factors. CONCLUSIONS: Our genome-wide transcriptional analysis has greatly expanded the hepatic repertoire of regulatory and metabolic genes involved in the embryo-to-hatchling transition. New knowledge was gained on interactive transcriptional networks and metabolic pathways that enable the abrupt switch from ectothermy (embryo) to endothermy (hatchling) in the chicken. Several transcription factors and their coactivators/co-inhibitors appear to exert opposing actions on lipid metabolism, leading to the predominance of lipolysis in embryos and lipogenesis in hatchlings. Our analysis of hepatic transcriptomes has enabled discovery of opposing, interconnected and interdependent transcriptional regulators that provide precise ying-yang or homeorhetic regulation of lipid metabolism during the critical embryo-to-hatchling transition. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12864-018-5080-4) contains supplementary material, which is available to authorized users. BioMed Central 2018-09-21 /pmc/articles/PMC6151027/ /pubmed/30241500 http://dx.doi.org/10.1186/s12864-018-5080-4 Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. 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.
spellingShingle Research Article
Cogburn, Larry A.
Trakooljul, Nares
Chen, Chuming
Huang, Hongzhan
Wu, Cathy H.
Carré, Wilfrid
Wang, Xiaofei
White, Harold B.
Transcriptional profiling of liver during the critical embryo-to-hatchling transition period in the chicken (Gallus gallus)
title Transcriptional profiling of liver during the critical embryo-to-hatchling transition period in the chicken (Gallus gallus)
title_full Transcriptional profiling of liver during the critical embryo-to-hatchling transition period in the chicken (Gallus gallus)
title_fullStr Transcriptional profiling of liver during the critical embryo-to-hatchling transition period in the chicken (Gallus gallus)
title_full_unstemmed Transcriptional profiling of liver during the critical embryo-to-hatchling transition period in the chicken (Gallus gallus)
title_short Transcriptional profiling of liver during the critical embryo-to-hatchling transition period in the chicken (Gallus gallus)
title_sort transcriptional profiling of liver during the critical embryo-to-hatchling transition period in the chicken (gallus gallus)
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6151027/
https://www.ncbi.nlm.nih.gov/pubmed/30241500
http://dx.doi.org/10.1186/s12864-018-5080-4
work_keys_str_mv AT cogburnlarrya transcriptionalprofilingofliverduringthecriticalembryotohatchlingtransitionperiodinthechickengallusgallus
AT trakooljulnares transcriptionalprofilingofliverduringthecriticalembryotohatchlingtransitionperiodinthechickengallusgallus
AT chenchuming transcriptionalprofilingofliverduringthecriticalembryotohatchlingtransitionperiodinthechickengallusgallus
AT huanghongzhan transcriptionalprofilingofliverduringthecriticalembryotohatchlingtransitionperiodinthechickengallusgallus
AT wucathyh transcriptionalprofilingofliverduringthecriticalembryotohatchlingtransitionperiodinthechickengallusgallus
AT carrewilfrid transcriptionalprofilingofliverduringthecriticalembryotohatchlingtransitionperiodinthechickengallusgallus
AT wangxiaofei transcriptionalprofilingofliverduringthecriticalembryotohatchlingtransitionperiodinthechickengallusgallus
AT whiteharoldb transcriptionalprofilingofliverduringthecriticalembryotohatchlingtransitionperiodinthechickengallusgallus