Cargando…
Proteomics reveals changes in hepatic proteins during chicken embryonic development: an alternative model to study human obesity
BACKGROUND: Chicken embryos are widely used as a model for studies of obesity; however, no detailed information is available about the dynamic changes of proteins during the regulation of adipose biology and metabolism. Thus, the present study used an isobaric tags for relative and absolute quantita...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5759888/ https://www.ncbi.nlm.nih.gov/pubmed/29310583 http://dx.doi.org/10.1186/s12864-017-4427-6 |
_version_ | 1783291290593525760 |
---|---|
author | Peng, Mengling Li, Shengnan He, Qianian Zhao, Jinlong Li, Longlong Ma, Haitian |
author_facet | Peng, Mengling Li, Shengnan He, Qianian Zhao, Jinlong Li, Longlong Ma, Haitian |
author_sort | Peng, Mengling |
collection | PubMed |
description | BACKGROUND: Chicken embryos are widely used as a model for studies of obesity; however, no detailed information is available about the dynamic changes of proteins during the regulation of adipose biology and metabolism. Thus, the present study used an isobaric tags for relative and absolute quantitation (iTRAQ)-based proteomic approach to identify the changes in protein abundance at different stages of chicken embryonic development. RESULTS: In this study, the abundances of 293 hepatic proteins in 19-day old of chicken embryos compared with 14-day old and 160 hepatic proteins at hatching compared with 19-day old embryos were significantly changed. Pathway analysis showed that fatty acid degradation (upregulated ACAA2, CPT1A, and ACOX1), protein folding (upregulated PDIs, CALR3, LMAN1, and UBQLN1) and gluconeogenesis (upregulated ACSS1, AKR1A1, ALDH3A2, ALDH7A1, and FBP2) were enhanced from embryonic day 14 (E14) to E19 of chicken embryo development. Analysis of the differentially abundant proteins indicated that glycolysis was not the main way to produce energy from E19 to hatching day during chicken embryo development. In addition, purine metabolism was enhanced, as deduced from increased IMPDH2, NT5C, PGM2, and XDH abundances, and the decrease of growth rate could be overcome by increasing the abundance of ribosomal proteins from E19 to the hatching day. CONCLUSION: The levels of certain proteins were coordinated with each other to regulate the changes in metabolic pathways to satisfy the requirement for growth and development at different stages of chicken embryo development. Importantly, ACAA2, CPT1A, and ACOX1 might be key factors to control fat deposition during chicken embryonic development. These results provided information showing that chicken is a useful model to further investigate the mechanism of obesity and insulin resistance in humans. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12864-017-4427-6) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5759888 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-57598882018-01-16 Proteomics reveals changes in hepatic proteins during chicken embryonic development: an alternative model to study human obesity Peng, Mengling Li, Shengnan He, Qianian Zhao, Jinlong Li, Longlong Ma, Haitian BMC Genomics Research Article BACKGROUND: Chicken embryos are widely used as a model for studies of obesity; however, no detailed information is available about the dynamic changes of proteins during the regulation of adipose biology and metabolism. Thus, the present study used an isobaric tags for relative and absolute quantitation (iTRAQ)-based proteomic approach to identify the changes in protein abundance at different stages of chicken embryonic development. RESULTS: In this study, the abundances of 293 hepatic proteins in 19-day old of chicken embryos compared with 14-day old and 160 hepatic proteins at hatching compared with 19-day old embryos were significantly changed. Pathway analysis showed that fatty acid degradation (upregulated ACAA2, CPT1A, and ACOX1), protein folding (upregulated PDIs, CALR3, LMAN1, and UBQLN1) and gluconeogenesis (upregulated ACSS1, AKR1A1, ALDH3A2, ALDH7A1, and FBP2) were enhanced from embryonic day 14 (E14) to E19 of chicken embryo development. Analysis of the differentially abundant proteins indicated that glycolysis was not the main way to produce energy from E19 to hatching day during chicken embryo development. In addition, purine metabolism was enhanced, as deduced from increased IMPDH2, NT5C, PGM2, and XDH abundances, and the decrease of growth rate could be overcome by increasing the abundance of ribosomal proteins from E19 to the hatching day. CONCLUSION: The levels of certain proteins were coordinated with each other to regulate the changes in metabolic pathways to satisfy the requirement for growth and development at different stages of chicken embryo development. Importantly, ACAA2, CPT1A, and ACOX1 might be key factors to control fat deposition during chicken embryonic development. These results provided information showing that chicken is a useful model to further investigate the mechanism of obesity and insulin resistance in humans. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12864-017-4427-6) contains supplementary material, which is available to authorized users. BioMed Central 2018-01-08 /pmc/articles/PMC5759888/ /pubmed/29310583 http://dx.doi.org/10.1186/s12864-017-4427-6 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 Peng, Mengling Li, Shengnan He, Qianian Zhao, Jinlong Li, Longlong Ma, Haitian Proteomics reveals changes in hepatic proteins during chicken embryonic development: an alternative model to study human obesity |
title | Proteomics reveals changes in hepatic proteins during chicken embryonic development: an alternative model to study human obesity |
title_full | Proteomics reveals changes in hepatic proteins during chicken embryonic development: an alternative model to study human obesity |
title_fullStr | Proteomics reveals changes in hepatic proteins during chicken embryonic development: an alternative model to study human obesity |
title_full_unstemmed | Proteomics reveals changes in hepatic proteins during chicken embryonic development: an alternative model to study human obesity |
title_short | Proteomics reveals changes in hepatic proteins during chicken embryonic development: an alternative model to study human obesity |
title_sort | proteomics reveals changes in hepatic proteins during chicken embryonic development: an alternative model to study human obesity |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5759888/ https://www.ncbi.nlm.nih.gov/pubmed/29310583 http://dx.doi.org/10.1186/s12864-017-4427-6 |
work_keys_str_mv | AT pengmengling proteomicsrevealschangesinhepaticproteinsduringchickenembryonicdevelopmentanalternativemodeltostudyhumanobesity AT lishengnan proteomicsrevealschangesinhepaticproteinsduringchickenembryonicdevelopmentanalternativemodeltostudyhumanobesity AT heqianian proteomicsrevealschangesinhepaticproteinsduringchickenembryonicdevelopmentanalternativemodeltostudyhumanobesity AT zhaojinlong proteomicsrevealschangesinhepaticproteinsduringchickenembryonicdevelopmentanalternativemodeltostudyhumanobesity AT lilonglong proteomicsrevealschangesinhepaticproteinsduringchickenembryonicdevelopmentanalternativemodeltostudyhumanobesity AT mahaitian proteomicsrevealschangesinhepaticproteinsduringchickenembryonicdevelopmentanalternativemodeltostudyhumanobesity |