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Identification of differentially expressed genes and pathways for intramuscular fat metabolism between breast and thigh tissues of chickens

BACKGROUND: Intramuscular fat (IMF) is one of the important factors influencing meat quality, however, for chickens, the molecular regulatory mechanisms underlying this trait have not yet been clear. In this study, a systematic identification of differentially expressed genes (DEGs) and molecular re...

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Autores principales: Cui, Huanxian, Zheng, Maiqing, Zhao, Guiping, Liu, Ranran, Wen, Jie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5771206/
https://www.ncbi.nlm.nih.gov/pubmed/29338766
http://dx.doi.org/10.1186/s12864-017-4292-3
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author Cui, Huanxian
Zheng, Maiqing
Zhao, Guiping
Liu, Ranran
Wen, Jie
author_facet Cui, Huanxian
Zheng, Maiqing
Zhao, Guiping
Liu, Ranran
Wen, Jie
author_sort Cui, Huanxian
collection PubMed
description BACKGROUND: Intramuscular fat (IMF) is one of the important factors influencing meat quality, however, for chickens, the molecular regulatory mechanisms underlying this trait have not yet been clear. In this study, a systematic identification of differentially expressed genes (DEGs) and molecular regulatory mechanism related to IMF metabolism between Beijing-you chicken breast and thigh at 42 and 90 days of age was performed. RESULTS: IMF contents, Gene Ontology (GO) terms, and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathways were analyzed, The results showed that both IMF contents in breast at 42 and 90 d were significantly lower (P < 0.05 or P < 0.01) than those in thigh. By microarray, 515 common known DEGs and 36 DEGs related to IMF metabolism were identified between the breast and thigh at 42 and 90 d. Compared to thigh, the expression levels of PPARG had significantly down-regulated (P < 0.01) in breast, but the expression levels of RXRA and CEBPB had significantly up-regulated (P < 0.01). However, the expression levels of LPL, FABP4, THRSP, RBP7, LDLR, FABP3, CPT2 and PPARGC1A had significantly down-regulated in breast (P < 0.01), supporting that PPARG and its down-stream genes had the important regulatory function to IMF deposition. In addition, based on of DEGs, KEGG analysis revealed that PPAR signaling pathway and cell junction-related pathways (focal adhesion and ECM-receptor interaction, which play a prominent role in maintaining the integrity of tissues), might contribute to the IMF metabolism in chicken. CONCLUSIONS: Our data had screened the potential candidate genes associated with chicken IMF metabolism, and imply that IMF metabolism in chicken is regulated and mediated not only by related functional genes and PPAR pathway, but also by others involved in cell junctions. These findings establish the groundwork and provide new clues for deciphering the molecular mechanisms underlying IMF deposition in poultry. Further studies at the translational and posttranslational level are now required to validate the genes and pathways identified here. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12864-017-4292-3) contains supplementary material, which is available to authorized users.
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spelling pubmed-57712062018-01-26 Identification of differentially expressed genes and pathways for intramuscular fat metabolism between breast and thigh tissues of chickens Cui, Huanxian Zheng, Maiqing Zhao, Guiping Liu, Ranran Wen, Jie BMC Genomics Research Article BACKGROUND: Intramuscular fat (IMF) is one of the important factors influencing meat quality, however, for chickens, the molecular regulatory mechanisms underlying this trait have not yet been clear. In this study, a systematic identification of differentially expressed genes (DEGs) and molecular regulatory mechanism related to IMF metabolism between Beijing-you chicken breast and thigh at 42 and 90 days of age was performed. RESULTS: IMF contents, Gene Ontology (GO) terms, and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathways were analyzed, The results showed that both IMF contents in breast at 42 and 90 d were significantly lower (P < 0.05 or P < 0.01) than those in thigh. By microarray, 515 common known DEGs and 36 DEGs related to IMF metabolism were identified between the breast and thigh at 42 and 90 d. Compared to thigh, the expression levels of PPARG had significantly down-regulated (P < 0.01) in breast, but the expression levels of RXRA and CEBPB had significantly up-regulated (P < 0.01). However, the expression levels of LPL, FABP4, THRSP, RBP7, LDLR, FABP3, CPT2 and PPARGC1A had significantly down-regulated in breast (P < 0.01), supporting that PPARG and its down-stream genes had the important regulatory function to IMF deposition. In addition, based on of DEGs, KEGG analysis revealed that PPAR signaling pathway and cell junction-related pathways (focal adhesion and ECM-receptor interaction, which play a prominent role in maintaining the integrity of tissues), might contribute to the IMF metabolism in chicken. CONCLUSIONS: Our data had screened the potential candidate genes associated with chicken IMF metabolism, and imply that IMF metabolism in chicken is regulated and mediated not only by related functional genes and PPAR pathway, but also by others involved in cell junctions. These findings establish the groundwork and provide new clues for deciphering the molecular mechanisms underlying IMF deposition in poultry. Further studies at the translational and posttranslational level are now required to validate the genes and pathways identified here. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12864-017-4292-3) contains supplementary material, which is available to authorized users. BioMed Central 2018-01-16 /pmc/articles/PMC5771206/ /pubmed/29338766 http://dx.doi.org/10.1186/s12864-017-4292-3 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
Cui, Huanxian
Zheng, Maiqing
Zhao, Guiping
Liu, Ranran
Wen, Jie
Identification of differentially expressed genes and pathways for intramuscular fat metabolism between breast and thigh tissues of chickens
title Identification of differentially expressed genes and pathways for intramuscular fat metabolism between breast and thigh tissues of chickens
title_full Identification of differentially expressed genes and pathways for intramuscular fat metabolism between breast and thigh tissues of chickens
title_fullStr Identification of differentially expressed genes and pathways for intramuscular fat metabolism between breast and thigh tissues of chickens
title_full_unstemmed Identification of differentially expressed genes and pathways for intramuscular fat metabolism between breast and thigh tissues of chickens
title_short Identification of differentially expressed genes and pathways for intramuscular fat metabolism between breast and thigh tissues of chickens
title_sort identification of differentially expressed genes and pathways for intramuscular fat metabolism between breast and thigh tissues of chickens
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5771206/
https://www.ncbi.nlm.nih.gov/pubmed/29338766
http://dx.doi.org/10.1186/s12864-017-4292-3
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