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Identification and characterization of genes that control fat deposition in chickens

BACKGROUND: Fat deposits in chickens contribute significantly to meat quality attributes such as juiciness, flavor, taste and other organoleptic properties. The quantity of fat deposited increases faster and earlier in the fast-growing chickens than in slow-growing chickens. In this study, Affymetri...

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Autores principales: Claire D’Andre, Hirwa, Paul, Wallace, Shen, Xu, Jia, Xinzheng, Zhang, Rong, Sun, Liang, Zhang, Xiquan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3874612/
https://www.ncbi.nlm.nih.gov/pubmed/24206759
http://dx.doi.org/10.1186/2049-1891-4-43
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author Claire D’Andre, Hirwa
Paul, Wallace
Shen, Xu
Jia, Xinzheng
Zhang, Rong
Sun, Liang
Zhang, Xiquan
author_facet Claire D’Andre, Hirwa
Paul, Wallace
Shen, Xu
Jia, Xinzheng
Zhang, Rong
Sun, Liang
Zhang, Xiquan
author_sort Claire D’Andre, Hirwa
collection PubMed
description BACKGROUND: Fat deposits in chickens contribute significantly to meat quality attributes such as juiciness, flavor, taste and other organoleptic properties. The quantity of fat deposited increases faster and earlier in the fast-growing chickens than in slow-growing chickens. In this study, Affymetrix Genechip® Chicken Genome Arrays 32773 transcripts were used to compare gene expression profiles in liver and hypothalamus tissues of fast-growing and slow-growing chicken at 8 wk of age. Real-time RT-PCR was used to validate the differential expression of genes selected from the microarray analysis. The mRNA expression of the genes was further examined in fat tissues. The association of single nucleotide polymorphisms of four lipid-related genes with fat traits was examined in a F(2) resource population. RESULTS: Four hundred genes in the liver tissues and 220 genes hypothalamus tissues, respectively, were identified to be differentially expressed in fast-growing chickens and slow-growing chickens. Expression levels of genes for lipid metabolism (SULT1B1, ACSBG2, PNPLA3, LPL, AOAH) carbohydrate metabolism (MGAT4B, XYLB, GBE1, PGM1, HKDC1)cholesttrol biosynthesis (FDPS, LSS, HMGCR, NSDHL, DHCR24, IDI1, ME1) HSD17B7 and other reaction or processes (CYP1A4, CYP1A1, AKR1B1, CYP4V2, DDO) were higher in the fast-growing White Recessive Rock chickens than in the slow-growing Xinghua chickens. On the other hand, expression levels of genes associated with multicellular organism development, immune response, DNA integration, melanin biosynthetic process, muscle organ development and oxidation-reduction (FRZB, DMD, FUT8, CYP2C45, DHRSX, and CYP2C18) and with glycol-metabolism (GCNT2, ELOVL 6, and FASN), were higher in the XH chickens than in the fast-growing chickens. RT-PCR validated high expression levels of nine out of 12 genes in fat tissues. The G1257069A and T1247123C of the ACSBG2 gene were significantly associated with abdominal fat weight. The G4928024A of the FASN gene were significantly associated with fat bandwidth, and abdominal fat percentage. The C4930169T of the FASN gene was associated with abdominal fat weight while the A59539099G of the ELOVL 6 was significantly associated with subcutaneous fat. The A8378815G of the DDT was associated with fat band width. CONCLUSION: The differences in fat deposition were reflected with differential gene expressions in fast and slow growing chickens.
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spelling pubmed-38746122013-12-31 Identification and characterization of genes that control fat deposition in chickens Claire D’Andre, Hirwa Paul, Wallace Shen, Xu Jia, Xinzheng Zhang, Rong Sun, Liang Zhang, Xiquan J Anim Sci Biotechnol Research BACKGROUND: Fat deposits in chickens contribute significantly to meat quality attributes such as juiciness, flavor, taste and other organoleptic properties. The quantity of fat deposited increases faster and earlier in the fast-growing chickens than in slow-growing chickens. In this study, Affymetrix Genechip® Chicken Genome Arrays 32773 transcripts were used to compare gene expression profiles in liver and hypothalamus tissues of fast-growing and slow-growing chicken at 8 wk of age. Real-time RT-PCR was used to validate the differential expression of genes selected from the microarray analysis. The mRNA expression of the genes was further examined in fat tissues. The association of single nucleotide polymorphisms of four lipid-related genes with fat traits was examined in a F(2) resource population. RESULTS: Four hundred genes in the liver tissues and 220 genes hypothalamus tissues, respectively, were identified to be differentially expressed in fast-growing chickens and slow-growing chickens. Expression levels of genes for lipid metabolism (SULT1B1, ACSBG2, PNPLA3, LPL, AOAH) carbohydrate metabolism (MGAT4B, XYLB, GBE1, PGM1, HKDC1)cholesttrol biosynthesis (FDPS, LSS, HMGCR, NSDHL, DHCR24, IDI1, ME1) HSD17B7 and other reaction or processes (CYP1A4, CYP1A1, AKR1B1, CYP4V2, DDO) were higher in the fast-growing White Recessive Rock chickens than in the slow-growing Xinghua chickens. On the other hand, expression levels of genes associated with multicellular organism development, immune response, DNA integration, melanin biosynthetic process, muscle organ development and oxidation-reduction (FRZB, DMD, FUT8, CYP2C45, DHRSX, and CYP2C18) and with glycol-metabolism (GCNT2, ELOVL 6, and FASN), were higher in the XH chickens than in the fast-growing chickens. RT-PCR validated high expression levels of nine out of 12 genes in fat tissues. The G1257069A and T1247123C of the ACSBG2 gene were significantly associated with abdominal fat weight. The G4928024A of the FASN gene were significantly associated with fat bandwidth, and abdominal fat percentage. The C4930169T of the FASN gene was associated with abdominal fat weight while the A59539099G of the ELOVL 6 was significantly associated with subcutaneous fat. The A8378815G of the DDT was associated with fat band width. CONCLUSION: The differences in fat deposition were reflected with differential gene expressions in fast and slow growing chickens. BioMed Central 2013-11-09 /pmc/articles/PMC3874612/ /pubmed/24206759 http://dx.doi.org/10.1186/2049-1891-4-43 Text en Copyright © 2013 Claire D’Andre et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Claire D’Andre, Hirwa
Paul, Wallace
Shen, Xu
Jia, Xinzheng
Zhang, Rong
Sun, Liang
Zhang, Xiquan
Identification and characterization of genes that control fat deposition in chickens
title Identification and characterization of genes that control fat deposition in chickens
title_full Identification and characterization of genes that control fat deposition in chickens
title_fullStr Identification and characterization of genes that control fat deposition in chickens
title_full_unstemmed Identification and characterization of genes that control fat deposition in chickens
title_short Identification and characterization of genes that control fat deposition in chickens
title_sort identification and characterization of genes that control fat deposition in chickens
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3874612/
https://www.ncbi.nlm.nih.gov/pubmed/24206759
http://dx.doi.org/10.1186/2049-1891-4-43
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