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Registro Completo |
Biblioteca(s): |
Embrapa Agricultura Digital; Embrapa Pecuária Sudeste. |
Data corrente: |
27/05/2022 |
Data da última atualização: |
20/06/2022 |
Tipo da produção científica: |
Artigo em Periódico Indexado |
Autoria: |
SOUZA, M. M. de; NICIURA, S. C. M.; ROCHA, M. I. P.; PAN, Z.; ZHOU, H.; BRUSCADIN, J. J.; DINIZ, W. J. da S.; AFONSO, J.; OLIVEIRA, P. S. N. de; MOURÃO, G. B.; ZERLOTINI NETO, A.; COUTINHO, L. L.; KOLTES, J. E.; REGITANO, L. C. de A. |
Afiliação: |
MARCELA MARIA DE SOUZA, IOWA STATE UNIVERSITY; SIMONE CRISTINA MEO NICIURA, CPPSE; MARINA IBELLI PEREIRA ROCHA, UFSCAR; ZHANGYUAN PAN, UNIVERSITY OF CALIFORNIA; HUAIJUN ZHOU, UNIVERSITY OF CALIFORNIA; JENNIFER JESSICA BRUSCADIN, UFSCAR; WELLISON JARLES DA SILVA DINIZ, AUBURN UNIVERSITY; JULIANA AFONSO; PRISCILA SILVA NEUBERN DE OLIVEIRA, UFSCAR; GERSON B. MOURÃO, ESALQ/USP; ADHEMAR ZERLOTINI NETO, CNPTIA; LUIZ LEHMANN COUTINHO, ESALQ/USP; JAMES E. KOLTES, IOWA STATE UNIVERSITY; LUCIANA CORREIA DE ALMEIDA REGITANO, CPPSE. |
Título: |
DNA methylation may affect beef tenderness through signal transduction in Bos indicus. |
Ano de publicação: |
2022 |
Fonte/Imprenta: |
Epigenetics & Chromatin, v. 15, n. 1, p. 1-16, 2022. |
DOI: |
https://doi.org/10.1186/s13072-022-00449-4 |
Idioma: |
Inglês |
Notas: |
Article number: 15. |
Conteúdo: |
Abstract. Background:Beef tenderness is a complex trait of economic importance for the beef industry. Understanding the epigenetic mechanisms underlying this trait may help improve the accuracy of breeding programs. However, little is known about epigenetic effects on Bos taurus muscle and their implications in tenderness, and no studies have been conducted in Bos indicus.Results:Comparing methylation profile of Bos indicus skeletal muscle with contrasting beef tenderness at 14 days after slaughter, we identified differentially methylated cytosines and regions associated with this trait. Interestingly, muscle that became tender beef had higher levels of hypermethylation compared to the tough group. Enrichment analysis of predicted target genes suggested that differences in methylation between tender and tough beef may affect signal transduction pathways, among which G protein signaling was a key pathway. In addition, different meth-ylation levels were found associated with expression levels of GNAS, PDE4B, EPCAM and EBF3 genes. The differentially methylated elements correlated with EBF3 and GNAS genes overlapped CpG islands and regulatory elements. GNAS, a complex imprinted gene, has a key role on G protein signaling pathways. Moreover, both G protein signaling pathway and the EBF3 gene regulate muscle homeostasis, relaxation, and muscle cell-specificity.Conclusions:We present differentially methylated loci that may be of interest to decipher the epigenetic mecha-nisms affecting tenderness. Supported by the previous knowledge about regulatory elements and gene function, the methylation data suggests EBF3 and GNAS as potential candidate genes and G protein signaling as potential candi-date pathway associated with beef tenderness via methylation. MenosAbstract. Background:Beef tenderness is a complex trait of economic importance for the beef industry. Understanding the epigenetic mechanisms underlying this trait may help improve the accuracy of breeding programs. However, little is known about epigenetic effects on Bos taurus muscle and their implications in tenderness, and no studies have been conducted in Bos indicus.Results:Comparing methylation profile of Bos indicus skeletal muscle with contrasting beef tenderness at 14 days after slaughter, we identified differentially methylated cytosines and regions associated with this trait. Interestingly, muscle that became tender beef had higher levels of hypermethylation compared to the tough group. Enrichment analysis of predicted target genes suggested that differences in methylation between tender and tough beef may affect signal transduction pathways, among which G protein signaling was a key pathway. In addition, different meth-ylation levels were found associated with expression levels of GNAS, PDE4B, EPCAM and EBF3 genes. The differentially methylated elements correlated with EBF3 and GNAS genes overlapped CpG islands and regulatory elements. GNAS, a complex imprinted gene, has a key role on G protein signaling pathways. Moreover, both G protein signaling pathway and the EBF3 gene regulate muscle homeostasis, relaxation, and muscle cell-specificity.Conclusions:We present differentially methylated loci that may be of interest to decipher the epigenetic mecha-nisms affec... Mostrar Tudo |
Palavras-Chave: |
EBF3; Epigenoma; Epigenome; Força de cisalhamento; GNAS; Muscle; Músculo de nelore; Nelore; RRBS; Shear force. |
Thesagro: |
Bos Indicus; Bos Taurus; Metilação; Músculo. |
Thesaurus Nal: |
Cattle; DNA methylation; Methylation. |
Categoria do assunto: |
-- X Pesquisa, Tecnologia e Engenharia |
URL: |
https://ainfo.cnptia.embrapa.br/digital/bitstream/doc/1144144/1/DNA-MethylationMay.pdf
|
Marc: |
LEADER 03129naa a2200505 a 4500 001 2144144 005 2022-06-20 008 2022 bl uuuu u00u1 u #d 024 7 $ahttps://doi.org/10.1186/s13072-022-00449-4$2DOI 100 1 $aSOUZA, M. M. de 245 $aDNA methylation may affect beef tenderness through signal transduction in Bos indicus.$h[electronic resource] 260 $c2022 500 $aArticle number: 15. 520 $aAbstract. Background:Beef tenderness is a complex trait of economic importance for the beef industry. Understanding the epigenetic mechanisms underlying this trait may help improve the accuracy of breeding programs. However, little is known about epigenetic effects on Bos taurus muscle and their implications in tenderness, and no studies have been conducted in Bos indicus.Results:Comparing methylation profile of Bos indicus skeletal muscle with contrasting beef tenderness at 14 days after slaughter, we identified differentially methylated cytosines and regions associated with this trait. Interestingly, muscle that became tender beef had higher levels of hypermethylation compared to the tough group. Enrichment analysis of predicted target genes suggested that differences in methylation between tender and tough beef may affect signal transduction pathways, among which G protein signaling was a key pathway. In addition, different meth-ylation levels were found associated with expression levels of GNAS, PDE4B, EPCAM and EBF3 genes. The differentially methylated elements correlated with EBF3 and GNAS genes overlapped CpG islands and regulatory elements. GNAS, a complex imprinted gene, has a key role on G protein signaling pathways. Moreover, both G protein signaling pathway and the EBF3 gene regulate muscle homeostasis, relaxation, and muscle cell-specificity.Conclusions:We present differentially methylated loci that may be of interest to decipher the epigenetic mecha-nisms affecting tenderness. Supported by the previous knowledge about regulatory elements and gene function, the methylation data suggests EBF3 and GNAS as potential candidate genes and G protein signaling as potential candi-date pathway associated with beef tenderness via methylation. 650 $aCattle 650 $aDNA methylation 650 $aMethylation 650 $aBos Indicus 650 $aBos Taurus 650 $aMetilação 650 $aMúsculo 653 $aEBF3 653 $aEpigenoma 653 $aEpigenome 653 $aForça de cisalhamento 653 $aGNAS 653 $aMuscle 653 $aMúsculo de nelore 653 $aNelore 653 $aRRBS 653 $aShear force 700 1 $aNICIURA, S. C. M. 700 1 $aROCHA, M. I. P. 700 1 $aPAN, Z. 700 1 $aZHOU, H. 700 1 $aBRUSCADIN, J. J. 700 1 $aDINIZ, W. J. da S. 700 1 $aAFONSO, J. 700 1 $aOLIVEIRA, P. S. N. de 700 1 $aMOURÃO, G. B. 700 1 $aZERLOTINI NETO, A. 700 1 $aCOUTINHO, L. L. 700 1 $aKOLTES, J. E. 700 1 $aREGITANO, L. C. de A. 773 $tEpigenetics & Chromatin$gv. 15, n. 1, p. 1-16, 2022.
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Registro original: |
Embrapa Pecuária Sudeste (CPPSE) |
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Registros recuperados : 53 | |
4. | | AMARAL, A. M. do; HOMEM, R. A.; MACHADO, M. A. Expressão de genes de Xanthomonas axonopodis pv. citri através de interação com a planta de citros. Fitopatologia Brasileira, Brasília, DF, v. 32, supl., p. S247, ago. 2007. Resumo 0692. Edição dos Resumos do XL Congresso Brasileiro de Fitopatologia, Maringá, PR, ago. 2007.Tipo: Resumo em Anais de Congresso |
Biblioteca(s): Embrapa Recursos Genéticos e Biotecnologia. |
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5. | | HOMEM, R. A.; BAPTISTA, J. C.; AMARAL, A. M. do; MACHADO, M. A. Análise mutacional de Xanthomonas axonopodis pv. citri para componentes do sistema de secreção tipo III. Summa Phytopathologica, Botucatu, v. 33, supl., p. S14, 2007. Resumo 020. Edição dos Anais do XXX Congresso Paulista de Fitopatologia, 2007, Jaboticabal.Tipo: Resumo em Anais de Congresso |
Biblioteca(s): Embrapa Recursos Genéticos e Biotecnologia. |
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11. | | MACHADO, M. A.; ÁSTUA, J. F.; AMARAL, A. M. do; MALOSSO, A.; MAZZAFERA, P. Gene expression of carotenoid biosynthesis pathway and carotenoid content in different varieties of sweet orange (Citrus sinensis L. Osb.). In: INTERNATIONAL CITRUS CONGRESS, 11., 2008, Wuhan,China. Program and abstracts... Wuhan: The International Society of Citriculture, 2008. p. 60. 105.Tipo: Resumo em Anais de Congresso |
Biblioteca(s): Embrapa Mandioca e Fruticultura. |
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14. | | AMARAL, A. M. do; DOMINGUES, A. D.; MACHADO, M. A.; CARVALHO, S. A. de. Resposta ao cancro cítrico, em casa-de-vegetação, de plantas de citros de variedades com potencial uso comercial. Fitopatologia Brasileira, Brasília, DF, v. 29, p. S242, ago. 2004. Edição dos Resumos do XXXVII Congresso Brasileiro de Fitopatologia, Gramado, RS, ago. 2004.Tipo: Resumo em Anais de Congresso |
Biblioteca(s): Embrapa Recursos Genéticos e Biotecnologia. |
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17. | | AMARAL, A. M. do; BAPTISTA, J. C.; SOUZA, C. B. de; RONCOLETTA, J. G. T.; MACHADO, M. A. Adaptação patógeno-hospedeiro e virulência de mutante de Xanthomonas axonopodis pv. citri defectivo para produção de pigmento. Fitopatologia Brasileira, Brasília, DF, v. 29, p. S253, ago. 2004. Edição dos Resumos do XXXVII Congresso Brasileiro de Fitopatologia, Gramado, RS, ago. 2004.Tipo: Resumo em Anais de Congresso |
Biblioteca(s): Embrapa Recursos Genéticos e Biotecnologia. |
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18. | | CARVALHO, S. A.; CROCE-FLIHO, J.; NUNES, W. M.; AMARAL, A. M. do; SILVA, L. F. C.; MACHADO, M. A. Avaliação da resistência ao cancro cítrico em germoplasma de citros em condições de campo. Fitopatologia Brasileira, v. 30, supl., ago., 2005.Biblioteca(s): Embrapa Recursos Genéticos e Biotecnologia. |
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19. | | NAKATANI, A. K.; AMARAL, A. M. do; BRIGANTI, L. E. R. P. P. L. D. B.; MACHADO, M. A. Método de purificação de DNA de Candidatus Liberibacter spp., agente causal de huanglongbing (ex-greening) dos citros, a partir de material vegetal infectado. In: CONGRESSO BRASILEIRO DE GENÉTICA, 53., 2007, Águas de Lindóia. Resumos... Águas de Lindóia: Sociedade Brasileira de Genética, 2007. p. 26Tipo: Resumo em Anais de Congresso |
Biblioteca(s): Embrapa Recursos Genéticos e Biotecnologia. |
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20. | | BOSCARIOL-CAMARGO, R. L.; SIMÔES, T. S.; DEZOTTI, D. F.; HARAKAVA, R.; AMARAL, A. M. do; MACHADO, M. A. Transformação genética de laranjas doces visando resistência à CVC. In: CONGRESSO BRASILEIRO DE GENÉTICA, 51., 2005, Águas de Lindóia, SP. A era da genômica: da bioestatística à bioinformática: anais. Ribeirão Preto, SP: Sociedade Brasileira de Genética, 2005. p. 448.Biblioteca(s): Embrapa Recursos Genéticos e Biotecnologia. |
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