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Registro Completo |
Biblioteca(s): |
Embrapa Meio-Norte; Embrapa Rondônia; Embrapa Semiárido. |
Data corrente: |
21/11/2017 |
Data da última atualização: |
27/11/2017 |
Autoria: |
LEITE, P. R. de M.; SANTIAGO, A. A.; NAVARRO FILHO, H. R.; ALBUQUERQUE, R. P. de F.; LEITE, R. de M. H.; GUEDES, P. L. C.; BACALHAU, A. dos S.; LIMA, A. M. de. |
Título: |
Sindi: gado vermelho para o semiárido. |
Edição: |
2.ed.rev.ampl. |
Ano de publicação: |
2017 |
Fonte/Imprenta: |
João Pessoa, PB: EMEPA, 2017 |
Páginas: |
196p. |
Descrição Física: |
il. color. |
ISBN: |
978-85-65808-07-1 |
Idioma: |
Português |
Conteúdo: |
Sumário: Prefácio; Apresentação da 1ª Edição; Homenagens; Nota aos leitores. 1. A Raça Sindi da Índia e do Paquistão; 2. A história da entrada do gado Sindi no Brasil; 3. Expansão do gado Sindi no Brasil; 4. Divulgação do gado Sindi na Região Nordeste; 5. Criação do gado Sindi da EMEPA-PB; 6. Formação e recuperação do registro PO do Gado Sindi da EMEPA-PB e da Embrapa. |
Palavras-Chave: |
Bovine; Bovine milk; Desenvolvimento ponderal; Embrapa; Emepa; Formação do rebanho; Gado vermelho; Origem da Índia; Origem do Paquistão; PO do Gado Sindi; Semiárido; Sindi cattle. |
Thesagro: |
Bovino; Gado de Corte; Gado Leiteiro; Gado Sindi. |
Thesaurus Nal: |
Beef cattle. |
Categoria do assunto: |
L Ciência Animal e Produtos de Origem Animal |
Marc: |
LEADER 01515nam a2200433 a 4500 001 2080817 005 2017-11-27 008 2017 bl uuuu 00u1 u #d 020 $a978-85-65808-07-1 100 1 $aLEITE, P. R. de M. 245 $aSindi$bgado vermelho para o semiárido. 250 $a2.ed.rev.ampl. 260 $aJoão Pessoa, PB: EMEPA$c2017 300 $a196p.$cil. color. 520 $aSumário: Prefácio; Apresentação da 1ª Edição; Homenagens; Nota aos leitores. 1. A Raça Sindi da Índia e do Paquistão; 2. A história da entrada do gado Sindi no Brasil; 3. Expansão do gado Sindi no Brasil; 4. Divulgação do gado Sindi na Região Nordeste; 5. Criação do gado Sindi da EMEPA-PB; 6. Formação e recuperação do registro PO do Gado Sindi da EMEPA-PB e da Embrapa. 650 $aBeef cattle 650 $aBovino 650 $aGado de Corte 650 $aGado Leiteiro 650 $aGado Sindi 653 $aBovine 653 $aBovine milk 653 $aDesenvolvimento ponderal 653 $aEmbrapa 653 $aEmepa 653 $aFormação do rebanho 653 $aGado vermelho 653 $aOrigem da Índia 653 $aOrigem do Paquistão 653 $aPO do Gado Sindi 653 $aSemiárido 653 $aSindi cattle 700 1 $aSANTIAGO, A. A. 700 1 $aNAVARRO FILHO, H. R. 700 1 $aALBUQUERQUE, R. P. de F. 700 1 $aLEITE, R. de M. H. 700 1 $aGUEDES, P. L. C. 700 1 $aBACALHAU, A. dos S. 700 1 $aLIMA, A. M. de
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Registro original: |
Embrapa Rondônia (CPAF-RO) |
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Registro Completo
Biblioteca(s): |
Embrapa Pecuária Sudeste. |
Data corrente: |
19/02/2019 |
Data da última atualização: |
19/02/2019 |
Tipo da produção científica: |
Artigo em Periódico Indexado |
Circulação/Nível: |
A - 1 |
Autoria: |
POLETI, M. D.; REGITANO, L. C. de A.; SOUSA, G. H. M. F.; CESAR, A. S. M.; SIMAS, R. C.; SILVA-VIGNATO, B.; OLIVEIRA, G. B.; ANDRADE, S. C. S.; CAMERON, L. C.; COUTINHO, L. L. |
Afiliação: |
Mirele D. Poleti, USP; LUCIANA CORREIA DE ALMEIDA REGITANO, CPPSE; Gustavo H. M. F. Souza, MS Applications and Development Laboratory Waters Corporation; Aline S. M. Cesar, USP; Rosineide C. Simas, USP; Bárbara Silva-Vignato, USP; Gabriella B. Oliveira, USP; Sónia C. S. Andrade, USP; Luiz C. Cameron, UNIRIO; Luiz Lehmann Coutinho, USP. |
Título: |
Longissimus dorsi muscle label-free quantitative proteomic reveals biological mechanisms associated with intramuscular fat deposition. |
Ano de publicação: |
2018 |
Fonte/Imprenta: |
Journal of Proteomics, v. 179, p. 30-41, 2018. |
DOI: |
https://doi.org/10.1016/j.dib.2018.06.004 |
Idioma: |
Inglês |
Conteúdo: |
The pathways involved in intramuscular fat (IMF) deposition in Longissimus dorsi muscle were investigated using an integrated transcriptome-assisted label-free quantitative proteomic approach by High Definition Mass Spectrometry. We quantified 1582 proteins, of which 164 were differentially abundant proteins (DAPs, p < 0.05) between animals with high (H) and low (L) genomic estimated breeding values (GEBV) for IMF content. Ingenuity pathway analysis (IPA) revealed that these DAPs were mainly involved in glycolysis metabolism, actin cytoskeleton signaling, cell-cell adherens junction and pathways for MAPK and insulin. A comparative study between transcriptomic (mRNA) and proteomic data showed 17 differentially expressed genes corresponding to DAPs, of which three genes/proteins did not agree on the direction of the fold change between groups. Moreover, we investigated microRNAs data to explain these differences in fold change direction, being able to unravel two of the three unexpected mRNA/protein relationships. Results demonstrated that changes in protein/mRNA levels of sarcomere organization, intracellular signal transduction and regulation of actin cytoskeleton, are involved in IMF deposition. These findings provide a deeper understanding of the highly complex regulatory mechanisms involved in IMF deposition in cattle and indicate target pathways for future studies. Significance: Intramuscular fat is the amount of fat deposited inside muscle and plays an important role in human health and meat quality attributes, influencing energy metabolism of skeletal muscle, as well as, tenderness, flavor, and juiciness of beef. We performed for the first time the utilization of integrated transcriptome-assisted label-free quantitative proteomic approach using High Definition Mass Spectrometry for characterization of the changes in the proteomic profile of the Longissimus dorsi muscle associated with intramuscular fat deposition in cattle. Furthermore, we compared the muscle proteome with the muscle transcriptome (mRNA and microRNAs), obtained by RNA-sequencing, to better understand the relationship between expression of mRNAs and proteins and to unravel essential biological mechanisms involved in bovine skeletal muscle IMF deposition. MenosThe pathways involved in intramuscular fat (IMF) deposition in Longissimus dorsi muscle were investigated using an integrated transcriptome-assisted label-free quantitative proteomic approach by High Definition Mass Spectrometry. We quantified 1582 proteins, of which 164 were differentially abundant proteins (DAPs, p < 0.05) between animals with high (H) and low (L) genomic estimated breeding values (GEBV) for IMF content. Ingenuity pathway analysis (IPA) revealed that these DAPs were mainly involved in glycolysis metabolism, actin cytoskeleton signaling, cell-cell adherens junction and pathways for MAPK and insulin. A comparative study between transcriptomic (mRNA) and proteomic data showed 17 differentially expressed genes corresponding to DAPs, of which three genes/proteins did not agree on the direction of the fold change between groups. Moreover, we investigated microRNAs data to explain these differences in fold change direction, being able to unravel two of the three unexpected mRNA/protein relationships. Results demonstrated that changes in protein/mRNA levels of sarcomere organization, intracellular signal transduction and regulation of actin cytoskeleton, are involved in IMF deposition. These findings provide a deeper understanding of the highly complex regulatory mechanisms involved in IMF deposition in cattle and indicate target pathways for future studies. Significance: Intramuscular fat is the amount of fat deposited inside muscle and plays an important role in... Mostrar Tudo |
Palavras-Chave: |
Adiposidade; Gordura intramuscular; MRNA. |
Thesagro: |
Gordura Animal. |
Thesaurus NAL: |
Mass spectrometry; MicroRNA. |
Categoria do assunto: |
L Ciência Animal e Produtos de Origem Animal |
Marc: |
LEADER 03231naa a2200313 a 4500 001 2106242 005 2019-02-19 008 2018 bl uuuu u00u1 u #d 024 7 $ahttps://doi.org/10.1016/j.dib.2018.06.004$2DOI 100 1 $aPOLETI, M. D. 245 $aLongissimus dorsi muscle label-free quantitative proteomic reveals biological mechanisms associated with intramuscular fat deposition.$h[electronic resource] 260 $c2018 520 $aThe pathways involved in intramuscular fat (IMF) deposition in Longissimus dorsi muscle were investigated using an integrated transcriptome-assisted label-free quantitative proteomic approach by High Definition Mass Spectrometry. We quantified 1582 proteins, of which 164 were differentially abundant proteins (DAPs, p < 0.05) between animals with high (H) and low (L) genomic estimated breeding values (GEBV) for IMF content. Ingenuity pathway analysis (IPA) revealed that these DAPs were mainly involved in glycolysis metabolism, actin cytoskeleton signaling, cell-cell adherens junction and pathways for MAPK and insulin. A comparative study between transcriptomic (mRNA) and proteomic data showed 17 differentially expressed genes corresponding to DAPs, of which three genes/proteins did not agree on the direction of the fold change between groups. Moreover, we investigated microRNAs data to explain these differences in fold change direction, being able to unravel two of the three unexpected mRNA/protein relationships. Results demonstrated that changes in protein/mRNA levels of sarcomere organization, intracellular signal transduction and regulation of actin cytoskeleton, are involved in IMF deposition. These findings provide a deeper understanding of the highly complex regulatory mechanisms involved in IMF deposition in cattle and indicate target pathways for future studies. Significance: Intramuscular fat is the amount of fat deposited inside muscle and plays an important role in human health and meat quality attributes, influencing energy metabolism of skeletal muscle, as well as, tenderness, flavor, and juiciness of beef. We performed for the first time the utilization of integrated transcriptome-assisted label-free quantitative proteomic approach using High Definition Mass Spectrometry for characterization of the changes in the proteomic profile of the Longissimus dorsi muscle associated with intramuscular fat deposition in cattle. Furthermore, we compared the muscle proteome with the muscle transcriptome (mRNA and microRNAs), obtained by RNA-sequencing, to better understand the relationship between expression of mRNAs and proteins and to unravel essential biological mechanisms involved in bovine skeletal muscle IMF deposition. 650 $aMass spectrometry 650 $aMicroRNA 650 $aGordura Animal 653 $aAdiposidade 653 $aGordura intramuscular 653 $aMRNA 700 1 $aREGITANO, L. C. de A. 700 1 $aSOUSA, G. H. M. F. 700 1 $aCESAR, A. S. M. 700 1 $aSIMAS, R. C. 700 1 $aSILVA-VIGNATO, B. 700 1 $aOLIVEIRA, G. B. 700 1 $aANDRADE, S. C. S. 700 1 $aCAMERON, L. C. 700 1 $aCOUTINHO, L. L. 773 $tJournal of Proteomics$gv. 179, p. 30-41, 2018.
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