Data/hora: 19/06/2024 21:48:43

Biblioteca(s): | Embrapa Agricultura Digital; Embrapa Pecuária Sul.
Data corrente: | 02/01/2014
Data da última atualização: | 22/01/2020
Autoria: | GIACHETTO, P. F.; PEREIRA, F. C. P.; MOKRY, F. B.; HIGA, R. H.; MUDADU, M. A.; SILVA, M. V.; NICIURA, S. C. M.; CARDOSO, F. F.; ALENCAR, M. M.; MEIRELLES, S. L. C.; LIMA, A. O.; REGITANO, L. C. A.
Afiliação: | POLIANA FERNANDA GIACHETTO, CNPTIA; FERNANDA C. P. PEREIRA; FABIANA B. MOKRY; ROBERTO HIROSHI HIGA, CNPTIA; MAURICIO DE ALVARENGA MUDADU, CPPSE; MARCOS VINICIUS GUALBERTO B SILVA, CNPGL; SIMONE CRISTINA MEO NICIURA, CPPSE; FERNANDO FLORES CARDOSO, CPPSUL; MAURICIO MELLO DE ALENCAR, CPPSE; SARAH L. C. MEIRELLES, UFV; ANDRESSA O. LIMA, UFSCar; LUCIANA CORREIA DE ALMEIDA REGITANO, CPPSE.
Título: | Initial analysis of copy number variations in canchim beef cattle with extreme phenotypes for ribeye area.
Ano de publicação: | 2013
Fonte/Imprenta: | In: INTERNATIONAL PLANT & ANIMAL GENOME, 21., 2013, San Diego. [Abstracts...]. [S.l.: s.n.], 2013.
Páginas: | Não paginado.
Idioma: | Inglês
Notas: | Pôster P0572.
Conteúdo: | Genomic structural variation, in the form of large-scale insertions and deletions, as well as inversions and translocations, are referred to as copy number variations (CNVs). Compared to single nucleotide polymorphisms (SNPs), CNVs have potentially greater effects on gene structure, dosage and regulation, being an important source of phenotypic variation. In humans, CNVs are widespread in the genome and have been shown to be associated with complex traits. In livestock species, the characterization of this genetic variation is an important step toward linking genes or genomic regions with phenotypic traits of economic importance. Studies in cattle have revealed some CNVs associated with differences in host parasite resistance and breed-specific differences in adaptation, health, and production traits. We report initial data from an analysis of CNVs in Canchim, a synthetic cattle (5/8 Charolais + 3/8 Zebu) that has been selected for meat production in Brazil. Using the PennCNV software and data from 192 Canchim DNA samples with extreme phenotypes for ribeye area, genotyped with Illumina BovineHD BeadChip, a total of 6,985 CNVs were detected. The regions ranged from 20,012bp to 4,157,122bp, with mean and median of 140,484bp and 81,303bp, respectively. Copy number gains (62.09%) were found to be more common than deletions. Gene content of discovered CNVs and functional enrichment analysis are being assessed using Ensembl genes and cattle RefSeq databases, and PANTHER classification system, respectively. We expect to use these findings in genome wide association studies to better understand the genetic variation underlying meat quality in beef cattle.
Palavras-Chave: | Bioinformática; Copy number variations; Polimorfismo de nucleotídeo único; Single nucleotide polymorphisms.
Thesagro: | Variação Genética.
Thesaurus Nal: | Bioinformatics; Genetic variation; Single nucleotide polymorphism.
Categoria do assunto: | X Pesquisa, Tecnologia e Engenharia

URL:

http://ainfo.cnptia.embrapa.br/digital/bitstream/item/94588/1/P0572.odt
http://ainfo.cnptia.embrapa.br/digital/bitstream/item/97848/1/P0572.odt

Registro original: | Embrapa Agricultura Digital (CNPTIA)

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