Data/hora: 16/06/2024 19:05:22

Biblioteca(s): 	Embrapa Agricultura Digital; Embrapa Gado de Leite; Embrapa Recursos Genéticos e Biotecnologia.	
Data corrente: 	19/05/2017	
Data da última atualização: 	30/12/2020	
Autoria: 	STAFUZZA, N. B.; ZERLOTINI NETO, A.; LOBO, F. P.; YAMAGISHI, M. E. B.; CHUD, T. C. S.; CAETANO, A. R.; MUNARI, D. P.; GARRICK, D. J.; MACHADO, M. A.; MARTINS, M. F.; CARVALHO, M. R.; COLE, J. B.; SILVA, M. V. G. B.	
Afiliação: 	NEDENIA BONVINO STAFUZZA, FCAV/Unesp; ADHEMAR ZERLOTINI NETO, CNPTIA; FRANCISCO PEREIRA LOBO, CNPTIA; MICHEL EDUARDO BELEZA YAMAGISHI, CNPTIA; TATIANE CRISTINA SELEGUIM CHUD, FCAV/Unesp; ALEXANDRE RODRIGUES CAETANO, Cenargen; DANÍSIO PRADO MUNARI, FCAV/Unesp; DORIAN J. GARRICK, Iowa State University; MARCO ANTONIO MACHADO, CNPGL; MARTA FONSECA MARTINS, CNPGL; MARIA RAQUEL CARVALHO, UFMG; JOHN BRUCE COLE, Agricultural Research Service; MARCOS VINICIUS GUALBERTO B SILVA, CNPGL.	
Título: 	Single nucleotide variants and InDels identified from whole-genome re-sequencing of Guzerat, Gyr, Girolando and Holstein cattle breeds.	
Ano de publicação: 	2017	
Fonte/Imprenta: 	Plos One, v. 12, n. 3, p. 1-15, 2017.	
DOI: 	https://doi.org/10.1371/journal.pone.0173954	
Idioma: 	Inglês	
Notas: 	Artigo e0173954. Na publicação: Adhemar Zerlotini, Marcos Vinicius Gualberto Barbosa da Silva.	
Conteúdo: 	Whole-genome re-sequencing, alignment and annotation analyses were undertaken for 12 sires representing four important cattle breeds in Brazil: Guzerat (multi-purpose), Gyr, Girolando and Holstein (dairy production). A total of approximately 4.3 billion reads from an Illumina HiSeq 2000 sequencer generated for each animal 10.7 to 16.4-fold genome coverage. A total of 27,441,279 single nucleotide variations (SNVs) and 3,828,041 insertions/deletions (InDels) were detected in the samples, of which 2,557,670 SNVs and 883,219 InDels were novel. The submission of these genetic variants to the dbSNP database significantly increased the number of known variants, particularly for the indicine genome. The concordance rate between genotypes obtained using the Bovine HD BeadChip array and the same variants identified by sequencing was about 99.05%. The annotation of variants identified numerous non-synonymous SNVs and frameshift InDels which could affect phenotypic variation. Functional enrichment analysis was performed and revealed that variants in the olfactory transduction pathway was over represented in all four cattle breeds, while the ECM-receptor interaction pathway was over represented in Girolando and Guzerat breeds, the ABC transporters pathway was over represented only in Holstein breed, and the metabolic pathways was over represented only in Gyr breed. The genetic variants discovered here provide a rich resource to help identify potential genomic markers and their associated molecular mechanisms that impact economically important traits for Gyr, Girolando, Guzerat and Holstein breeding programs.	
Palavras-Chave: 	Genetic variants; Genomic markers; Important traits; Molecular mechanisms; Polimorfismo de nucleotídeo único; Potential genomic markers; Raças bovinas; Single nucleotide variations.	
Thesagro: 	Gado; Variação genética.	
Thesaurus Nal: 	Cattle breeds; Genome; Single nucleotide polymorphism; Sires.	
Categoria do assunto: 	--
G Melhoramento Genético	
URL: 	http://ainfo.cnptia.embrapa.br/digital/bitstream/item/171980/1/AP-Single-nucleotide-Stafuzza-etal.pdf
http://ainfo.cnptia.embrapa.br/digital/bitstream/item/161515/1/Cnpgl-2017-PlosOne-Stafuzza-Single.pdf
http://ainfo.cnptia.embrapa.br/digital/bitstream/item/180929/1/journal.pone.0173954.pdf	
Registro original: 	Embrapa Agricultura Digital (CNPTIA)	
Exemplares: 	CENARGEN - (36823-1) - UPC - AP - DD -  -  -  - DIS
CNPGL - (23579-1) - UPC - AP - DD -  -  -  - DIS
CNPTIA - (19600-1) - UPC - AP - DD -  -  -  - DIS