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Genome-wide association study between copy number variation and feeding behavior, feed efficiency, and growth traits in Nellore cattle.
Benfica, Lorena F; Brito, Luiz F; do Bem, Ricardo D; Mulim, Henrique A; Glessner, Joseph; Braga, Larissa G; Gloria, Leonardo S; Cyrillo, Joslaine N S G; Bonilha, Sarah F M; Mercadante, Maria E Z.
Afiliação
  • Benfica LF; Department of Animal Sciences, Purdue University, 270 S. Russell Street, West Lafayette, IN, 47907, USA. lorenafbenfica@gmail.com.
  • Brito LF; Department of Animal Science, Faculty of Agricultural and Veterinary Sciences, Sao Paulo State University, Jaboticabal, SP, Brazil. lorenafbenfica@gmail.com.
  • do Bem RD; Department of Animal Sciences, Purdue University, 270 S. Russell Street, West Lafayette, IN, 47907, USA.
  • Mulim HA; Department of Animal Science, Faculty of Agricultural and Veterinary Sciences, Sao Paulo State University, Jaboticabal, SP, Brazil.
  • Glessner J; Department of Animal Sciences, Purdue University, 270 S. Russell Street, West Lafayette, IN, 47907, USA.
  • Braga LG; Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.
  • Gloria LS; Center for Applied Genomics, Children's Hospital of Philadelphia, Philadelphia, PA, USA.
  • Cyrillo JNSG; Department of Animal Science, Faculty of Agricultural and Veterinary Sciences, Sao Paulo State University, Jaboticabal, SP, Brazil.
  • Bonilha SFM; Department of Animal Sciences, Purdue University, 270 S. Russell Street, West Lafayette, IN, 47907, USA.
  • Mercadante MEZ; Institute of Animal Science, Sertaozinho, SP, Brazil.
BMC Genomics ; 25(1): 54, 2024 Jan 11.
Article em En | MEDLINE | ID: mdl-38212678
ABSTRACT

BACKGROUND:

Feeding costs represent the largest expenditures in beef production. Therefore, the animal efficiency in converting feed in high-quality protein for human consumption plays a major role in the environmental impact of the beef industry and in the beef producers' profitability. In this context, breeding animals for improved feed efficiency through genomic selection has been considered as a strategic practice in modern breeding programs around the world. Copy number variation (CNV) is a less-studied source of genetic variation that can contribute to phenotypic variability in complex traits. In this context, this study aimed to (1) identify CNV and CNV regions (CNVRs) in the genome of Nellore cattle (Bos taurus indicus); (2) assess potential associations between the identified CNVR and weaning weight (W210), body weight measured at the time of selection (WSel), average daily gain (ADG), dry matter intake (DMI), residual feed intake (RFI), time spent at the feed bunk (TF), and frequency of visits to the feed bunk (FF); and, (3) perform functional enrichment analyses of the significant CNVR identified for each of the traits evaluated.

RESULTS:

A total of 3,161 CNVs and 561 CNVRs ranging from 4,973 bp to 3,215,394 bp were identified. The CNVRs covered up to 99,221,894 bp (3.99%) of the Nellore autosomal genome. Seventeen CNVR were significantly associated with dry matter intake and feeding frequency (number of daily visits to the feed bunk). The functional annotation of the associated CNVRs revealed important candidate genes related to metabolism that may be associated with the phenotypic expression of the evaluated traits. Furthermore, Gene Ontology (GO) analyses revealed 19 enrichment processes associated with FF.

CONCLUSIONS:

A total of 3,161 CNVs and 561 CNVRs were identified and characterized in a Nellore cattle population. Various CNVRs were significantly associated with DMI and FF, indicating that CNVs play an important role in key biological pathways and in the phenotypic expression of feeding behavior and growth traits in Nellore cattle.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Estudo de Associação Genômica Ampla / Variações do Número de Cópias de DNA Tipo de estudo: Risk_factors_studies Limite: Animals / Humans Idioma: En Revista: BMC Genomics Assunto da revista: GENETICA Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Estudo de Associação Genômica Ampla / Variações do Número de Cópias de DNA Tipo de estudo: Risk_factors_studies Limite: Animals / Humans Idioma: En Revista: BMC Genomics Assunto da revista: GENETICA Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Estados Unidos