Inclusion of cytoplasmic lineage effect and direct-maternal genetic covariance for genetic evaluation of growth traits in Nellore cattle

Autor(es)

Grigoletto, L. ; Mattos, E. C. ; Santana, M. H. A. ; Baldi, F. ; Eler, J. P. ; Ferraz, J. B. S.

• Tipo de documento: Artigo Científico
• Fonte: Genetics and Molecular Research; v. 15, n. 3 2016.
• Citações Web of Science: 0

Resumo

We evaluated the impact of cytoplasmic lineage effects (Lc) for growth traits on genetic evaluation, including the genetic covariance between direct and maternal effects (sigma(am)). Pedigree data from 496,190 Nellore animals and observations on birth weight (BW, N = 243,391), weaning weight (WW, N = 431,681), and post-weaning weight gain adjusted to 345 days (PWG, N = 172,131) were analyzed. Four univariate models were used to obtain estimates of (co) variance components using the restricted maximum likelihood method in the BLUPF90 program. Model 1 included Lc and sigma(am). Model 2 included Lc and sigma(am) was set to zero. Model 3 did not include Lc. Model 4 did not include Lc and sigma(am) was set to zero. These models considered the effects of the Lc as random. Phenotypic variance obtained through cytoplasmic lineage effects was determined for all traits, ranging from 0.07 to 0.15, 0.15 to 0.03, and 0.05 to 0.03% for BW, WW, and PWG, respectively, for models 1 and 2. Correlations between direct and maternal genetic components were positive for WW and negative for BW and PWG. No differences were observed for genetic parameter estimates or animal ranking with the inclusion of sigma(am). For BW, the likelihood ratio suggested that model 1 best fits the data, while model 4 was the most appropriate for WW and PWG. Thus, these models are recommended for genetic evaluations. Despite the low magnitude of cytoplasmic lineages, this effect could predict breeding value and improve the selection of animals for BW in this Nellore population. (AU)

• Processo FAPESP: 14/07566-2 - Genômica aplicada à produção de ruminantes
• Beneficiário: José Bento Sterman Ferraz
• Modalidade de apoio: Auxílio à Pesquisa - Temático