Tag-SNP selection using Bayesian genomewide association study for growth traits in Hereford and Braford cattle

被引:18
作者
Campos, Gabriel Soares [1 ]
Sollero, Bruna Pena [2 ]
Reiniann, Fernando Antonio [1 ]
Junqueira, Vinicius Silva [3 ]
Cardoso, Leandro Lunardini [1 ,2 ]
Yokoo, Marcos Jun Iti [2 ]
Boligon, Arione Augusti [1 ]
Braccini, Jose [4 ]
Cardoso, Fernando Flores [1 ,2 ]
机构
[1] Univ Fed Pelotas, Dept Zootecnia, BR-96010900 Pelotas, RS, Brazil
[2] Embrapa Pecuaria Sul, Bage, Brazil
[3] Univ Fed Vicosa, Dept Zootecnia, Vicosa, MG, Brazil
[4] Univ Fed Rio Grande do Sul, Dept Zootecnia, Porto Alegre, RS, Brazil
关键词
beef cattle; genomic prediction; GWAS; low-density panel; MEAT QUALITY TRAITS; WIDE ASSOCIATION; GENOMIC SELECTION; INTRAMUSCULAR FAT; CANDIDATE GENES; CARCASS; PREDICTION; HOLSTEIN; SCAN; INFORMATION;
D O I
10.1111/jbg.12458
中图分类号
S8 [畜牧、 动物医学、狩猎、蚕、蜂];
学科分类号
0905 ;
摘要
The aim of this study was to perform a Bayesian genomewide association study (GWAS) to identify genomic regions associated with growth traits in Hereford and Braford cattle, and to select Tag-SNPs to represent these regions in low-density panels useful for genomic predictions. In addition, we propose candidate genes through functional enrichment analysis associated with growth traits using Medical Subject Headings (MeSH). Phenotypic data from 126,290 animals and genotypes for 131 sires and 3,545 animals were used. The Tag-SNPs were selected with BayesB (pi = 0.995) method to compose low-density panels. The number of Tag-single nucleotide polymorphism (SNP) ranged between 79 and 103 SNP for the growth traits at weaning and between 78 and 100 SNP for the yearling growth traits. The average proportion of variance explained by Tag-SNP with BayesA was 0.29, 0.23, 0.32 and 0.19 for birthweight (BW), weaning weight (WW205), yearling weight (YW550) and postweaning gain (PWG345), respectively. For Tag-SNP with BayesA method accuracy values ranged from 0.13 to 0.30 for k-means and from 0.30 to 0.65 for random clustering of animals to compose reference and validation groups. Although genomic prediction accuracies were higher with the full marker panel, predictions with low-density panels retained on average 76% of the accuracy obtained with BayesB with full markers for growth traits. The MeSH analysis was able to translate genomic information providing biological meanings of more specific gene products related to the growth traits. The proposed Tag-SNP panels may be useful for future fine mapping studies and for lower-cost commercial genomic prediction applications.
引用
收藏
页码:449 / 467
页数:19
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