A genome-wide association study of meat and carcass traits in Australian cattle

被引:104
|
作者
Bolormaa, S. [1 ,2 ]
Neto, L. R. Porto [1 ,3 ]
Zhang, Y. D. [1 ,4 ,5 ]
Bunch, R. J. [1 ,3 ]
Harrison, B. E. [1 ,3 ]
Goddard, M. E. [1 ,2 ]
Barendse, W. [1 ,3 ]
机构
[1] Cooperat Res Ctr Beef Genet Technol, Armidale, NSW 2351, Australia
[2] Victorian Dept Primary Ind, Bundoora, Vic 3083, Australia
[3] Commonwealth Sci & Ind Res Org CSIRO Livestock In, Queensland Biosci Precinct, St Lucia, Qld 4067, Australia
[4] Univ New England, Armidale, NSW 2351, Australia
[5] NSW Dept Primary Ind, AGBU, Armidale, NSW 2351, Australia
关键词
cattle; DNA; fat; genome-wide association study; intramuscular; quantitative trait loci; selection; subcutaneous; SINGLE NUCLEOTIDE POLYMORPHISM; GROWTH-HORMONE RECEPTOR; ADAPTED BEEF BREEDS; QUALITY TRAITS; PHENOTYPIC CHARACTERIZATION; MILK-YIELD; TENDERNESS; LOCI; GENE; CALPASTATIN;
D O I
10.2527/jas.2010-3138
中图分类号
S8 [畜牧、 动物医学、狩猎、蚕、蜂];
学科分类号
0905 ;
摘要
Chromosomal regions containing DNA variation affecting the traits intramuscular fat percentage (IMF), meat tenderness measured as peak force to shear the LM (LLPF), and rump fat measured at the sacro-iliac crest in the chiller (CHILLP8) were identified using a set of 53,798 SNP genotyped on 940 taurine and indicine cattle sampled from a large progeny test experiment. Of these SNP, 87, 64, and 63 were significantly (P < 0.001) associated with the traits IMF, LLPF, and CHILLP8, respectively. A second, nonoverlapping sample of 1,338 taurine and indicine cattle from the same large progeny test experiment genotyped for 335 SNP, including as a positive control the calpastatin (CAST) c.2832A > G SNP, was used to confirm these locations. In total, 37 SNP were significantly (P < 0.05) associated with the same trait and with the same favorable homozygote in both data sets, representing 27 chromosomal regions. For the trait IMF, the effect of SNP in the confirmation data set was predicted from the discovery set by multiplying the estimated allele effect of each SNP in the discovery set by the number of copies of the reference allele of each SNP in the confirmation set. These weighted effects were then summed over all SNP to generate a molecular breeding value (MBV) for each animal in the confirmation data set. Using a bivariate analysis of MBV and IMF phenotypes of animals in the confirmation set, a panel of 14 SNP explained 5.6 and 15.6% of the phenotypic and genetic variance of IMF, respectively, in the confirmation data set. The amount of variation did not increase as more SNP were added to the MBV and instead decreased to 1.2 and 3.8% of the phenotypic and genetic variance of IMF, respectively, when 329 SNP were included in the analysis.
引用
收藏
页码:2297 / 2309
页数:13
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