Predictive performance of genomic selection methods for carcass traits in Hanwoo beef cattle: impacts of the genetic architecture
Mehrban et al. Genet Sel Evol (2017) 49:1
DOI 10.1186/s12711-016-0283-0
Ge n e t i c s
Se l e c t i o n
Ev o l u t i o n
RESEARCH ARTICLE
Open Access
Predictive performance of genomic
selection methods for carcass traits in Hanwoo
beef cattle: impacts of the genetic architecture
Hossein Mehrban1, Deuk Hwan Lee2*, Mohammad Hossein Moradi3, Chung IlCho4, Masoumeh Naserkheil5
and Noelia Ibáñez‑Escriche6
Abstract
Background: Hanwoo beef is known for its marbled fat, tenderness, juiciness and characteristic flavor, as well as for
its low cholesterol and high omega 3 fatty acid contents. As yet, there has been no comprehensive investigation to
estimate genomic selection accuracy for carcass traits in Hanwoo cattle using dense markers. This study aimed at
evaluating the accuracy of alternative statistical methods that differed in assumptions about the underlying genetic
model for various carcass traits: backfat thickness (BT), carcass weight (CW), eye muscle area (EMA), and marbling
score (MS).
Methods: Accuracies of direct genomic breeding values (DGV) for carcass traits were estimated by applying fivefold
cross-validation to a dataset including 1183 animals and approximately 34,000 single nucleotide polymorphisms
(SNPs).
Results: Accuracies of BayesC, Bayesian LASSO (BayesL) and genomic best linear unbiased prediction (GBLUP) meth‑
ods were similar for BT, EMA and MS. However, for CW, DGV accuracy was 7% higher with BayesC than with BayesL
and GBLUP. The increased accuracy of BayesC, compared to GBLUP and BayesL, was maintained for CW, regardless
of the training sample size, but not for BT, EMA, and MS. Genome-wide association studies detected consistent large
effects for SNPs on chromosomes 6 and 14 for CW.
Conclusions: The predictive performance of the models depended on the trait analyzed. For CW, the results showed
a clear superiority of BayesC compared to GBLUP and BayesL. These findings indicate the importance of using a
proper variable selection method for genomic selection of traits and also suggest that the genetic architecture that
underlies CW differs from that of the other carcass traits analyzed. Thus, our study provides significant new insights
into the carcass traits of Hanwoo cattle.
Background
Hanwoo (Bos taurus coreanae) is an indigenous cattle
breed in Korea that has been intensively bred for meat
during the last 30 years [1]. Until the 1980s, Hanwoo cattle were used extensively for farming, transportation and
religious sacrifices [2] but they have now become popular for meat production owing to their rapid growth and
*Correspondence:
2
Department of Animal Life and Environment Science, Hankyong
National University, Jungang‑ro 327, Anseong‑si,
Gyeonggi‑do 456‑749, Korea
Full list of author information is available at the end of the article
high-quality meat. It is now one of the most economically
important species in Korea. The extensive marbling of
the Hanwoo beef is an important factor that influences
the perception of meat quality in commercial beef production [3]. Hanwoo beef is known for its marbled fat,
tenderness, juiciness and characteristic flavor. In addition, it has a lower cholesterol content and higher omega
3 fatty acid content, which makes it healthier than the
meat from other bovine breeds [4]. In spite of its high
price, i.e. almost three times that of imported beef meat
from other breeds [5], Hanwoo beef is very popular both
© The Author(s) 2017. This article is distributed under the terms of the Creative Commons Attribution 4.0 International License
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Mehrban et al. Genet Sel Evol (2017) 49:1
among Korean consumers and abroad because of these
invaluable traits [6].
The main aim of the Hanwoo beef industry is to
increase both the quality (marbling, tenderness and
flavor) and the quantity (carcass weight) of the meat.
Estimated breeding values for backfat thickness (BT),
carcass weight (CW), eye muscle area (EMA), and marbling score (MS) are commonly used as selection criteria in attempts to increase meat yield and quality, and
subsequently to improve the income generated from
steer feedlots and calf sales [7]. The recently developed
genomic selection approach is beginning to revolutionize
animal breeding. It refers to a genetic evaluation method
that uses phenotypic data and genotypes of dense single
nucleotide polymorphisms (SNPs) to estimate effects of
SNPs from a training population and subsequently to
predict the genetic values of selection candidates based
on their genotypes [8]. It has been widely applied to dairy
cattle breeding [9–11] and is now beginning to be used in
other livestock species [12, 13]. Genomic predictions for
beef cattle are attractive because many traits that affect
the profitability of beef production, such as carcass traits,
are difficult to select for because they are expensive to
measure or are measured only on the relatives of breeding bulls [14]. Accurate genomic estimated breeding
values would lead to greater genetic gain for these traits
[15].
Accuracy of genomic prediction is key to the success
of genomic selection [13]. Several analytical approaches
have been proposed to predict genetic values based on
genomic data, among which genomic (ridge regression)
best linear unbiased prediction (GBLUP or RRBLUP),
Bayesian shrinkage (e.g. BayesA) and variable selection models [e.g. BayesB, BayesCπ, BayesC and BayesL
(LASSO)] have been widely used [13, 16]. The main differences between these models are their assumptions
concerning the distributions of the effects of genetic
markers. GBLUP (or equivalent RRBLUP procedures)
models assume that all effects of SNPs are drawn from
the same normal distribution and thus, that all SNPs
have small effects [8]. The Bayesian approaches allow the
variances of the SNP effects to differ from one another.
However, Gianola et al. [17]. argued that for BayesA and
BayesB models there is a strong dependency on the prior
distributions of the marker variance because, in this case,
the posterior variance is estimated with only one marker,
thus its posterior distribution has only one more degree
of freedom than its prior distribution. BayesCπ, is less
sensitive to the prior assumption of the marker variance
compared with BayesA and BayesB models because all
SNPs have a common variance and the proportion of
SNPs with no effect (π) has a uniform prior distribution
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that is estimated during the analysis [18]. In BayesC,
π is considered to be a fixed value [19], which leads to
more accurate detection of qu (...truncated)