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Genome-Wide Association Study Identifies Loci for Body Composition and Structural Soundness Traits in Pigs

  • Bin Fan,

    Affiliations Department of Animal Science and Center for Integrated Animal Genomics, Iowa State University, Ames, Iowa, United States of America, Key Laboratory of Agricultural Animal Genetics, Breeding and Reproduction, Ministry of Education & College of Animal Science and Technology, Huazhong Agricultural University, Wuhan, People's Republic of China

  • Suneel K. Onteru,

    Affiliation Department of Animal Science and Center for Integrated Animal Genomics, Iowa State University, Ames, Iowa, United States of America

  • Zhi-Qiang Du,

    Affiliation Department of Animal Science and Center for Integrated Animal Genomics, Iowa State University, Ames, Iowa, United States of America

  • Dorian J. Garrick,

    Affiliation Department of Animal Science and Center for Integrated Animal Genomics, Iowa State University, Ames, Iowa, United States of America

  • Kenneth J. Stalder,

    Affiliation Department of Animal Science and Center for Integrated Animal Genomics, Iowa State University, Ames, Iowa, United States of America

  • Max F. Rothschild

    mfrothsc@iastate.edu

    Affiliation Department of Animal Science and Center for Integrated Animal Genomics, Iowa State University, Ames, Iowa, United States of America

Genome-Wide Association Study Identifies Loci for Body Composition and Structural Soundness Traits in Pigs

  • Bin Fan, 
  • Suneel K. Onteru, 
  • Zhi-Qiang Du, 
  • Dorian J. Garrick, 
  • Kenneth J. Stalder, 
  • Max F. Rothschild
PLOS
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Abstract

Background

The recent completion of the swine genome sequencing project and development of a high density porcine SNP array has made genome-wide association (GWA) studies feasible in pigs.

Methodology/Principal Findings

Using Illumina's PorcineSNP60 BeadChip, we performed a pilot GWA study in 820 commercial female pigs phenotyped for backfat, loin muscle area, body conformation in addition to feet and leg (FL) structural soundness traits. A total of 51,385 SNPs were jointly fitted using Bayesian techniques as random effects in a mixture model that assumed a known large proportion (99.5%) of SNPs had zero effect. SNP annotations were implemented through the Sus scrofa Build 9 available from pig Ensembl. We discovered a number of candidate chromosomal regions, and some of them corresponded to QTL regions previously reported. We not only have identified some well-known candidate genes for the traits of interest, such as MC4R (for backfat) and IGF2 (for loin muscle area), but also obtained novel promising genes, including CHCHD3 (for backfat), BMP2 (for loin muscle area, body size and several FL structure traits), and some HOXA family genes (for overall leg action). The candidate regions responsible for body conformation and FL structure soundness did not overlap greatly which implied that these traits were controlled by different genes. Functional clustering analyses classified the genes into categories related to bone and cartilage development, muscle growth and development or the insulin pathway suggesting the traits are regulated by common pathways or gene networks that exert roles at different spatial and temporal stages.

Conclusions/Significance

This study is one of the earliest GWA reports on important quantitative traits in pigs, and the findings will contribute to the further biological function analysis of the identified candidate genes and potential utilization of them in marker assisted selection.

Introduction

The domestic pig has a long history of extensive natural and artificial selection partly to meet human dietary needs [1]. In the past, conventional artificial selection relying on phenotype and pedigree information has been practiced for genetic improvement. However, human population growth is increasing rapidly and nutritional input from animal industries will be required to feed a hungry world. Thus, to further increase the rate of genetic improvement, understanding of the interplay between polygenic and environmental factors controlling complex agriculturally important production and disease-resistance traits is needed [2]. This information could be integrated in marker-assisted selection (MAS) schemes to increase selection accuracy, shorten generation interval, and accelerate genetic improvement.

Both candidate gene and QTL mapping strategies have been used in domestic animals for the discovery of genetic markers suitable for MAS [3]. To date, more than 5,500 QTL relevant to ∼550 overlapping phenotypic traits have been deposited in pig QTLdb (http://www.animalgenome.org/cgi-bin/QTLdb/SS/index). However, those approaches have limitations. Candidate gene selection according to their putative physiological roles could be limited, and may miss novel gene identification and / or pathways influencing the traits. The regions of identified QTL are generally large and fine mapping is required to find more closely linked markers or causative variants suitable for marker-assisted selection. The consistency of QTL mapping may be limited when it is based among resource families developed from diverse founders [3]. However, the recently completed genome sequencing projects in many species and newly developed high density SNP arrays have made it possible to conduct GWA and genomic selection studies for several species of food producing animals, which has opened a new era for animal breeding [4][7].

In contrast to studies in humans where association analyses have the primary purpose of identifying markers for disease, the applications of dense SNP arrays in livestock focus on genomic selection (also termed genomic prediction or genomic evaluation), in order to improve selection accuracy to accelerate genetic improvement for economically important performance traits in breeding animals [8][10]. Assuming abundant availability of SNPs scattered throughout the genome which can capture linkage disequilibrium (LD) relationships with QTL, Meuwissen and colleagues [8] proposed a novel genomic selection concept, i.e., to predict an animal's breeding values using information provided by numerous SNPs across the entire genome. In this seminal work, two Bayesian approaches (Bayes A and Bayes B) were developed to predict genomic estimated breeding values (GEBV). In the years following this paper, alternative statistical approaches for genomic selection have been developed, derived from Bayesian models and some other parametric methods including GBLUP and mixed regression models [11][14]. This genomic selection methodology can be feasibly adapted for a GWA study and in the context of mixture models genomic regions and SNPs having high model frequency (i.e., frequently included in the model for GEBV prediction) can be identified as those likely linked to QTL [8], [13], [15].

Most of the published GWA studies carried out in animals involved Mendelian or disease related traits [16][20], although some evaluated single marker mixed model associations for growth traits [21], [22]. Few GWA studies using Bayesian methods that concurrently fit many or all SNPs have yet been reported.

Loin muscle depth or loin area and fat depth are good predictors of carcass lean content and are two traits targeted in pig breeding programs. Body conformation as well as feet and leg (FL) structural soundness are relevant to growth, feed intake capability, reproductive efficiency and sow longevity and are receiving more attention in modern swine production where pigs are being raised in confined production systems. It has been reported that approximately 40% of breeding sows were culled because of FL problems [23], [24]. The objective of this study was to perform a GWA study with the porcine 60K SNP BeadChip and to identify candidate SNPs/genes and chromosomal regions associated with growth, body composition, body conformation and FL structural traits, that might be suitable for MAS and genomic selection. To our knowledge, this is the first report from a GWA study on economically important production traits in pigs. Furthermore, it will contribute to a better understanding of the genetic control of complex animal agriculture traits.

Results

Phenotype statistics

Detailed descriptions of exploratory analyses of all phenotypes are in Tables S1 and S2. Apart from four traits in which the preferred value is intermediate, such as top line, weak/upright legs, front and rear legs turned in/out, population average values of body conformation and FL structure traits were between 2.19 and 5.39. The means for uneven front/rear toes were approximately 2.2, indicating small inside toe conformation was not a problem in the studied population. The number of animals with front/rear legs turned out was rare, so only traits for front/rear legs turned in were analyzed. Distribution analysis found that most of the traits apparently follow or nearly follow normal distributions (data not shown).

SNP chip data evaluation

The current Porcine 60K Beadchip has 64,232 SNPs [5], and based on the current pig genome annotation, Sus scrofa (SSC) Build 9, a total of 55,446 of these SNPs have been mapped to a genomic location. The average physical distance between any two neighboring SNPs on the same chromosome was approximately 41.6 Kb, ranging from 35.2 Kb (SSC14) to 81.4 Kb (SSCX) (Table S3). Based on the length of each chromosome in the USDA-MARC v2 (A) linkage map (http://www.thearkdb.org), the average genetic distance between SNPs on the chip is 0.046 cM, ranging from 0.02 cM (SSC1) to 0.08 cM (SSCX) (Table S3).

The distribution characteristics of SNPs were analyzed and among mapped loci, 15,338 are intragenic and are from 7,099 genes. The maximum number of SNPs from one gene is 33 and it is the PARK2 gene located between 6.5 and 7.5 Mb on SSC1.

Only five genotyped animals had average genotype call rates less than 80%, and were removed from further analysis. Additionally, SNPs with no call (1,886) or call rates less than 90% (400) were discarded. A total of 51,385 SNPs passed these quality control steps and were retained in the dataset.

GWA analysis

A population stratification analysis using IBS distance clustering showed that gilts from the two lines present in the data could be classified into one population, suggesting no significant genetic difference existed between these two lines. Since pedigree information indicated the lines had been separated, lines were fitted as a fixed effect in the model for association analyses.

Based on the heritability of each trait (Table S2), appropriate priors for the genetic and residual variances were obtained for input into the Bayesian statistical models. Results from the analyses including mean, posterior genetic and residual variances, and the resultant proportion of variation accounted for by SNPs are in Table S2. The genetic contribution to variation was relatively high for some traits for instance, 10th rib backfat with around 250 SNPs likely accounting for 54% of total genetic variance (µ = 0.995), loin muscle area with the same number of SNPs accounting for 55%. While other traits, such as weak top line and high top line, had relatively lower heritability estimates.

The putative candidate chromosomal regions were obtained by finding those genomic locations comprising windows of 5 consecutive SNPs with the highest genetic variance. Significance level was subsequently determined by bootstrap analyses under the null hypothesis that these windows did not harbor QTL. The model frequency statistic was used to find the most promising SNPs within these regions. With the assumption that the experiment had 50% power and a 99% null hypothesis of no QTL in the SNP window, then the PFP (proportion of false positives) from Fernando et al. [25] was 0.66 for p<0.01 and 0.16 for p<0.001. Therefore, we expected at least half of the reported QTL to be real for all the traits studied in the present work.

Analyses for two backfat traits, the last rib backfat and 10th rib backfat revealed that some of the genes underlying them were different, even though their genetic correlation has been estimated to be nearly 0.90 [26]. However, they did share several common regions, including those containing MC4R on SSC1, ATP6V1H and OPRK1 genes on SSC4, LDHD gene on SSC6, CHCHD3 gene on SSC18 and ATP2B3 genes on SSCX. In total, 21 regions were associated with last rib backfat (Figure S2), and genes in these regions are listed in Table S4.

As for 10th rib backfat, 18 candidate regions contributing the largest genetic variance were identified and they were distributed along chromosomes 1, 2, 4, 6, 7, 11, 12, 16, 18 and X (Figure 1). Surprisingly, one novel region was identified by the SNP ALGA0118164 on SSC18, with a high model frequency of 0.63, while others were under 0.25 (Figure S3). A larger population size will be required to verify the significance of this SNP since it represents a novel QTL region. Of these 18 peaks, 9 corresponded to QTL regions associated with 10th rib backfat in previous reports (Table S5). For example, the peak comprising four SNPs (INRA0004898, ALGA0006599, ALGA0006623 and ASGA0005017) on SSC1 was in a QTL region, where a known causative gene MC4R associated with fat and growth rate is located [27]. The peak pertaining SNP M1GA0005986 on SSC4 was close to a QTL region reported in the first pig QTL mapping study [28]. The genes within the regions were examined via pig Ensembl (http://www.ensembl.org/Sus_scrofa/Info/Index), and are listed in Table S5, together with those involved in fat development.

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Figure 1. Proportion of genetic variance explained by each window of 5 consecutive SNP markers across the genome for 10th rib backfat, which was used to determine the candidate genome regions surrounding the significant SNPs.

The X-axis is SNP marker position in genome order, and the Y-axis represents genetic variance of 5-SNP window (the exact candidate regions, the most promising SNPs and P values are shown in Table 1). Different colors represent SNPs on different chromosomes from SSC1 to X and unmapped markers.

https://doi.org/10.1371/journal.pone.0014726.g001

The SNP MC4R Asp298Asn along with any other SNP involved in previous patents or patent applications were not included in the chip so that no infringement would exist. However, the SNP MC4R Asp298Asn was evaluated in this population in an earlier study [29]. Genotypes of MC4R Asp298Asn were added to the dataset, and fitted as a random effect in a Bayes C model, achieving a model frequency of 0.08 (Figure 2a) with the average effect of allele A being 2.74E-03, implying allele A (Asn298) was associated with increased fat thickness, in agreement with Kim et al [27]. When MC4R Asp298Asn was fitted as a fixed effect, the model frequencies for other SNPs (INRA0004898, ALGA0006599, ALGA0006623 and ASGA0005017) dropped, suggesting there may be interactions associated with backfat between MC4R and other SNPs in the region.

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Figure 2. Haplotype analysis.

a) The haplotype blocks of the region between 165.47–168.63 Mb on SSC1 where four SNPs (INRA0004898, ALGA0006599, ALGA0006623 and ASGA0005017) with model frequency greater than 0.10 for 10th rib backfat and the MC4R gene (green color dot) were located , and b) The plots of model frequency for each haplotype containing the SNPs ALGA0006623 (underlined) and MC4R Asp298Asn (Italicized and underlined).

https://doi.org/10.1371/journal.pone.0014726.g002

Haplotype analysis was carried out on a 2.5 Mb region containing the MC4R Asp298Asn SNP and four other significant SNPs. The other SNPs were in different haplotype blocks, whereas ALGA0006623 and Asp298Asn were from the same block (Figure 2a). The five major haplotypes with occurrence frequency great than 1% were assigned to each individual and these covariates merged into the SNP dataset, and each haplotype model frequency was obtained (Figure 2b). Compared to that of single SNPs, the haplotype model frequency did not increase much. It suggested that there may be other genes associated with backfat besides MC4R in this region. Similar results have been reported previously [30], and further studies are needed to identify additional candidates.

Loin muscle area is related to muscle development, and 14 peaks were associated with this trait and the significance level of 13 of those candidate regions reached 0.05 (Figures 3 and S4). Eight of 14 peaks corresponded to previously reported QTL regions for LMA. The most significant SNP, INRA0052808 was within the BMP2 gene on SSC17, and the next two most significant SNPs, M1GA0002180 and M1GA0002244, were from the beginning of SSC2, where the IGF2 gene is located. Furthermore, in the region including ALGA0090171on SSC16, there were two potentially interesting genes, FST and NDUFS4 (Table S6).

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Figure 3. Proportion of genetic variance explained by each window of 5 consecutive SNP markers across the genome for 10th rib loin muscle area, which was used to determine the candidate genome regions surrounding the significant SNPs.

The X-axis is SNP marker position in genome order, and the Y-axis represents genetic variance of 5-SNP window (the exact candidate regions, the most promising SNPs and P values are shown in Table S6). Different colors represent SNPs on different chromosomes from SSC1 to X and unmapped markers.

https://doi.org/10.1371/journal.pone.0014726.g003

The genetic variance contributed by SNP windows were plotted against genomic location for body size (body length, depth and width) and body shape traits (correctness of top line, rib shape and hip structure) and are shown in Figures S6a-e, with genes from the candidate regions being listed in Table S7. There were a few common candidate regions over these body conformation traits. The BMP2 gene was associated with three body size traits, and interestingly, one allele was associated with long body length, shallow body and narrow body width (Table 1). The region at 270 Mb on SSC1 was also important for body size, where the PAPPA gene was considered as a candidate gene.

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Table 1. The SNPs within BMP2 genes associated with multiple traits, being estimated through a Bayesian procedure.

https://doi.org/10.1371/journal.pone.0014726.t001

For overall leg action, there were 14 candidate regions (Figures 4 and S5), which are from chromosomes 2, 3, 5, 6, 9, 13, 15, 16 and 18 (Table S8). The most significant region included SNPs H3GA0046827 and H3GA0046828 on SSC16, where no coding gene has been identified. In the candidate region on SSC2 surrounding MARC0022036, there was no gene with biological significance for skeletal development and locomotion. On SSC18, the region including HOX genes (HOXA1, HOXA2 and HOXA3) was identified, and on SSC9, the region containing the TWIST1 and SP4 genes was detected.

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Figure 4. Proportion of genetic variance explained by each window of 5 consecutive SNP markers across the genome for overall leg action, which was used to determine the candidate genome regions surrounding the significant SNPs.

The X-axis is SNP marker position in genome order, and the Y-axis represents genetic variance of 5-SNP window (the exact candidate regions, the most promising SNPs and P values are shown in Table S8). Different colors represent SNPs on different chromosomes from SSC1 to X and unmapped markers.

https://doi.org/10.1371/journal.pone.0014726.g004

However, for FL structural traits, which have relatively lower heritabilities, multiple genes seem to be involved. The putative candidate genes associated with traits were quite different, even for similar traits such as front leg pastern and rear leg pastern positions, and different traits at the same body position such as front leg pastern and front leg turned in (Figure S7 and Table S9). A clustering analysis for genes based on their functional annotation demonstrated that they could be classified into different categories, which related to the original traits. Some could be involved in bone and cartilage development such as SOX9, LRCH1, BMP2, COL4A3 and COL4A4, some might be related to muscle development such as MYOD1, MUSK, MYH1, MYH2, MYL9, MAP2K6 and MAP3K4, while others could be relevant to the insulin pathway such as PDX1, PTPN1, CTGFL and WISP2. These groups are all known to be associated with growth and development.

Discussion

The GWA and genomic selection studies conducted to date are beginning a promising era in animal breeding. To our knowledge, this might be the earliest GWA report on economically important growth and production traits in pigs. The primary results will contribute to the dissection of molecular mechanisms regulating important quantitative traits, identification of novel candidate genes and networks, and functional analysis of promising genes.

It is likely that GWA studies will be increasingly important to animal improvement. For disease related traits, a case-control strategy that is well-known in human studies has been generally utilized [16], [19]. For quantitative traits, several different methods have been explored [10], [18], [20]. In the present study a newly developed approach for GWA analyses between SNPs and quantitative traits was evaluated. In comparison to Bayes B, this approach was less reliant on priors for the genetic and residual variance, and computational time was reduced.

Population stratification is a confounding component that affects association analyses. The animals in this study were from two different genetic lines, which originated from the same breed resources. A clustering analysis based upon IBS distance classified them into one population. Nevertheless, the lines were fitted as a fixed effect in the model for association analyses based on pedigree information.

The Bayesian method used for association analyses in this study has been demonstrated to have higher accuracy even with different relationship scenarios between training and validation populations [31], [32]. It indicated that association results from the two lines in this study were robust and could be suitable for MAS and genomic selection in Large White and related pig populations.

A total of 18 candidate chromosomal regions were identified for 10th rib backfat, and half of them corresponded to previously reported QTL regions. The most promising SNP ALGA0118164 was 13 kb upstream of the CHCHD3 (coiled-coil-helix-coiled-coil-helix domain containing 3) gene, which is primarily expressed in mitochondria. The Leptin gene is around 4 Mb downstream of this gene, but the nearest SNP M1GA0023128 to Leptin was not in strong LD with ALGA0118164 and it did not achieve high model frequency (0.004). There are no reports about the association between CHCHD3 and phenotypes related to obesity/diabetes in humans and rodents. An investigation involving additional SNPs within CHCHD3 and functional analysis using adipocyte lines is warranted to verify the association of this gene with fat development.

One important region was identified between 165.47–168.63 Mb on SSC1, with around 20 coding genes annotated in Sus scrofa Build 9, including MC4R, one of the important functional genes associated with backfat. In pigs, the SNP Asp298Asn was found to be significantly associated with backfat and growth rate [27], and the association with fat has been implicated in pigs with diverse backgrounds. Four SNPs (INRA0004898, ALGA0006599, ALGA0006623 and ASGA0005017) distributed in different haplotype blocks were studied. The model frequency values decreased for the other SNPs when any one of them was considered as a fixed instead of random effect (data was not shown). The genes BCL2 and CCBE1 are two of interest. In addition, the candidate region harboring the SNP M1GA0005986 on SSC4 corresponded to a fat QTL location reported in the first porcine QTL mapping study [28]. Berg et al. [33] characterized this FAT1 QTL and refined its map position to a 3.3 cM interval between the RXRG and SDHC genes. These two genes are located at 89 Mb on SSC4 (Build 9), about 8 Mb from the region we found. The actual FAT1 QTL effects caused by the identified genes or others such as ATP6V1H and OPRK1 in this region should be explored to identify the causative mutation.

There were 14 candidate regions associated with LMA, and eight of them corresponded to QTL regions previously reported. The most interesting SNP INRA0052808 was from the BMP2 gene on SSC17. It is well known that BMP2 is involved in regulating early myogenesis and could inhibit proliferation or induce presumptive muscle cells to undergo apoptosis, thus inhibiting muscle development. These results, combined with those discussed later in this manuscript involving the association between BMP2 and body dimensions help explain the role this gene has in controlling body dimension and muscle development. A region on SSC2 including the significant SNPs M1GA0002180 and M1GA0002244 is close to the locus where the IGF2 gene is located. IGF2 has been considered to be one of the major causative genes associated with muscle development [34], and the G3072A mutation in intron 3 has been proposed to cancel in vitro interaction with a nuclear factor and was associated with a threefold increase in IGF2 messenger RNA expression in postnatal muscle [35].

A total of 14 candidate regions were found to be associated with overall leg action. On SSC18, one candidate region including a cluster of HOX family genes including HOXA1, HOXA2 and HOXA3 were identified. HOX genes encode a class of transcription factors that contain an antennapedia (HOM gene) related homeobox and are conserved throughout metazoan evolution in vertebrates, and they exert essential roles on the morphogenesis of skeletal structure along the antero-posterior axis [36]. On SSC6, a region including the FHL3 gene was associated with leg action. FHL3 negatively regulates myotube formation of C2C12 cells, and it could form a complex with MyoD inhibiting its transcription activity and control the expression of muscle specific genes such as muscle creatine kinase and myogenin [37]. Additionally, one region comprising three SNPs H3GA0027878, ALGA0054178 and ALGA0054186 on SSC9 was identified, and it contains the TWIST1 and SP4 genes, which are of interest for their association with leg action.

A number of candidate regions associated with body conformation traits were identified, but common genomic regions responsible for these traits appears to be rare. These results suggested that the genetic mechanisms underlying body growth and development are complicated, and the genes contributing to the body plan are in various networks and they might be regulated at different developmental stages, a fact known to biologists. The BMP2 gene was associated with all three body size traits. The allele T of SNP INRA0052808 located in BMP2 was associated with long body length, shallow body depth and narrow body width, and additionally it was associated with upright front/rear leg pastern postures and smaller LMA (Table 1). The genetic correlation between body length and body depth was positive while it was negative between these two traits and body width, and body width had a high favorable genetic correlation with LMA [26]. In practical breeding programs, animals could be selected as breeding stock based on the allele in BMP preferred by the breeder based on structural requirement.

There are a number of factors contributing to the FL structural soundness of livestock. The development of the body skeleton and muscle mass is an important factor determining body conformation, physical fitness and leg movement. In humans, the abnormal development of the skeleton can lead to a series of disorders, such as dwarfism, osteochondrosis, osteoporosis, osteopetrosis and osteoarthritis, which affect normal action capability and even result in lameness. Based on the functional clustering analyses we conducted, approximately 30% of candidate genes associated with FL could be classified into the categories of bone and cartilage development, skeletal muscle development and the insulin pathway. Some of the genes involved in bone and cartilage development were SOX9, LRCH1, FBN2, COL4A3, and COL4A4.

The genes and transcription factors MYOD1, MuSK, MYH1, MYH2, MYL9, MAP2K6 and MAP3K4 were found within candidate regions. Skeletal muscles are attached by tendons across joints, and muscle contraction drives the bones and joints. The muscle and skeleton function together and thus provide for animal movement as seen from a previous selection experiment [38], [39]. MYOD1 is involved in muscle differentiation and can induce fibroblasts to differentiate into myoblasts [40]. Mutations in the MuSK gene may cause congenital myasthenic syndromes (CMS), a type of hereditary disease characterized by muscles that fatigue easily resulting in muscle weakness caused by neuromuscular transmission dysfunction in humans [41]. MAP2K6 and MAP3K4 are two of the MAPK kinases that are involved in the p38 mitogen-activated protein kinase (MAPK) pathway. The p38 MAPKs regulate the transcriptional activities of MRFs and function in the remodeling of chromatin at specific muscle-regulatory regions, and it is one of the major intracellular signaling pathways affecting myogenesis [42].

Both insulin and IGF1 are known to induce a wide variety of growth and metabolic responses and play essential roles in anabolic regulation of bone metabolism [43]. Several genes involved in the insulin and IGF1 pathway were identified to be associated with the FL traits in this study. PDX1 could regulate the expression of pancreatic endocrine cell genes including insulin through the interaction at A-T rich regions contained within the promoter of these genes, and has a role in maintenance of the β-cell phenotype [44]. Mutations in the PTPN1 promoter might contribute to the development of T2D and related metabolic traits [45]. CTGFL could promote the adhesion of osteoblast cells and inhibit the binding of fibrinogen to integrin receptors, and may play important roles in modulating bone turnover [46]. Associations of these genes with FL soundness traits need to be further verified.

In this study, a number of candidate chromosomal regions relevant to the analyzed traits were identified, and some were consistent with previously reported QTL regions. These new SNP chip results demonstrated that combining dense SNP arrays and using the Bayes C approach is ideal for GWA studies on important quantitative traits in domestic animals. Meanwhile, some issues are worth discussing when the findings were compared with those of conventional candidate gene studies [29]. Several promising candidate genes such as PPARG, Leptin receptor (LEPR) and IGFBPs (for backfat deposition), Myogenic regulatory factors (MRFs) and Myostatin (MSTN) (for muscle growth), and CALCR, OXTR and PTHR (for leg related traits), were not found to be associated with the analyzed traits in these animals. In addition, most of the traits - associated SNPs (TASs) were from novel genes without obvious biological significance relevant to the analyzed traits, and most of TASs were located in the intergenic regions or introns of coding genes. Similarly, in GWA studies of the humans, the TASs have not always been from the putative candidate genes relevant to disorders or diseases [47]. It has been reported that 88% of TASs were intronic (45%) or intergenic (43%), 9% were nonsynonymous, 2% were in a 5′ or 3′ untranslated regulatory regions and 2% was synonymous [48]. In dairy cattle, the suggested candidate genes underlying Johne's disease such as SLC11A1, IL23R and NOD2 were not found to be associated with this disease [21]. In this study, we speculate that such discrepancies may have resulted from one of the following explanations: i) The TASs may be from genes that have not yet been annotated, or linked to the unmapped SNPs, therefore, further annotations on the current Sus scrofa Build 9 are necessary; ii) The sample size and the genetic backgrounds of the studied populations may have effects on association analyses, and additional pure breeds with larger sample size will be of help for GWA implications; iii) Although Bayesian methods are well suited for genomic selection and the statistics such as window variance and model frequency can be used to evaluate associations, the prediction accuracy of the methods were between 40–60%. Therefore, the indicator for association may not be the best one, and additional statistical approaches for GWA study are needed; iv) The large (∼40 Kb) average interval and uneven SNPs distributions of the current porcine 60 K BeadChip may be major limitations for haplotype blocks analyses and fine mapping [49], and a higher density SNP panel is worthy of being developed. Even with these limitations, the SNP chip and results presented here offer new opportunities to understanding the underlying genetic factors affecting these traits of interest.

Materials and Methods

Ethics statement

Animal care guidelines were followed according to the Institutional Animal Care and Use Committee (IACUC) at Iowa State University (Approval ID: log#7-05-5927-S).

Animals and traits

A total of 820 gilts were included in the study, which were commercial breeding stock sourced from Newsham Choice Genetics (West Des Moines, IA, USA) between October 2005 and July 2006. The gilts belonged to two genetic lines and included 412 Large White line pigs and 408 pigs from a Large White×Landrace cross.

Body composition and structural soundness evaluations were carried out on 14 dates, with females having an average body weight of 124±11 kg and age of 190±7 days at appraisal time. Body composition traits comprised ultrasonically measured loin muscle area at the 10th rib, 10th rib backfat and last rib backfat. Ultrasonic images were taken with a Pie Medical 200 (Classic Medical Supply, Inc., Tequesta, FL) by a single technician certified by the National Swine Improvement Federation. A total of 17 body structural soundness traits were recorded including body conformation (body length, depth and width, top line, rib shape and hip structure), front feet and leg structure (legs turned, buck knees, pastern posture, foot size and uneven toes), rear feet and leg structure (legs turned, weak/upright legs, pastern posture, foot size and uneven toes) and overall leg action, which is a general appraisal reflecting both structural soundness and freedom of other defects affecting the gait and locomotion. All of the structural soundness traits were independently evaluated by two experienced scorers using nine-point scales, where one and nine indicated the extreme phenotypes of the traits. The intermediate score is the most favorable for four of the scoring traits including top line, turned front legs, turned rear legs and weak/upright rear legs. Scoring criterions and the descriptions of scores are shown in Table S1 and Figure S1, respectively.

SNP array genotyping

A very small amount of ear tissue was collected from gilts using the TypiFixTM ear tag from Agrobiogen (Hilgertshausen, Germany). The DNA was isolated from dry ear tissue using the DNeasy 96 Blood & Tissue Kit (Qiagen, Valencia, CA, USA). DNA quantification was performed using a NanoDrop 1000 (Thermo Fisher Scientific Inc., Wilmington, DE, USA). DNA samples were submitted for genotyping with total DNA between 700–1000 ng, 260/280 ratio>1.50 and DNA concentration>20 ng/ul. The genotyping was done by GeneSeek Inc. (Lincoln, NE, USA) using the Porcine 60K BeadChip (Illumina, San Deigo, CA, USA) and approved standard techniques outlined by the manufacturer. Quality control (QC) was performed after we received the original SNP genotyping data. The SNPs were filtered with call rate≥80%, Gentrain Score≥50%, minor allele frequency (MAF)≥0.05 and P value of test for Hardy-Weinberg equilibrium≥1×E−6.

Phenotypic statistics

The statistical analyses for descriptive analyses including population mean and normal distribution testing were performed using the UNIVARIATE procedure of the SAS software package (SAS Institute, release 9.2, Cary, NC, USA). Top line, turned front leg, turned rear legs and weak/upright rear legs were each divided into two traits prior to analyses because of intermediate optimum of the original trait scoring (Table S2). In addition, these separated traits (such as high top line and weak top line, front legs turned in and front legs turned out) had different heritability and moderate negative genetic corrections [33], implying that they are influenced by different genetic factors.

Population stratification analysis

The animals in the study were from two genetic lines but originated from Large White or Large White×Landrace interbreed crossing. Population stratification was examined using an identical-by-state (IBS) distance clustering method in PLINK program [50].

Bayesian methods for GWA analyzes

A new Bayesian method for genomic selection (Bayes C) has been proposed [15], developed from the Bayes B and GBLUP approaches [8]. The Bayes B approach is sensitive to the assumed prior of the genetic variance, and accuracy of genomic prediction could be affected if that value was given incorrectly. However, Bayes C is more tolerant to prior genetic variance, and is described here as follows: where y is the vector of phenotypes of the analyzed traits, X is the incidence matrix for fixed effects, is the vector of fixed effects, K is the number of SNPs in the dataset, Zj is the column vector representing the SNP covariate at locus j, uj is the random substitution effect for locus j, which conditional on σ2u, is assumed normally distributed N(0, σ2u) when δj = 1, while uj = 0, when δj = 0, δj is a random 0/1 variable indicating the absence (with probability π) or presence (with probability 1−π) of locus j in the model, and e is the vector of random residual effects assumed normally distributed N(0, σ2e). Thus, both Bayes B and Bayes C are mixture models that assume a mixture of two distributions for the SNP effects, with assumed mixture fraction π. In these analyses, π was assumed to be 0.995. The variance σ2u (or σ2e) was a priori assumed to be scaled inverse chi-square with vu = 4 (or ve = 10) degree of freedom and scale parameters S2u (or S2e) [51]. Additionally, in Bayes C σ2u is common to all loci in the model in contrast to the locus specific variance component in Bayes B.

SNP effects uj were estimated using the Monte-Carlo means of the posterior distribution of these effects computed by a Gibbs sampling strategy. For a locus j, samples for δj were obtained from its conditional distribution given b, the effects at all other loci included in the model and the two variance components σ2u and σ2e. This conditional distribution can be written as where u-j is the vector of effects in the model other than at locus j. The f(y| b, u-j , σ2u, σ2e) was obtained as the sum of Pr(δj) f(y|δj, b, u-j, σ2u, σ2e) computed for δj  = 0 and for δj  = 1 [51].

In each iteration of a Monte Carlo Markov Chain, every SNP was subjected to a likelihood ratio test that determined the probability that SNP would be included in the model given the fixed effects and currently fitted markers, and that SNP was then included in the model in that iteration with the calculated probability. Evidence for an informative SNP was obtained by accumulating the frequency across iterations of the chain that a particular SNP was fitted in the model, we refer to this statistic as model frequency. If consecutive SNPs are in high linkage disequilibrium (LD) with the same QTL, then the effect of the QTL and the SNP model frequency will be distributed across all the SNPs in high LD with the QTL. For this reason model frequency of individual SNP is not a good indicator of the presence of QTL in genomic regions with high LD. Accordingly, two alternative approaches were used to infer presence of QTL. First, by accumulating the window model frequency whereby a genomic window of typically 5 immediately consecutive SNPs was counted as being included in the model when at least one of any of the SNPs in that window were in the model that iteration. Second, a QTL was inferred by computing a statistic representing the relative contribution of variation in window breeding value compared to variation in genomic breeding value. Window breeding value was computed by multiplying the number of Illumina B alleles that represent the SNP covariates for each consecutive SNP in a window by their respective posterior means for substitution effects. After computing these 5 SNP window breeding values for all animals in the population the variance of these breeding values was calculated. Windows that contributed the highest genetic variance were considered to be the strongest signals of association. Genomic breeding values are calculated using the same approach as window breeding values but utilized every SNP in the genome. These window approaches to identify important genomic regions accounted for linkage disequilibrium and better characterize QTL than individual SNP effects.

Several factors relevant to the traits, such as genetic line, measurement date and scorer, were considered as fixed class effects or covariates (e.g. body weight). The above procedures were implemented using a web-based program, GenSel (http://bigs.ansci.iastate.edu/bigsgui/login.html), developed by Fernando and Garrick [15].

Bootstrap analysis

The calculation of the genetic variance accounted for by a 5 SNP window accounts for linkage disequilibrium between the 5 neighboring SNPs and discriminates important chromosomal effects from spurious effects of single SNPs. The chromosomal regions or the clusters of SNPs in sliding windows with the greatest contributions are also most likely to be associated with the analyzed phenotypes, and are considered to represent the QTL at that location. Using a similar approach with high density SNP chip data, Sun et al [52] recently identified QTL with few false positives for a complex pedigree containing QTLMAS 2010 data. That study also reported that the present genomic approach is at least as successful as other competing methods to identify QTL.

The significance level of the putative candidate genomic regions was estimated using bootstrap analysis. Bootstrap samples were produced using the posterior means of the 53,815 SNPs to construct the distribution of the test statistic (genetic variance of a SNP window) for each putative QTL. A bootstrap sample of the vector y for replicate j () was created using the posterior means of the fixed and SNP effects, except that all those SNP contained in the window that formed the QTL were excluded, and a vector of simulated residuals were added, formed by sampling a vector of independent standard normal deviations, one deviation for each animal, scaled by the posterior mean of the residual standard deviation , according to:

These bootstrap samples are constructed according to the null hypothesis of no QTL in the identified SNP window. Each bootstrap sample was reanalyzed using the Bayes C model used for the real data, and the genetic variance of the SNP window corresponding to the QTL were accumulated across all the bootstrap samples, for comparison to the test statistic represented by the genetic variance of the SNP window identified in the analysis of the real data. If just 1 bootstrap statistic from the 1,000 simulated exceeded the test statistic from the real data, the comparison-wise p-value was determined to be 0.001<p<0.002. In addition, multiple testing was taken in to account using the probability of false positives (PFP) as in Fernando et al [25]. That approach controls the probability of false positive conclusions across all the tests undertaken, rather than the probability of making one mistake over all tests as would be the interpretation of an experiment-wise error correction.

Haplotype block and association analysis

Haplotype analysis was performed for the chromosomal regions where multiple candidate SNPs were located. The haplotype blocks were identified using Haploview (Ver 4.1) [53]. Haplotypes were obtained for each animal using the PHASE computer program (Ver. 2.1) [54], and for each individual, it carried 0, 1 and/or 2 copies of a certain haplotype. The association between the haplotypes and the traits were estimated using GenSel [15] as described above.

Gene ontology

For regions harboring the SNP with the highest model frequency, gene search was performed via Sus Scrofa Build 9 of pig Ensembl (http://www.ensembl.org/Sus_scrofa/Info/Index). The QTL location for relevant traits and the physical positions of microsatellite markers retrieved from ArkDB (http://www.thearkdb.org) and PigQTL (http://www.animalgenome.org/cgi-bin/QTLdb/SS/index) were integrated, to obtain connections between QTL and candidate regions found from GWA studies.

Gene ontology analysis was performed to extract the functional annotation clustering using an online site called DAVID (http://david.abcc.ncifcrf.gov).

In addition, for those SNPs with high model frequency that were unassigned to any genomic location, their joint LD with SNPs of known location was calculated using r2 so that the possible physical positions could be deduced from the SNPs with known location that had the highest estimated r2 with the unassigned SNP.

Supporting Information

Figure S1.

The scoring criteria for body conformation, and feet and leg structure soundness traits.

https://doi.org/10.1371/journal.pone.0014726.s001

(0.10 MB TIF)

Figure S2.

Proportion of genetic variance explained by each window of 5 consecutive SNP markers across the genome for last rib backfat, which was used to determine the candidate genome regions surrounding the significant SNPs. The X-axis is SNP marker position in genome order, and the Y-axis represents accumulative genetic variance of 5-SNP window (the exact candidate regions, the most promising SNPs and P values are shown in Table S4). Different colors represent SNPs on different chromosomes from SSC1 to X and unmapped markers.

https://doi.org/10.1371/journal.pone.0014726.s002

(0.07 MB TIF)

Figure S3.

The SNP model frequency plots for assessing associations between markers and 10th rib backfat. The X-axis is SNP marker position in genome order, and the Y-axis represents model frequency (0.10 was considered as threshold for 10th rib back fat here). Different colors represent SNPs on different chromosomes from SSC1 to X and unmapped markers.

https://doi.org/10.1371/journal.pone.0014726.s003

(0.08 MB TIF)

Figure S4.

The plots of model frequency of SNPs for assessing the associations between the markers and 10th rib loin muscle area. The X-axis is SNP marker position in genome order, and the Y-axis represents model frequency (0.10 was considered as threshold for 10th rib loin muscle area here). Different colors represent SNPs on different chromosomes from SSC1 to X and unmapped markers.

https://doi.org/10.1371/journal.pone.0014726.s004

(0.10 MB TIF)

Figure S5.

The plots of model frequency of SNPs for assessing the associations between the markers and overall leg action. The X-axis is SNP marker position in genome order, and the Y-axis represents model frequency (0.05 was considered as threshold for overall leg action). Different colors represent SNPs on different chromosomes from SSC1 to X and unmapped markers.

https://doi.org/10.1371/journal.pone.0014726.s005

(0.10 MB TIF)

Figure S6.

Proportion of genetic variance explained by each window of 5 SNP consecutive markers across the genome for body conformation traits, which was used to determine the candidate genome regions surrounding the significant SNPs. The body conformation traits are a) body length; b) body depth; c) body width; d) rib shape and e) Hip structure. The X-axis is SNP marker position in genome order, and the Y-axis represents accumulative genetic variance of 5-SNP window (the exact candidate regions, the most promising SNPs and P values are shown in Table S7). Different colors represent SNPs on different chromosomes from SSC1 to X and unmapped markers.

https://doi.org/10.1371/journal.pone.0014726.s006

(1.65 MB TIF)

Figure S7.

Proportion of genetic variance explained by each window of 5 consecutive SNP markers across the genome for feet and leg structure soundness traits, which was used to determine the candidate genome regions surrounding the significant SNPs. The feet and leg structure soundness traits are a) front leg pastern; b) rear leg pastern; c) front buck knee; d) front feet size; e) rear feet size; f) front uneven toes and g) rear uneven toes. The X-axis is SNP marker position in genome order, and the Y-axis represents accumulative genetic variance of 5-SNP window (the exact candidate regions, the most promising SNPs and P values are shown in Table S9). Different colors represent SNPs on different chromosomes from SSC1 to X and unmapped markers.

https://doi.org/10.1371/journal.pone.0014726.s007

(2.15 MB TIF)

Table S1.

The description of the 17 analyzed traits of body conformation, feet and leg structure and overall leg action.

https://doi.org/10.1371/journal.pone.0014726.s008

(0.04 MB DOC)

Table S2.

The overall statistics about population means, estimated heritability and the genetic parameters of Bayes C analyses for the traits.

https://doi.org/10.1371/journal.pone.0014726.s009

(0.05 MB DOC)

Table S3.

The overall statistics on average interval between SNPs and SNP distribution of porcine 60K SNP array.

https://doi.org/10.1371/journal.pone.0014726.s010

(0.05 MB DOC)

Table S4.

The detail information about candidate regions and the most significant SNPs associated with last rib backfat.

https://doi.org/10.1371/journal.pone.0014726.s011

(0.05 MB DOC)

Table S5.

The detail information about the putative candidate regions and the most significant SNPs associated with 10th rib backfat.

https://doi.org/10.1371/journal.pone.0014726.s012

(0.05 MB DOC)

Table S6.

The detail information about the putative candidate regions and the most significant SNPs associated with 10th rib loin muscle area.

https://doi.org/10.1371/journal.pone.0014726.s013

(0.05 MB DOC)

Table S7.

The detail information about candidate regions and the most significant SNPs associated with body conformation traits.

https://doi.org/10.1371/journal.pone.0014726.s014

(0.09 MB DOC)

Table S8.

The detail information about the putative candidate regions and the most significant SNPs associated with overall leg action.

https://doi.org/10.1371/journal.pone.0014726.s015

(0.05 MB DOC)

Table S9.

The detail information about candidate regions and the most significant SNPs associated with feet and leg structural soundness traits.

https://doi.org/10.1371/journal.pone.0014726.s016

(0.19 MB DOC)

Acknowledgments

The authors thank Drs. Jack Dekkers and Rohan Fernando for valuable suggestions on data analyses, and thank Drs. Zhiliang Hu and Tinghua Huang for help with SNP chip annotations. The efforts of Drs. Benny Mote, Timo Serenius and Marja Nikkilä in trait scoring and data recording are appreciated.

Author Contributions

Conceived and designed the experiments: BF KS MR. Performed the experiments: BF SKO MR. Analyzed the data: BF ZQD DG MR. Contributed reagents/materials/analysis tools: DG KS. Wrote the paper: BF ZQD KS MR.

References

  1. 1. Albarella U, Dobney K, Ervynck A, Rowley-Conwy P (2007) Pigs and Human: 10,000 years of interaction. New York: Oxford University Press Inc. 11 p.U. AlbarellaK. DobneyA. ErvynckP. Rowley-Conwy2007Pigs and Human: 10,000 years of interaction.New YorkOxford University Press Inc11
  2. 2. Andersson L, Georges M (2004) Domestic-animal genomics: Deciphering the genetics of complex traits. Nat Rev Genet 5: 202–212.L. AnderssonM. Georges2004Domestic-animal genomics: Deciphering the genetics of complex traits.Nat Rev Genet5202212
  3. 3. Rothschild MF, Hu ZL, Jiang ZH (2007) Advances in QTL mapping in pigs. Int J Biol Sci 3: 192–197.MF RothschildZL HuZH Jiang2007Advances in QTL mapping in pigs.Int J Biol Sci3192197
  4. 4. Matukumalli LK, Lawley CT, Schnabel RD, Taylor JF, Allan MF, et al. (2009) Development and Characterization of a High Density SNP Genotyping Assay for Cattle. PLoS One 4: e5350.LK MatukumalliCT LawleyRD SchnabelJF TaylorMF Allan2009Development and Characterization of a High Density SNP Genotyping Assay for Cattle.PLoS One4e5350
  5. 5. Ramos AM, Crooijmans RPMA, Affara NA, Amaral AJ, Archibald AL, et al. (2009) Design of a high density SNP genotyping assay in the pig using SNPs identified and characterized by next generation sequencing technology. PLoS One. 4: e6524.AM RamosRPMA CrooijmansNA AffaraAJ AmaralAL Archibald2009Design of a high density SNP genotyping assay in the pig using SNPs identified and characterized by next generation sequencing technology.PLoS One.4e6524
  6. 6. Elsik CG, Tellam RL, Worley KC, Gibbs RA, et al. The Bovine Genome Sequencing and Analysis Consortium (2009) The genome sequence of taurine cattle: a window to ruminant biology and evolution. Science 324: 522–528.CG ElsikRL TellamKC WorleyRA GibbsThe Bovine Genome Sequencing and Analysis Consortium2009The genome sequence of taurine cattle: a window to ruminant biology and evolution.Science324522528
  7. 7. Wade CM, Giulotto E, Sigurdsson S, Zoli M, Gnerre S, et al. (2009) Genome sequence, comparative analysis, and population genetics of the domestic horse. Science 326: 865–867.CM WadeE. GiulottoS. SigurdssonM. ZoliS. Gnerre2009Genome sequence, comparative analysis, and population genetics of the domestic horse.Science326865867
  8. 8. Meuwissen THE, Hayes BJ, Goddard ME (2001) Prediction of total genetic value using genome-wide dense marker maps. Genetics 157: 1819–1829.THE MeuwissenBJ HayesME Goddard2001Prediction of total genetic value using genome-wide dense marker maps.Genetics15718191829
  9. 9. Goddard ME, Hayes BJ (2009) Mapping genes for complex traits in domestic animals and their use in breeding programmes. Nat Rev Genet 10: 381–391.ME GoddardBJ Hayes2009Mapping genes for complex traits in domestic animals and their use in breeding programmes.Nat Rev Genet10381391
  10. 10. Hayes BJ, Bowman PJ, Chamberlain AJ, Goddard ME (2009) Genomic selection in dairy cattle: Progress and challenges. J Dairy Sci. 92: 433–443.BJ HayesPJ BowmanAJ ChamberlainME Goddard2009Genomic selection in dairy cattle: Progress and challenges.J Dairy Sci.92433443
  11. 11. Gianola D, Fernando RL, Stella A (2006) Genomic-assisted prediction of genetic value with semiparametric procedures. Genetics 173: 1761–1776.D. GianolaRL FernandoA. Stella2006Genomic-assisted prediction of genetic value with semiparametric procedures.Genetics17317611776
  12. 12. Aulchenko YS, de Koning DJ, Haley C (2007) Genomewide rapid association using mixed model and regression: a fast and simple method for genomewide pedigree-based quantitative trait loci association analysis. Genetics 177: 577–585.YS AulchenkoDJ de KoningC. Haley2007Genomewide rapid association using mixed model and regression: a fast and simple method for genomewide pedigree-based quantitative trait loci association analysis.Genetics177577585
  13. 13. Verbyla KL, Hayes BJ, Bowman PJ, Goddard ME (2009) Accuracy of genomic selection using stochastic variable selection in Australian Holstein Friesian dairy cattle. Genet Res Camb 91: 307–311.KL VerbylaBJ HayesPJ BowmanME Goddard2009Accuracy of genomic selection using stochastic variable selection in Australian Holstein Friesian dairy cattle.Genet Res Camb91307311
  14. 14. Calus MPL (2010) Genomic breeding value prediction: methods and procedures. Animal. 4: 157–164.MPL Calus2010Genomic breeding value prediction: methods and procedures. Animal.4157164
  15. 15. Fernando RL, Garrick DJ (2008) GenSel - User manual for a portfolio of genomic selection related analyses. RL FernandoDJ Garrick2008GenSel - User manual for a portfolio of genomic selection related analyses.Animal Breeding and Genetics, Iowa State University, Ames. http://bigs.ansci.iastate.edu/bigsgui/login.html. Animal Breeding and Genetics, Iowa State University, Ames. http://bigs.ansci.iastate.edu/bigsgui/login.html.
  16. 16. Karlsson EK, Baranowska I, Wade CM, Hillbertz NS, Zody MC, et al. (2007) Efficient mapping of mendelian traits in dogs through genome-wide association. Nat Genet 39: 1321–1328.EK KarlssonI. BaranowskaCM WadeNS HillbertzMC Zody2007Efficient mapping of mendelian traits in dogs through genome-wide association.Nat Genet3913211328
  17. 17. Feugang JM, Kaya A, Page GP, Chen L, Mehta T, et al. (2009) Two-stage genome-wide association study identifies integrin beta 5 as having potential role in bull fertility. BMC Genomics 10: 176.JM FeugangA. KayaGP PageL. ChenT. Mehta2009Two-stage genome-wide association study identifies integrin beta 5 as having potential role in bull fertility.BMC Genomics10176
  18. 18. Hayes BJ, Bowman PJ, Chamberlain AJ, Savin K, Van Tassell CP, et al. (2009) A validated genome wide association study to breed cattle adapted to an environment altered by climate change. PLoS One 4: e6676.BJ HayesPJ BowmanAJ ChamberlainK. SavinCP Van Tassell2009A validated genome wide association study to breed cattle adapted to an environment altered by climate change.PLoS One4e6676
  19. 19. Wood SH, Ke XY, Nuttall T, McEwan N, Ollier WE, et al. (2009) Genome-wide association analysis of canine atopic dermatitis and identification of disease related SNPs. Immunogenetics 61: 765–772.SH WoodXY KeT. NuttallN. McEwanWE Ollier2009Genome-wide association analysis of canine atopic dermatitis and identification of disease related SNPs.Immunogenetics61765772
  20. 20. Settles M, Zanella R, McKay SD, Schnabel RD, Taylor JF, et al. (2009) A whole genome association analysis identifies loci associated with Mycobacterium avium subsp. paratuberculosis infection status in US Holstein cattle. Anim Genet 40: 655–662.M. SettlesR. ZanellaSD McKayRD SchnabelJF Taylor2009A whole genome association analysis identifies loci associated with Mycobacterium avium subsp. paratuberculosis infection status in US Holstein cattle.Anim Genet40655662
  21. 21. Snelling WM, Allan MF, Keele JW, Juehn LA, McDanel T, et al. (2010) Genome-wide association study of growth in crosbred beef cattle. J Anim Sci. WM SnellingMF AllanJW KeeleLA JuehnT. McDanel2010Genome-wide association study of growth in crosbred beef cattle.J Anim SciIn Press.
  22. 22. Abasht B, Sandford E, Arango J, Settar P, Fulton JE, et al. (2009) Extent and consistency of linkage disequilibrium and identification of DNA markers for production and egg quality traits in commercial layer chicken populations. BMC Genomics 10: Suppl 2S2.B. AbashtE. SandfordJ. ArangoP. SettarJE Fulton2009Extent and consistency of linkage disequilibrium and identification of DNA markers for production and egg quality traits in commercial layer chicken populations.BMC Genomics10Suppl 2S2
  23. 23. Stalder KJ, Knauer M, Baas TJ, Rothschild MF, Mabry JW (2004) Sow longevity. Pig News and Information 25: 53N–74N.KJ StalderM. KnauerTJ BaasMF RothschildJW Mabry2004Sow longevity.Pig News and Information2553N74N
  24. 24. Kirk RK, Svensmark B, Ellegarrd LP, Jensen HE (2005) Locomotive disorders associated with sow mortality in Danish pig herds. J Vet Med A 52: 423–428.RK KirkB. SvensmarkLP EllegarrdHE Jensen2005Locomotive disorders associated with sow mortality in Danish pig herds.J Vet Med A52423428
  25. 25. Fernando RL, Nettleton D, Southey BR, Dekkers JCM, Rothschild MF, Soller M (2004) Controlling the proportion of false positives in multiple dependent tests. Genetics 166: 611–619.RL FernandoD. NettletonBR SoutheyJCM DekkersMF RothschildM. Soller2004Controlling the proportion of false positives in multiple dependent tests.Genetics166611619
  26. 26. Nikkilä M, Stalder K, Mote B, Lampe J, Thorn B, et al. (2008) Heritabilities and genetic correlations of body composition and structural soundness traits in commercial gilts. M. NikkiläK. StalderB. MoteJ. LampeB. Thorn2008Heritabilities and genetic correlations of body composition and structural soundness traits in commercial gilts.Iowa State University Animal Industry Report 2008. A.S. Leaflet R2349. http:www.ans.iastate.edu/report/air. Iowa State University Animal Industry Report 2008. A.S. Leaflet R2349. http:www.ans.iastate.edu/report/air.
  27. 27. Kim KS, Larsen N, Short T, Plastow G, Rothschild MF (2000) A missense variant of the porcine melanocortin-4 receptor (MC4R) gene is associated with fatness, growth, and feed intake traits. Mamm Genome 11: 131–135.KS KimN. LarsenT. ShortG. PlastowMF Rothschild2000A missense variant of the porcine melanocortin-4 receptor (MC4R) gene is associated with fatness, growth, and feed intake traits.Mamm Genome11131135
  28. 28. Andersson L, Haley CS, Ellegren H, Knott SA, Johansson M, et al. (1994) Genetic mapping of quantitative trait loci for growth and fatness in pigs. Science 263: 1771–1774.L. AnderssonCS HaleyH. EllegrenSA KnottM. Johansson1994Genetic mapping of quantitative trait loci for growth and fatness in pigs.Science26317711774
  29. 29. Fan B, Onteru , SK , Mote B, Serenius T, Stalder KJ, et al. (2009) Large-scale association study for structural soundness and leg locomotion traits in the pig. Genet Sel Evol 41: 14.B. FanOnteruSKB. MoteT. SereniusKJ Stalder2009Large-scale association study for structural soundness and leg locomotion traits in the pig.Genet Sel Evol4114
  30. 30. Park HB, Carlborg Ö, Marklund S, Andersson S (2002) Melanocortin-4 receptor (MC4R) genotypes have no major effect on fatness in a Large White × Wild Boar intercross. Anim Genet 33: 155–157.HB ParkÖ. CarlborgS. MarklundS. Andersson2002Melanocortin-4 receptor (MC4R) genotypes have no major effect on fatness in a Large White × Wild Boar intercross.Anim Genet33155157
  31. 31. Ibanez-Escriche N, Fernando RL, Toosi A, Dekkers JC (2009) Genomic selection of purebred for crossbred performance. Genet Sel Evol 41: 12.N. Ibanez-EscricheRL FernandoA. ToosiJC Dekkers2009Genomic selection of purebred for crossbred performance.Genet Sel Evol4112
  32. 32. Toosi A, Fernando RL, Dekkers JCM (2010) Genomic selection in admixed and crossbred populations. J Anim Sci 88: 32–46.A. ToosiRL FernandoJCM Dekkers2010Genomic selection in admixed and crossbred populations.J Anim Sci883246
  33. 33. Berg F, Stern S, Andersson K, Andersson L, Moller M (2006) Refined localization of the FAT1 quantitative trait locus on pig chromosome 4 by marker-assisted backcrossing. BMC Genetics 7: 17.F. BergS. SternK. AnderssonL. AnderssonM. Moller2006Refined localization of the FAT1 quantitative trait locus on pig chromosome 4 by marker-assisted backcrossing.BMC Genetics717
  34. 34. Jeon JT, Carlborg O, Törnsten A, Giuffra E, Amarger V, et al. (1999) A paternally expressed QTL affecting skeletal and cardiac muscle mass in pigs maps to the IGF2 locus. Nat Genet 21: 157–158.JT JeonO. CarlborgA. TörnstenE. GiuffraV. Amarger1999A paternally expressed QTL affecting skeletal and cardiac muscle mass in pigs maps to the IGF2 locus.Nat Genet21157158
  35. 35. Van Laere AS, Nguyen M, Braunschweig M, Nezer C, Collette C, et al. (2003) A regulatory mutation in IGF2 causes a major QTL effect on muscle growth in the pig. Nature 425: 832–836.AS Van LaereM. NguyenM. BraunschweigC. NezerC. Collette2003A regulatory mutation in IGF2 causes a major QTL effect on muscle growth in the pig.Nature425832836
  36. 36. Favier B, Dollé P (1997) Developmental functions of mammalian Hox genes. Mol Human Rep 3: 115–131.B. FavierP. Dollé1997Developmental functions of mammalian Hox genes.Mol Human Rep3115131
  37. 37. Cottle DL, McGrath MJ, Cowling BS, Coghill ID, Brown SB, et al. (2007) FHL3 binds MyoD and negatively regulates myotube formation. J Cell Sci 120: 1423–1435.DL CottleMJ McGrathBS CowlingID CoghillSB Brown2007FHL3 binds MyoD and negatively regulates myotube formation.J Cell Sci12014231435
  38. 38. Draper DD, Rothschild MF, Christian LL (1991) Effects of divergent selection for leg weakness on bone and muscle cross sectional areas in Duroc swine. Am J Vet Res 52: 164–168.DD DraperMF RothschildLL Christian1991Effects of divergent selection for leg weakness on bone and muscle cross sectional areas in Duroc swine.Am J Vet Res52164168
  39. 39. Draper DD, Rothschild MF, Christian LL (1992) Effects of divergent selection for leg weakness on muscle and bone characteristics in Duroc swine. Genet Sel Evol 24: 363–374.DD DraperMF RothschildLL Christian1992Effects of divergent selection for leg weakness on muscle and bone characteristics in Duroc swine.Genet Sel Evol24363374
  40. 40. Dayton WR, White ME (2008) Cellular and molecular regulation of muscle growth and development in meat animals. J Anim Sci 86: E217–E225.WR DaytonME White2008Cellular and molecular regulation of muscle growth and development in meat animals.J Anim Sci86E217E225
  41. 41. Kim CH, Xiong WC, L Mei (2005) Inhibition of Musk expression by CREB interacting with a CRE-like element and Myod. Mol Cell Bio 25: 5329–5338.CH KimWC XiongMei L2005Inhibition of Musk expression by CREB interacting with a CRE-like element and Myod.Mol Cell Bio2553295338
  42. 42. Keren A, Tamir Y, Bengal E (2006) The p38 MAPK signaling pathway: A major regulator of skeletal muscle development. Mol Cell Endocrinol 252: 224–230.A. KerenY. TamirE. Bengal2006The p38 MAPK signaling pathway: A major regulator of skeletal muscle development.Mol Cell Endocrinol252224230
  43. 43. Verhaeghe J, Bouillon R (2002) Effects of Diabetes and Insulin on bone metabolism. In: Bilezikian JP, Raisz L, Rodan GA, editors. Principles of Bone Biology (2nd Edition). San Diego: Academic Press. pp. 549–562.J. VerhaegheR. Bouillon2002Effects of Diabetes and Insulin on bone metabolism.JP BilezikianL. RaiszGA RodanPrinciples of Bone Biology (2nd Edition)San DiegoAcademic Press549562
  44. 44. Qian J, Kaytor EN, Towle HC, Olson I (1999) Upstream stimulatory factor regulates Pdx-1 gene expression in differentiated pancreatic b-cells. Biochem J 341: 315–322.J. QianEN KaytorHC TowleI. Olson1999Upstream stimulatory factor regulates Pdx-1 gene expression in differentiated pancreatic b-cells.Biochem J341315322
  45. 45. Meshkani R, Taghikhani M, Al-Kateb H, Larijani B, Khatami S, et al. (2007) Polymorphisms within the protein Tyrosine Phosphatase 1B (PTPN1) gene promoter: Functional characterization and association with type 2 Diabetes and related metabolic traits. Clin Chem 53: 1585–1592.R. MeshkaniM. TaghikhaniH. Al-KatebB. LarijaniS. Khatami2007Polymorphisms within the protein Tyrosine Phosphatase 1B (PTPN1) gene promoter: Functional characterization and association with type 2 Diabetes and related metabolic traits.Clin Chem5315851592
  46. 46. Nakanishi T, Yamaai T, Asano M, Nawachi K, Suzuki M, et al. (2001) Overexpression of connective tissue growth factor/hypertrophic chondrocyte-specific gene product 24 decreases bone density in adult mice and induces dwarfism. Biochem Biophys Res Commun 281: 678–681.T. NakanishiT. YamaaiM. AsanoK. NawachiM. Suzuki2001Overexpression of connective tissue growth factor/hypertrophic chondrocyte-specific gene product 24 decreases bone density in adult mice and induces dwarfism.Biochem Biophys Res Commun281678681
  47. 47. Manolio TA, Collins FS, Cox NJ, Goldstein DB, Hindorff LA, et al. (2009) Finding the missing heritability of complex diseases. Nature 461: 747–753.TA ManolioFS CollinsNJ CoxDB GoldsteinLA Hindorff2009Finding the missing heritability of complex diseases.Nature461747753
  48. 48. Hindorff LA, Sethupathy P, Junkins HA, Ramos EM, Mehta JP, et al. (2009) Potential etiologic and functional implications of genome-wide association loci for human diseases and traits. Proc Natl Acad Sci USA 106: 9362–9367.LA HindorffP. SethupathyHA JunkinsEM RamosJP Mehta2009Potential etiologic and functional implications of genome-wide association loci for human diseases and traits.Proc Natl Acad Sci USA10693629367
  49. 49. Solberg TR, Sonesson AK, Woolliams JA, Meuwissen T (2008) Genomic Selection using different markers types and densities. J Anim Sci 86: 2447–2454.TR SolbergAK SonessonJA WoolliamsT. Meuwissen2008Genomic Selection using different markers types and densities.J Anim Sci8624472454
  50. 50. Purcell S, Neale B, Todd-Brown K, Thomas L, Ferreira MAR, et al. (2007) PLINK: a toolset for whole-genome association and population-based linkage analysis. Am J Hum Genet 81: 559–575.S. PurcellB. NealeK. Todd-BrownL. ThomasMAR Ferreira2007PLINK: a toolset for whole-genome association and population-based linkage analysis.Am J Hum Genet81559575
  51. 51. Kizilkaya K, Fernando FL, Garrick DJ (2010) Genomic prediction of simulated multibreed and purebred performance using observed fifty thousand single nucleotide polymorphism genotypes. J Anim Sci 88: 544–551.K. KizilkayaFL FernandoDJ Garrick2010Genomic prediction of simulated multibreed and purebred performance using observed fifty thousand single nucleotide polymorphism genotypes.J Anim Sci88544551
  52. 52. Sun X, Habier D, Fernando RL, Garrick DJ, Dekkers JCM (2010) Genomic breeding value prediction and QTL mapping of QTLMAS2010 data using Bayesian methods. BMC proceedings (In press). X. SunD. HabierRL FernandoDJ GarrickJCM Dekkers2010Genomic breeding value prediction and QTL mapping of QTLMAS2010 data using Bayesian methods.BMC proceedings (In press)
  53. 53. Barrett JE, Fry B, Maller J, Daly MJ (2005) Haploview: analysis and visualization of LD and haplotype maps. Bioinformatics 15: 263–265.JE BarrettB. FryJ. MallerMJ Daly2005Haploview: analysis and visualization of LD and haplotype maps.Bioinformatics15263265
  54. 54. Stephens M, Smith N, Donnelly P (2001) A new statistical method for haplotype reconstruction from population data. Am J Hum Genet 69: 978–989.M. StephensN. SmithP. Donnelly2001A new statistical method for haplotype reconstruction from population data.Am J Hum Genet69978989