- Research article
- Open Access
Genomic structure and marker-derived gene networks for growth and meat quality traits of Brazilian Nelore beef cattle
BMC Genomics volume 17, Article number: 235 (2016)
- The Erratum to this article has been published in BMC Genomics 2016 17:492
Nelore is the major beef cattle breed in Brazil with more than 130 million heads. Genome-wide association studies (GWAS) are often used to associate markers and genomic regions to growth and meat quality traits that can be used to assist selection programs. An alternative methodology to traditional GWAS that involves the construction of gene network interactions, derived from results of several GWAS is the AWM (Association Weight Matrices)/PCIT (Partial Correlation and Information Theory). With the aim of evaluating the genetic architecture of Brazilian Nelore cattle, we used high-density SNP genotyping data (~770,000 SNP) from 780 Nelore animals comprising 34 half-sibling families derived from highly disseminated and unrelated sires from across Brazil. The AWM/PCIT methodology was employed to evaluate the genes that participate in a series of eight phenotypes related to growth and meat quality obtained from this Nelore sample.
Our results indicate a lack of structuring between the individuals studied since principal component analyses were not able to differentiate families by its sires or by its ancestral lineages. The application of the AWM/PCIT methodology revealed a trio of transcription factors (comprising VDR, LHX9 and ZEB1) which in combination connected 66 genes through 359 edges and whose biological functions were inspected, some revealing to participate in biological growth processes in literature searches.
The diversity of the Nelore sample studied is not high enough to differentiate among families neither by sires nor by using the available ancestral lineage information. The gene networks constructed from the AWM/PCIT methodology were a useful alternative in characterizing genes and gene networks that were allegedly influential in growth and meat quality traits in Nelore cattle.
Brazilian livestock began with taurine cattle introduced from Europe in the colonial period, around 450 years ago. Several years later, starting in 1930 but mainly in 1960 and 1962, a Bos indicus cattle breed named Nelore was introduced in Brazil from India and the herd expanded to the majority of the territory due to its good adaptability to tropical climate. It is estimated that 7000 Nelore cattle were introduced from India, the majority were descendants from 6 main sires named Karvadi, Taj Mahal, Kurupathy, Golias, Godhavari and Rasta . The Nelore, a breed with white or gray pelage and short horns, is nowadays the most representative breed in Brazil and dominates the Brazilian beef cattle production with more than 75 % of the total herd which equates to more than 130 million heads of Nelore cattle. Artificial insemination is widely used in Brazil  and semen for only a few sires has been intensively used nationwide. With the advent of the Illumina BovineHD BeadChip (Illumina Inc., San Diego, CA), a high density SNP panel comprising over 770,000 markers, we were able to measure the genomic diversity of the Brazilian Nelore from the main commercial sire families and characterize their genomic relationship and genetic profiles across a series of phenotypes. Traditional phenotype-based selection has been focused primarily on improving growth and maternal traits . However, marker-assisted or genomic selection is particularly valuable for traits that have late, onerous and expensive measurement such as meat quality, yield and feed efficiency . Despite production advantages of Bos indicus composite breeds in tropical and subtropical environments, the inferiority of beef quality, especially tenderness, is a worrying issue for producers [5, 6]. It is known that Nelore breed show moderate heritability for meat quality  as well as for growth-related traits , which make the application of genomic tools feasible.
Genome-Wide Association Studies, or GWAS, are today a common practice in order to find associations of genome regions to phenotypes of interest such as meat quality traits [7, 9, 10]. However, GWAS are sometimes elusive regarding the low power of association of the markers to the trait and also to the association of regions of the genome that lack apparent relation to the trait being studied [11, 12]. Some meta-analysis approaches are appealing as they attempt to enrich GWAS analyses with information from other sources. One of these methods is the system’s biology AWM/PCIT methodology, which involves the construction of SNP-based gene network interactions, integrating results from several GWAS by means of the Association Weight Matrices (AWM) and Partial Correlation and Information Theory (PCIT) [13–16]. We took advantage of this methodology to explore growth and meat quality traits from 780 samples of Brazilian Nelore cattle, systematically sourced to represent 34 highly influential sires and their 746 half-sibs from across Brazil. Further, we inferred a gene network focused on growth and meat quality traits and found several genes implicated in the regulation of these phenotypes.
Genetic profile of Brazilian Nelore beef cattle
After quality control filters we retained genotypes of 449,203 SNPs for linkage disequilibrium and haplotype block analysis, and 224,969 TagSNPs from 780 Nelore animals, including 34 prominent sires and their 746 progeny (Table 1). These genotypes were coupled with genotypes of the same SNP for a sample of 46 Brahman, Hereford and 44 Angus cattle sourced from the Bovine HapMap project [17, 18], and used to calculate a genomic relationship matrix (GRM) that was used in a principal component analysis (PCA) . This analysis (Fig. 1a, inset) shows that the first component, explaining 86 % of the variation in genotype profiles, separates the taurine (Angus and Hereford) from the indicine (Brahman and Nelore) breeds, indicating that the genotyping data is reliable. A GRM considering only the 780 Nelore animals and the 224,969 TagSNPs was also constructed and used for a PCA analysis exclusive for the Brazilian Nelore sample. The results for the PCA (Fig. 1a) shows that although some half-sib families are well distinguished (e.g. the NE001383, NE001398 and NE001362 families), the bulk of the samples were not well separated by the first component, indicating a lack of structuring. The first and second components only explain 8.1 % and 6.8 % of the variation respectively. It is interesting to note in Fig. 1a that the distance from a given sire (greater labeled circles) to its corresponding cluster of half-sibs is visually symmetrical to the distance of the half-sib cluster to the center of the figure. We suggest that this effect is due to the randomness diversity of the genetic effect of the dams that would bring more related individuals to the center of the figure, indicating that these sires are less related to its half-sib families and even less related to the bulk of more related individuals in the center. The average genomic inbreeding coefficient from the GRM (FGRM) reports values of 2 % (± 5 % SD) for sires and 0 % (± 3 % SD) for progeny. Also, inbreeding coefficient derived from runs of homozygosity (FROH) reports values of 9 % (± 5 % SD) for sires, and 6 % (± 2 % SD) for progeny, showing that the 34 sires are more inbred than their progeny, and that the random genetic pool from the dams brought more variability into this sample. The distribution of these inbreeding coefficients (FGRM and FROH) can be seen in Fig. 2. Additional file 1: Figure S1C depicts the pedigree with the information of the dams showing that some dams participate in more than one family.
In addition to the PCA, we performed a hierarchical cluster analysis of the GRM and plotted the resulting heatmap (Fig. 1b). This analysis shows that the 34 families are well distinguished in the heatmap (grey squares in the central diagonal) and the sire relatedness to its sibs can be distinguished in some cases by a white cross inside the central squares (e.g. NE001710 family) or a white border line for some squares that follows the red lines in the upper palette representing the sires. In overall the heatmap is greyish than what would be expected taking into account that the sires were selected to be more unrelated with each other, suggesting that the half-sib families are genetically related. Wright’s F statistic (Fst) was applied to evaluate the degree of genetic differentiation among each sire with its progeny as one population (34 populations) and each lineage with its descendants as one population (17 populations) yielding values of Fst = 0.14 and Fst = 0.09, respectively, which can be considered a small level of genetic differentiation in this Nelore sample . The clustering analysis also put together the majority of the animals evidencing the relatedness of the families. Some darker grey shades can be seen within the progeny of individual NE001383, which is the individual that is more distant in the PCA analysis, showing that this sire and its half-sibs are more unrelated to all other individuals. Although this individual sire is from the Karvadi lineage and supposed to be related to the NE001394, NE001393, NE001360 and NE001385 (see Fig. 1c), in the PCA it is more distinguished from others. Overall, the lineage information obtained from pedigree was not useful to evidence any kind of relatedness between individuals with similar ancestry. For example, nor the PCA or the hierarchical clustering show any improvement in distinguishing related and unrelated animals regarding to its lineages (Additional file 1: Figure S1A and S1B). The hierarchical clustering also does not cluster individuals according to its ancestral lineages (see for example the cluster of individuals NE001383, NE001362 and NE001398, from the Karvadi, Taj Mahal and Godar Imp lineages). One explanation for the failure of these analyses to differentiate the half-sib families is the fact that the families do not have the same number of animals and the same goes for the lineage ancestry of the families (see Table 1). These distributions could affect the effectiveness of the GRM to provide enough information to generate a good differentiation in the PCA or hierarchical cluster analyses across lineages.
We obtained information of mitochondrial DNA (mtDNA) of 30 of the 34 sires from a previous study . Results show that 23 (76.66 %) of these have Bos taurus maternal ancestry (Table 1), which agrees with the hypothesis that most of the Brazilian Nelore herd was obtained by backcrossing with females of taurine origin . Although two of the most divergent sires, NE001398 and NE001362 were of indicine maternal ancestry, in overall the maternal ancestry seems not to have influenced the PCA results. For a better characterization of the genomic data under study we analyzed the haplotype structure of the population and estimated the extent of the linkage disequilibrium (LD), decay by physical genomic distance on autosomes, as the squared correlation coefficient (r 2) between SNP pairs. Additional file 2: Figure S2 shows that LD varies from r 2 = 0.58 between SNPs distance up to 1 kb for BTA5 to r 2 = 0.03 between SNPs distance of 500 kb to 1 Mb for BTA25. The average distance between SNPs for this LD study was 5.62 kb, with large gaps of 1.08 Mb on BTA7, and of 0.9 Mb and 0.84 Mb on BTA12 and on BTA27, respectively. At the distance of 10 kb to 25 kb, the overall average r 2 was ≈ 0.30, which is considered strong LD and can be used for QTL mapping , while at distance of 25 kb to 50 kb, the overall average r 2 was ≈ 0.20, which is sufficient to provide an accuracy of 0.85 for estimation of genomic breeding value . A summary of the haplotype block description is provided on Additional file 3: Table S1. From the SNPs considered for the LD and haplotype block study, 335,179 (75 %) were clustered into haplotype blocks constituted of 3 or more SNPs, spanning 1.35 MB (54 %) of the total autosomal genome size. There were 54,461 haplotype blocks with overall average length of 24.25 kb, BTA16 (882 kb) followed by BTA4 (783 kb), and BTA5 (669 kb) presented the longest haplotype blocks, the average number of SNPs into haplotype blocks was 6, with a maximum of 111 SNPs (BTA18). The haplotype block size and distribution along autosomes is provided in Additional file 4: Figure S3.
The effective population size (Ne) was estimated to be around 214 animals in average per chromosome, with a confidence interval of 13.5, one generation ago (assuming ≈ 7 years for each generation). This number is higher than the Ne obtained from pedigree records, varying from 98 to 68, calculated from past periods of time (from 1979 to 1998)  and from another study also using pedigree records, that shows Ne to be around 120 for a Brazilian Polled Nelore breed . We estimated Ne to be higher 10 generations ago (around 270 ± 16.86 animals, in average per chromosome), when the breed was introduced in Brazil. Ne shows a decreasing pattern over the last generations especially for the last two (see Additional file 5: Figure S4).
Gene networks for growth and meat quality traits
We performed correlation analyses using the phenotype collection (see Table 2 for summary statistics) with the VCE software . Although we obtained low heritability values (h2 < 0.10) for lightness of meat (LM), lightness of fat (LF), pH (PH), cooking loss (CLO) and dressing (DRE), higher estimates were observed for rib eye area (REA; h2 = 0.55), total carcass weight (TCW; h2 = 0.26) and back fat thickness (BFT; h2 = 0.15). There was a negative correlation between BFT and REA (−0.735) and between BFT and TCW (−0.774) and a strong positive correlation between TCW and REA (0.774) which makes biological sense indicating that the data is consistent. We calculated the influence (1 % increase) of inbreeding over the phenotypes, by estimating the inbreeding depression coefficients derived from FROH and FGRM (Table 3). Only BFT, PH and CLO appeared to be significantly affected by inbreeding although this was not a consensus among the two methods of estimation. The results suggest that inbreeding did not strongly influentiate the traits.
Genome-wide association studies
The QXPAK.5 software was used  to perform genome wide association studies (GWAS) using the 224,969 TagSNPs for all eight phenotypes. Manhattan plots with the results are displayed in Fig. 3. When looking for markers with a significance threshold of p ≤ 10−3 we obtained several hundreds of significant TagSNPs, varying from 1723 (BFT) to 680 (DRE). This high number of significant markers using this significance threshold indicates some inflation of the p-values (see Additional file 6: Figure S5 for QQ-plots). If the threshold is pushed further to p ≤ 10−4 the number of significant TagSNPs fall to a few hundreds and still if a more stringent threshold is used (p ≤ 10−5) we obtain just several dozens of significant TagSNPs (see Table 2). Although we had some dozens of SNPs with very low p-values (below 10−5), the traits that had better heritabilities, like BFT, REA and TCW showed a scattered distribution of significant SNPs over the chromosomes. Other traits showed more specific regions with significant SNPs like the pH trait, showing chromosome 11 with a visual peak of significant SNPs (markers BovineHD1100009381, BovineHD1100009391, BovineHD1100009772, Hapmap25798-BTA-126388, BovineHD1100009860, p-values lower than 10−8) in the region of 31 to 32 Mb, pointing to the Follicle Stimulating Hormone Receptor (FSHR) gene, but no evidence was found in the literature linking this gene to pH of meat. Other traits like LM have some diffuse peaks in chromosomes 3, 8, 10 and 27, and LF with some less intense peaks in chromosomes 1 and 14, but the lower heritability of these traits discouraged more profound analyses of these regions.
We did a literature survey of the top 10 genes associated to the lowest p-value TagSNPs for BFT, REA and TCW. For the later we searched for the involvement of the significant genes that could influence the total carcass weight phenotype. We found the gene Serotonin Receptor 2, (HTR2A) associated to the marker BovineHD1200005266 (BTA12, p = 1e-6) which plays a role in appetite control  and was found associated to birth weight in humans . We also found the Leukemia inhibitory factor receptor (LIFR) gene, associated to the marker BovineHD2000010215 (BTA20, p = 1.21e-6) which is involved in skeletal growth and bone formation and resorption in humans . For the BFT phenotype we searched for genes involved in studies related to adipose tissue and fat. We found the gene EPHA6 (ephrin receptor a6), associated to the marker BovineHD0100011825 (BTA1, p = 1.10e-6) found associated in a copy number variation (CNV) study to childhood obesity  and the gene TMEM182 (transmembrane protein 182), associated to the marker BovineHD1100002798 (BTA11, p = 1.5e-7) which is found up-regulated in brown adipose tissue during adipogenesis and myogenesis  and also found associated in another GWAS for BFT , discussed below. We found no specific genes related to REA in the literature, that could be influencing muscle growth and myogenesis, associated to any TagSNPs of the top 10 list. In a previous work from our group , GWAS were performed using a Bayesian approach, with a subset of the data used in this work (smaller number of animals and traits). We compared the set of SNP, associated with significance below 10−5 in our work, against the ones associated in this previous work, to try to find genes simultaneously associated in both studies. We found one common gene for LM, 37 common genes for LF, 15 common genes for BFT and 12 genes for REA (gene ids at Additional file 7: Spreadsheet S1). The accordance between both works for BFT, REA and LF were of 26 %, 38 % and 38 % respectively, of all genes with significance below 10−5. We could not estimate the accordance for the TCW trait as it was not used in this previous work.
To test for Gene Ontology (GO) enrichment, we ordered all TagSNPs according to the pleiotropy test  used. The ordered list of all corresponding genes was used as input to GOrilla  and results showed “cell adhesion” (GO:0007155, false discovery rate or FDR q-value = 2.8e-4), “biological adhesion” (GO:0022610, FDR q-value = 1.52e-4) and “developmental growth” (GO:0048589, FDR q-value = 1.29e-4) as the three GO terms from the biological process tree enriched with significant values after a FDR correction. Cell adhesion was also found significantly enriched for color of muscle and fat and for meat tenderness in our previous work . For the list of genes in each GO, check Additional file 8: Spreadsheet S2.
For a more holistic view of the genes influencing the eight phenotypes related to growth and meat quality we used the p-values and SNP additive effects (Z scored) obtained with the QXPAK.5 software to construct an AWM (see Additional file 9: Spreadsheet S3 for the list of SNP additive effects and p-values respectively used in the AWM). TCW was chosen as key phenotype for the AWM which was then used to calculate a pair-wise correlation matrix of all SNP effects. This correlation matrix was first filtered to maintain genes with correlation values equal or above 0.95. It was then used to run the PCIT methodology, which generated a gene network that consisted of 3371 genes (nodes) and 6961 gene relationships (edges) (data not shown). This is allegedly the network that contains genes more involved in growth traits because of the key phenotype (TCW), and also prone to be constituted of genes more involved with traits highly correlated to TCW, like REA and BFT. With less intensity, the network is supposed to contain genes involved with the other five phenotypes as they are less correlated to TCW. Additional file 10: Figure S6 shows a heatmap and hierarchical cluster obtained with the standardized SNP effects of the eight phenotypes that evidences that TCW, REA and BFT are more correlated than pH, CLO, LF, LM and DRE.
For visualization we used Cytoscape v3.1 and applied several visual filters to identify highly connected nodes. We suggest that the number of connections is a measure of the importance of the node to the function of the network as a whole. The assumption is that the more connections a gene has the more likely is its role regulating and influencing the function of other genes in the network. After applying the filters, the size of the node was changed to be proportional to its number of edges. The smaller the number of connections of a node, the smaller was the size of the node and vice-versa. This same rule is valid for the coloring: the more reddish, more connections and the more greenish, less connections. The obtained network shows in its center, a cluster of nodes with larger size and stronger red color intensity showing that these nodes are more interconnected and are probably more involved in key biological mechanisms underlying the phenotypes involved in the network (data not shown).
As an alternative type of analysis found in similar works [35–37], we decided to divide the network in a smaller sub-network to focus on a specific set of genes that have the highest degree of connections. We used an algorithm to select the trio of transcription factors that mostly span the network with minimum redundancy . Transcription factors (TF) are known to regulate several cellular mechanisms in different degrees. We arbitrarily decided to select three TF with most connections, which is a number that results in a sub-network with a reasonable sampling of the more important genes involved with the phenotypes. We used Cytoscape to create the sub-network by selecting the TF trio including the edges shared among its first degree nodes. The resulting sub-network, with 66 nodes and 359 edges, is shown in Fig. 4. Colors and node sizes represent the levels of connections inherited from the original network and triangular shaped nodes are representing the TF. The trio of TF chosen by our algorithm is composed by the VDR (Vitamin D Receptor), LHX9 (Lim Homeobox) and ZEB1 (Zinc finger E-box binding homeobox 1) genes. The VDR, or Vitamin D (1,25- Dihydroxyvitamin D3) Receptor is a hormone receptor for vitamin D3 and is a transcription factor involved in a variety of metabolic pathways. Mutations in the VDR gene can lead to the rickets disease, characterized by growth retardation, bone deformity among other effects  and this gene was also found related to bone density in mice . More interestingly, SNPs in the coding region of VDR were found to be associated with growth traits in bovine . The LHX9 gene is a transcription factor involved in developmental processes like neuronal and gonadal development [42, 43] and also to limb three-dimensional patterning and growth  in mice. Taken together, the known functions of LHX9 are implicated in several important growth and developmental mechanisms which suggests it is an important player in the growth trait phenotype network. The other TF from the most connected TF trio is the ZEB1 (Zinc Finger E-Box Binding Homeobox 1), a zinc finger transcription factor which is involved in cancer and in regulation of the expression of several genes (check the entry for [Uniprot:P37275] at http://www.uniprot.org), this gene have been related to muscle differentiation and myogenesis .
From the set of genes with direct edges to the trio of TF, there are some genes with remarkable evidence in literature relating them to growth traits, specially bone and muscle growth and adipogenesis. The ASB2 (ankyrin repeat and SOCS box containing 2), is a gene found to function in a negative regulation of muscle growth in salmon . The PROCR gene (protein C receptor, endothelial) was found to positively regulate other genes positively, in an osteoblastic cell line, functioning toward bone growth . The ALDH9A1 (aldehyde dehydrogenase 9 family, member A1), has a role on fetal growth in adult adipose tissue mass in bovine . CPEB4, or cytoplasmic polyadenylation element binding protein 4, is associated to human waist-hip ratio . The leucine-rich repeat LGI family, member 3, LGI3, is thought to have its function altered in obesity and to suppress adipogenesis . GPC6 (glypican 6) is implicated in bone growth . The FAM3C gene, or Family With Sequence Similarity 3, Member C was found associated to influence bone mineral density in humans . A gene, the IARS (isoleucyl-tRNA synthetase), was found related to perinatal weak calf syndrome, which involves intrauterine growth retardation and low birth weights . There are several other genes related to cell growth and proliferation, like ERGIC3 (ERGIC and golgi 3) , KHDRBS3 (KH domain containing, RNA binding, signal transduction associated 3) , CEP250 (centrosomal protein 250 kDa) , STIM2 (stromal interaction molecule 2) , HABP2 (hyaluronan binding protein 2) .
From all 66 genes present in this sub-network, 33 were found also associated to REA (32 genes) and BFT (1 gene) in the work from Tizioto et al., 2013 . The rib eye area associated genes include the already discussed: VDR, ASB2, ALDH9A1, CPEB4, GPC6, FAM3C, IARS, KHDRBS3, CEP250 and STIM2. Only one gene was also found associated to BFT, EPB41L1 or Erythrocyte Membrane Protein Band 4.1-Like, which was found related to growth regulation . Taken together, all the evidence found in literature of the relatedness of these genes to growth traits suggests that our methodology is reliable and the gene networks obtained shed a light on the biological mechanisms beyond growth and meat quality traits. Furthermore, as can be seen in Table 4, the SNPs that correspond to the best trio of TF have mostly p-values above 1e-3 meaning that this methodology captures SNPs that would not be taken as important by traditional GWAS.
After the introduction of the Nelore breed in Brazil in the last century, there were some pedigree-based studies trying to characterize the founder lineages of the breed , but no genomic approach has been made since then. The introduction of the low and high density bovine genotyping panels, made possible the calculation and use of GRM matrices  in genomic similarity studies to create a genetic profile. Using only pedigree information from the 34 sires, the average inbreeding coefficient (FPED) was 3.23 % (± 3.9 SD) (calculation performed during experimental design, not shown), which is similar to the FGRM reported for sires, but lower than the FROH reported for sires. Comparing the inbreeding coefficients between sires and progeny, there is a clear decrease in inbreeding, which can only be attributed to the randomness of the genetic pool of the dams. According to recent literature, FGRM was determined as the optimal method for estimating genomic inbreeding coefficients as it can distinguish between markers that are IBS (identical by state) from markers that are IBD (identical by descendent) [61, 62]. The average FROH for either sires or progeny estimated in this study are higher than the ones reported for a Holstein population (3.8 ± 2.1 %) which have shown effects of inbreeding depression for traits in dairy cattle . Also, inbreeding depression appears not to have strongly affected the phenotypes (Table 3). This result agrees with the lower inbred estimation for the progeny compared to the sires. We were not able to cross test this hypothesis by estimating inbreeding depression for the traits among sires, as we did not collect their phenotypes, altough we would expect a stronger influence of inbreeding in this case.
The average r 2 values obtained in this study, considering SNPs with distance up to 150 kb apart, are higher than the values reported in the literature for Nelore and indicine breeds. Beyond 150 kb distance, the average r 2 values are similar to ones found in the literature [63, 64]. However, it is worth mentioning that it is difficult to make direct comparisons among LD studies, as LD levels vary due to many factors (sample size, marker type, marker density, and population history) . In this study, both maternal and paternal haplotypes were considered in contrast to studies that only consider maternal haplotypes, as it is our understanding that the Nelore population (and cattle production in general) presents higher influence from males than females and not considering paternal haplotypes would underestimate r 2 values. We believe that the backcrossing with taurine local breeds, evidenced by the mtDNA origin, could have influenced the values of LD and Ne estimated for this Nelore sample.
There are some reports in the literature considering haplotype block structure in cattle, but none was found for Nelore cattle. These reports stated that with the increase in marker density, there will be more haplotype blocks of smaller sizes which will respond for higher genome coverage [66–68]. A recent study using the high density SNP panel in crossbred cattle population reports 61 % of the genome covered by haplotype blocks, and a total of 78 % of SNPs clustered into haplotype blocks . The recent Ne found for Nelore in this study, is in agreement with reports of recent Ne for Holstein and Swiss Eringer breed varying from 80 to 150 individuals, and can go higher than 2000 animals for past Ne (about 2000 generations ago) [67, 70, 71]. Our results show that the diversity among sire families and lineages is not high enough to correctly separate those in a PCA, or hierarchical clustering analysis (Fig. 1). This is corroborated by the low Fst values obtained for sire families and lineages subpopulations. The uninformative values of Ne and Fst estimates were expected for the lineages as they do not represent isolated populations and should have been crosses among them.
Some of the traits used in this work were already analyzed for genome wide associations elsewhere using part of the data and with a different approach . Although the phenotype data is the same in both works, our sample size was larger and the software and algorithms used for association studies were different. We have not found larger accordance than 38 %, between the set of associated genes with significance of 1e-5 to BFT, REA and LM traits, studied in that work, although we could not verify this for TCW as this trait was not present in that work. However, the quality and consistency of the genotyping data were found reliable since the PCA against other breeds showed consistent results (Fig. 1a, inset). We also checked for the fluctuation of heterozygosity along the 224,969 TagSNPs and found reasonable smoothed values of heterozygosity fluctuating around 0.3 to 0.4 (Additional file 11: Figure S7). The traits correlations were also found reasonable (see Results). Furthermore some of the top TagSNPs that had lowest p-values in the GWAS, had the corresponding gene with functional biological correlation to the main growth traits, indicating that the GWAS was able to extract some of the signal out of the noise from the data. In addition, we also performed a gene enrichment test with GOrilla, after ordering the TagSNPs for the pleiotropic effect. The pleiotropic test is a methodology to try to rank genes that are most influencing the traits in the AWM. The results showed GO terms for biological and cell adhesion and developmental growth, which are again evidence that the terms are enriched for genes related mainly to growth which is the key phenotype of the AWM. Cell adhesion is a biological process that is also found significantly enriched in the work of Tizioto et al., 2013 . Cell adhesion is a process involved in the binding of a cell to a substrate which sustains its growth and therefore is intrinsically related to the growth process.
With a similar objective of the pleiotropy test, the construction of the gene networks with the AWM/PCIT [13, 35–37] is an alternative to analyze pure GWAS results as this methodology gathers the 8 GWAS results and constructs a gene network that influences the traits in a simultaneous way, but weighting accordingly to the correlations within the AWM. We decided to select TCW as the key trait for the AWM because of its reasonable heritability estimate and its congruent correlations to REA and BFT, together with the economic importance of growth traits for livestock. As the resulting network is too large (3371 nodes), we used a heuristic to divide the network into a sub-network in a way that it would be feasible to analyze and still gather most of the biological importance regarding these traits. This heuristic is implemented in an algorithm that selects the trio of TF that most span the network and its first degree nodes. As the coloring and shape of the nodes of the resulting sub-network are inherited from the original network, it can be noticed a majority of reddish and larger nodes (with more connections) indicating that the objective of the heuristic was achieved (Fig. 4). Also, a survey in the literature showed correlations between the trio of TF and several nodes from the sub-network to growth traits, suggesting that our methodology is correct. It is remarkable to note that some genes like VDR (which is the most connected TF from the network) was already associated to growth in a bovine GWAS  and many others have relations to the biology of growth, like proliferation and growth of muscle and bones and adipogenesis (e.g. LHX9, CPEB4, ASB2, and many others). Although comparing the results of single SNP association to the work of Tizioto et al. 2013 did not lead to more than 38 % of common associated genes, the genes from the sub-network are in 50 % of accordance with the genes associated to BFT and REA from that work. This suggests that the methodology that created this network was able to select genes that are more related to the traits involved with growth. We compared the genes from the sub-network to genes found in other studies [35–37] that also used the AWM/PCIT methodology and similar datasets (but different breeds). Although there were no great correlations, some genes in these studies were found to have similarities or to encode the same protein domains to some of the genes from the sub-network: metalloprotease and ankyrin domains (genes ADAMTS14 and ASB2 respectively), the RAB6B oncogene , the MER Proto-Oncogene Tyrosine Kinase (MERTK) and the SLC solute carrier gene family (SLC34A2) .
Taken together, these results are suggesting that the gene networks obtained are related to growth and meat quality traits and their genes should be thoroughly inspected to try to discover the biological mechanism beneath growth and meat quality phenotypes.
We used high density SNP panels to genotype 34 sires, and its half-sib families, totaling 780 animals. The sires were previously selected in order to represent most of the variability of the Nelore beef cattle in Brazil. We believe this is the first work that used a genomic approach in order to try to investigate the amount of diversity of the Brazilian Nelore breed by investigating its ancestral lineages. Results showed that the population studied was not structured enough in order to differentiate families using ancestral information of sires or lineages. Eight phenotypes related to growth and meat quality were used in whole genome association studies and the results were used to construct gene networks focused on growth, using the methodology of AWM/PCIT. Literature surveys showed that both the GWAS and the gene networks constructed had significant SNPs associated to genes related to growth in former studies like the VDR, LHX9, CPEB4, ASB2 and many others. These results suggests that the methodology used to construct the gene networks can be used as an alternative approach to standard GWAS, in order to reach for novel information and to try to understand the biological mechanisms and gene compositions that leads to complex phenotypes, like growth in beef cattle.
Pedigree and sire lineages
Aiming to select sires that represent the bulk of genetic variability within the Nelore breed in Brazil, we consulted the main insemination centers of the country, selecting the more commercially frequent Nelore sires (polled and horned), with semen value equal or inferior to R$50.0 (around US$25.0 at the time of the study) to represent the breeders preference. Afterwards, using information from the National Zootechnical File maintained by Embrapa Beef Cattle in partnership with ABCZ (Brazilian Association of Zebu Breeders) the pedigree of all animals were assembled and a relationship pedigree matrix was created (data not shown). The sires were selected by the following rules: having the most commercialized semen among the breeders association in Brazil and ii) being the most unrelated with each other according to the value of similarity from the pedigree relationship matrix.
A list of 34 sires was assembled representing almost all lineages of the Nelore breed in Brazil (see Table 1): Karvadi, Taj Mahal, Golias, Padhu-Akasamu, Kurupathy, NO, Godar, Godhavari, Mocho GR, Nagpur, Akasamu, Padhu, Lengruber (Mundo Novo), Visual, OB, IZ and IRCA. The sire lineage was surveyed by following information about the most ancestral sire from the paternal side. Our sample study was composed of 34 sires and half-sib families with 746 animals in a total of 780 animals. The 746 calves, sons of commercial cows (not pure Nelore), were born on five different ranches, where they were raised to around 21 months old, before allocation to individual or collective pens in a feedlot located in Sao Carlos, SP, Brazil; or in Campo Grande, MS, Brazil, in an interval of 3 years. The pedigree was visualized with Cytoscape version 3.1 .
The mtDNA genotype was characterized as taurine (GenBank AY526085) or indicine (GenBank AY126697) from total DNA by amplification of a 366 bp fragment of mtDNA 16S (rRNA) gene using allele-specific PCR. The complete methodology can be found in .
Eight phenotypes related to growth and meat quality were collected: Total Carcass Weight (TCW, Kg); Dressing percentage (DRE, %); Rib Eye Area (REA, cm2); Back Fat Thickness (BFT, mm); Lightness of Meat (LM); Lightness of Fat (LF); pH (PH); Cooking Loss (CLO, %). The phenotypes were collected as described elsewhere , see Table 2. The number of animals with phenotype measurements varied around 670. The VCE software (ftp://ftp.tzv.fal.de/pub/vce6/) was used to calculate the correlations between phenotypes, the heritabilities and the respective standard errors (SE). The model used was the following (Equation 1):
Where y is a vector with the values for a given phenotype, X and Z are incidence matrix, β is a vector for fixed effects composed of the first principal component used as co-variate, Slaughter Age also a co-variate, the contemporary group effect is represented by Origin * Year of Birth and Animal ID, representing the pedigree. g is a vector of additive genetic effects, normally distributed g ~ N(0, σ 2 g ). E represent the vector of residual effects, E ~ N(0, σ 2 e ).
Genotyping and quality control
All 34 sires and 746 half-sibs were genotyped with a high density SNP panel (Illumina Bovine HD SNP Chip). The DNA sample collection and the SNP chip genotyping were performed as previously described . We used quality control filters for minor allele frequency (5 %) and call rate for sample and SNPs (95 %). Filters were applied using PLINK  and Biocoductor/R [74, 75]. This filters yielded a dataset comprised of 449,203 SNPs which was used for linkage disequilibrium and haplotype block description using BEAGLE  for genotype phasing and missing genotype imputation and LDexplorer  for haplotype block recognition following Gabriel et al. 2002  algorithm, and for estimating effective population size (Ne) according to .
Genomic relationship matrix
The genomic relationship matrix (GRM) was constructed [60, 80] using the TagSNPs. The GRM was used to estimate genomic inbreeding coefficient (FGRM), estimated as the diagonal elements of the GRM , and to perform PCA analyzes with all 780 Nelore samples and the same TagSNPs for 46 samples of the Brahman breed, 36 samples of Hereford breed and 44 samples of Angus breed, genotyped with the same high density SNP panel from the Hapmap project .
Genome Wide Association Study (GWAS)
All GWAS were performed using the software QXPAX5 . Although we have used the first principal component of the PCA analysis as covariate to correct for population substructure bias , we needed to perform a manual correction to fix for contemporary group substructure bias, as follows. We calculated the mean phenotype value for each contemporary group and the raw phenotype value of every animal from a given group was subtracted from its correspondent mean contemporary group value. The model used was the one that follows (Equation 2), now without the contemporary group covariate:
Where y ' is a vector containing the phenotype corrected for the contemporary group effect from the i-th animal to the j-th trait (check Table 2), X is the incidence matrix relating fixed effects in β' with observations in y' ij . β' is a vector for fixed effects composed of the first principal component used as co-variate, slaughter age also a co-variate, representing the pedigree. Z is the incidence matrix relating random additive polygenic effects in g with the observations in y' ij . g is a vector composed of the additive genetic effects, normally distributed g ~ N(0, Aσ 2 g ); were A represents the numerator relationship matrix derived from the pedigree. S k is the vector of genotypes for the k-th SNP across all animals. s jk is a vector that represents the additive effect of the k-th SNP on the j-th trait and E represents the vector of residual effects, E ~ N(0, σ 2 e ). QXPAK5 was run for the eight phenotypes using the TagSNP set. The p-values and additive genetic values for each SNP were obtained for each phenotype and used to construct the AWM matrix. The FDR (false discovery rate) was calculated using the formula of .
AWM/PCIT and gene networks
AWM is a methodology to explore the results obtained from several GWAS (many traits) and generate a matrix of genes (or SNPs) co-associated in a pair-wise manner to these traits. The rows in the AWM are composed of the genes (or SNPs) and the columns represent the traits. The AWM matrix is filled with the additive effects of the SNPs. AWM was used to select SNPs associated to the key trait (TCW) and also SNPs associated to several (three or more) other traits. This was done in order to keep SNPs that are important to “growth” in a holistic manner. Afterwards, a pair-wise Pearson’s correlation is calculated and the data is submitted to PCIT that is a network inference methodology used to construct the gene network. The AWM was constructed as described elsewhere . The correlation matrix was calculated for every entry of the AWM, using the standardized Z score (the additive SNP effect divided by the standard deviation) within the R environment. The correlation matrix was used as input for the PCIT package for R . A list of genes that correspond to each TagSNPs were obtained from Ensembl version 74 (http://www.ensembl.org), where genes were assigned to its nearest TagSNP. Gene networks generated by PCIT were visualized with Cytoscape version 3.1 . A transcription factor list was obtained from the Animal Transcription Factor Database  and the most connected trio of transcription factors from the gene network was obtained as described elsewhere .
Pleiotropy and gene enrichment
To test for pleiotropy we employed the approach described by . In brief, the effects of the 224,969 TagSNPs estimated from the GWAS were divided by their associated standard errors to obtain a t-value corresponding to the studentized SNP effects. A multi-trait test of the i-th TagSNP was performed by storing its studentized effects across the 8 traits in the 8 x 1 vector t i. Then, the quadratic form t i 'V − 1 t i , where V is the correlation matrix among the SNP effects, is distributed approximately as a chi-squared with 8 df under the null hypothesis that the TagSNP does not affect any of the traits . The TagSNPs where then ordered according to the results and the ordered list of corresponding genes were used as input to GOrilla .
Linkage disequilibrium and other analyses
The relationship between LD (r 2) and Ne can be expressed by the Equation 3:
where, c is the genetic distance between two SNP expressed in Morgans . Considering each SNP pairs located within 100Mbp of the same autosomal chromosomes, with physical distances between SNP converted to genetic distances by the simple assumption of 1 cM ~ 1 Mb were used for Ne estimation. Haploview was used for obtaining TagSNPs, which were used for deriving inbreeding coefficient by runs of homozygozity (FROH), calculated with PLINK, as described by . Heterozygosity changes along the 224,969 TagSNPs were calculated with PLINK and plotted in R using a smoothing function from the lokern package, one point for each 100 TagSNPs, as described elsewhere . The Wright’s F statistics (Fst) analyses were run with PLINK 1.9 (https://www.cog-genomics.org/plink2) using the TagSNPs of the 780 animals, separated: i) by lineage (17 subpopulations) and ii) by sire families (34 subpopulations).
All experimental procedures involving steers were approved by the Institutional Animal Care and Use Committee Guidelines from Brazilian Agricultural Research Corporation – EMBRAPA and sanctioned by the president of the committee, Dr. Rui Machado.
Availability of supporting data
The data set supporting the results of this article is included within the article (and its additional files). Genotypic data is available upon request depending on a signed declaration of exclusive research purpose.
Brazilian Association of Zebu Breeders
Association Weight Matrices
back fat thickness
false discovery rate
average genomic inbreeding coefficient from the GRM
average inbreeding coefficient derived from pedigree
inbreeding coefficient derived from runs of homozygosity
Wright’s f statistic
genomic relationship matrix
genome wide association studies
identical by descendent
identical by state
effective population size
principal component analysis
partial correlation and information theory
- r 2 :
squared correlation coefficient
rib eye area
single nucleotide polymorphism
total carcass weight
Magnabosco CU, et al. Catalogo de linhagens do germoplasma zebuino: raca Nelore, Documentos, 23. Brasilia: Embrapa-Cenargen; 1997. p. 1–52.
Foote RH. The history of artificial insemination: Selected notes and notables. J Anim Sci. 2002;80(E-Suppl 2):1–10.
Decker JE, et al. A novel analytical method, Birth Date Selection Mapping, detects response of the Angus (Bos taurus) genome to selection on complex traits. BMC Genomics. 2012;13:606.
Bolormaa S, et al. Detection of chromosome segments of zebu and taurine origin and their effect on beef production and growth. J Anim Sci. 2011;89(7):2050–60.
O'Connor SF, et al. Genetic effects on beef tenderness in Bos indicus composite and Bos taurus cattle. J Anim Sci. 1997;75(7):1822–30.
Johnson DD, et al. Effects of percentage Brahman and Angus breeding, age-season of feeding and slaughter end point on meat palatability and muscle characteristics. J Anim Sci. 1990;68(7):1980–6.
Tizioto PC, et al. Genome scan for meat quality traits in Nelore beef cattle. Physiol Genomics. 2013;45(21):1012–20.
Utsunomiya YT, et al. Genome-wide association study for birth weight in Nellore cattle points to previously described orthologous genes affecting human and bovine height. BMC Genet. 2013;14:52.
Kim Y, et al. Genome-wide association study reveals five nucleotide sequence variants for carcass traits in beef cattle. Anim Genet. 2011;42(4):361–5.
Bolormaa S, et al. A genome-wide association study of meat and carcass traits in Australian cattle. J Anim Sci. 2011;89(8):2297–309.
Barendse W. Haplotype analysis improved evidence for candidate genes for intramuscular fat percentage from a genome wide association study of cattle. PLoS One. 2011;6(12):e29601.
Wang K, Li M, Hakonarson H. Analysing biological pathways in genome-wide association studies. Nat Rev Genet. 2010;11(12):843–54.
Fortes MR, et al. Association weight matrix for the genetic dissection of puberty in beef cattle. Proc Natl Acad Sci U S A. 2010;107(31):13642–7.
Fortes MR, et al. Gene network analyses of first service conception in Brangus heifers: use of genome and trait associations, hypothalamic-transcriptome information, and transcription factors. J Anim Sci. 2012;90(9):2894–906.
Reverter A, Chan EK. Combining partial correlation and an information theory approach to the reversed engineering of gene co-expression networks. Bioinformatics. 2008;24(21):2491–7.
Watson-Haigh NS, Kadarmideen HN, Reverter A. PCIT: an R package for weighted gene co-expression networks based on partial correlation and information theory approaches. Bioinformatics. 2010;26(3):411–3.
Gibbs RA, et al. Genome-wide survey of SNP variation uncovers the genetic structure of cattle breeds. Science. 2009;324(5926):528–32.
Porto-Neto LR, et al. Genomic divergence of zebu and taurine cattle identified through high-density SNP genotyping. BMC Genomics. 2013;14:876.
Paschou P, et al. PCA-correlated SNPs for structure identification in worldwide human populations. PLoS Genet. 2007;3(9):1672–86.
El Mousadik A, Petit RJ. High level of genetic differentiation for allelic richness among populations of the argan tree [Argania spinosa (L.) Skeels] endemic to Morocco. Theor Appl Genet. 1996;92(7):832–9.
Tizioto PC, et al. Caracterizacao do haplotipo mitocondrial de uma amostra de touros da raca nelore representativa das principais linhagens comercializadas no Brasil. Ciencia Animal. 2011;21(1):25–9.
Meirelles FV, et al. Is the American Zebu really Bos indicus? Genet Mol Biol. 1999;22:543–6.
Ardlie KG, Kruglyak L, Seielstad M. Patterns of linkage disequilibrium in the human genome. Nat Rev Genet. 2002;3(4):299–309.
Meuwissen TH, Hayes BJ, Goddard ME. Prediction of total genetic value using genome-wide dense marker maps. Genetics. 2001;157(4):1819–29.
Faria FJ, et al. Pedigree analysis in the Brazilian Zebu breeds. J Anim Breed Genet. 2009;126(2):148–53.
Faria FJC, et al. Estrutura populacional da ra\cca Nelore Mocho. Arquivo Brasileiro de Medicina Veterin\'aria e Zootecnia. 2002;54:501–9.
Neumaier A, Groeneveld E. Restricted maximum likelihood estimation of covariances in sparse linear models. Genet Sel Evol. 1998;30(1):3–26.
Perez-Enciso M, Misztal I. Qxpak.5: old mixed model solutions for new genomics problems. BMC Bioinformatics. 2011;12:202.
Gasque G, et al. Small molecule drug screening in Drosophila identifies the 5HT2A receptor as a feeding modulation target. Sci Rep. 2013;3:srep02120.
Sims NA, Johnson RW. Leukemia inhibitory factor: a paracrine mediator of bone metabolism. Growth Factors. 2012;30(2):76–87.
Glessner JT, et al. A genome-wide study reveals copy number variants exclusive to childhood obesity cases. Am J Hum Genet. 2010;87(5):661–6.
Wu Y, Smas CM. Expression and regulation of transcript for the novel transmembrane protein Tmem182 in the adipocyte and muscle lineage. BMC Res Notes. 2008;1:85.
Bolormaa S, et al. A multi-trait, meta-analysis for detecting pleiotropic polymorphisms for stature, fatness and reproduction in beef cattle. PLoS Genet. 2014;10(3):e1004198.
Eden E, et al. GOrilla: a tool for discovery and visualization of enriched GO terms in ranked gene lists. BMC Bioinformatics. 2009;10:48.
Ramayo-Caldas Y, et al. A marker-derived gene network reveals the regulatory role of PPARGC1A, HNF4G, and FOXP3 in intramuscular fat deposition of beef cattle. J Anim Sci. 2014;92(7):2832–45.
Widmann P, et al. A systems biology approach using metabolomic data reveals genes and pathways interacting to modulate divergent growth in cattle. BMC Genomics. 2013;14:798.
Widmann P, et al. Systems biology analysis merging phenotype, metabolomic and genomic data identifies Non-SMC Condensin I Complex, Subunit G (NCAPG) and cellular maintenance processes as major contributors to genetic variability in bovine feed efficiency. PLoS One. 2015;10(4), e0124574.
Reverter A, Fortes MR. Breeding and Genetics Symposium: building single nucleotide polymorphism-derived gene regulatory networks: Towards functional genomewide association studies. J Anim Sci. 2013;91(2):530–6.
Malloy PJ, et al. A unique insertion/duplication in the VDR gene that truncates the VDR causing hereditary 1,25-dihydroxyvitamin D-resistant rickets without alopecia. Arch Biochem Biophys. 2007;460(2):285–92.
Yamamoto Y, et al. Vitamin D receptor in osteoblasts is a negative regulator of bone mass control. Endocrinology. 2013;154(3):1008–20.
Gao Y, et al. Two novel SNPs in the coding region of bovine VDR gene and their associations with growth traits. J Genet. 2013;92(2):e53–9.
Birk OS, et al. The LIM homeobox gene Lhx9 is essential for mouse gonad formation. Nature. 2000;403(6772):909–13.
Retaux S, et al. Lhx9: a novel LIM-homeodomain gene expressed in the developing forebrain. J Neurosci. 1999;19(2):783–93.
Tzchori I, et al. LIM homeobox transcription factors integrate signaling events that control three-dimensional limb patterning and growth. Development. 2009;136(8):1375–85.
Siles L, et al. ZEB1 imposes a temporary stage-dependent inhibition of muscle gene expression and differentiation via CtBP-mediated transcriptional repression. Mol Cell Biol. 2013;33(7):1368–82.
Bower NI, Johnston IA. Discovery and characterization of nutritionally regulated genes associated with muscle growth in Atlantic salmon. Physiol Genomics. 2010;42A(2):114–30.
Lee YJ, et al. Activated protein C differentially regulates both viability and differentiation of osteoblasts mediated by bisphosphonates. Exp Mol Med. 2013;45:e9.
Taga H, et al. Cellular and molecular large-scale features of fetal adipose tissue: is bovine perirenal adipose tissue brown? J Cell Physiol. 2012;227(4):1688–700.
Heid IM, et al. Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution. Nat Genet. 2010;42(11):949–60.
Kim HA, et al. Leucine-rich glioma inactivated 3 regulates adipogenesis through ADAM23. Biochim Biophys Acta. 2012;1821(6):914–22.
Dwivedi PP, Lam N, Powell BC. Boning up on glypicans-opportunities for new insights into bone biology. Cell Biochem Funct. 2013;31(2):91–114.
Zhang LS, et al. A follow-up association study of two genetic variants for bone mineral density variation in Caucasians. Osteoporos Int. 2012;23(7):1867–75.
Hirano T, et al. Mapping and exome sequencing identifies a mutation in the IARS gene as the cause of hereditary perinatal weak calf syndrome. PLoS One. 2013;8(5):e64036.
Nishikawa M, et al. Identification and characterization of endoplasmic reticulum-associated protein, ERp43. Gene. 2007;386(1-2):42–51.
Baudet ML, et al. Growth hormone action in the developing neural retina: a proteomic analysis. Proteomics. 2008;8(2):389–401.
Kumar A, et al. CEP proteins: the knights of centrosome dynasty. Protoplasma. 2013;250(5):965–83.
Mancarella S, et al. Targeted STIM deletion impairs calcium homeostasis, NFAT activation, and growth of smooth muscle. FASEB J. 2013;27(3):893–906.
Kannemeier C, et al. Factor VII-activating protease (FSAP) inhibits growth factor-mediated cell proliferation and migration of vascular smooth muscle cells. FASEB J. 2004;18(6):728–30.
Sun CX, Robb VA, Gutmann DH. Protein 4.1 tumor suppressors: getting a FERM grip on growth regulation. J Cell Sci. 2002;115(Pt 21):3991–4000.
VanRaden PM. Efficient methods to compute genomic predictions. J Dairy Sci. 2008;91(11):4414–23.
Keller MC, Visscher PM, Goddard ME. Quantification of inbreeding due to distant ancestors and its detection using dense single nucleotide polymorphism data. Genetics. 2011;189(1):237–49.
Bjelland DW, et al. Evaluation of inbreeding depression in Holstein cattle using whole-genome SNP markers and alternative measures of genomic inbreeding. J Dairy Sci. 2013;96(7):4697–706.
Espigolan R, et al. Study of whole genome linkage disequilibrium in Nellore cattle. BMC Genomics. 2013;14:305.
Porto-Neto LR, Kijas JW, Reverter A. The extent of linkage disequilibrium in beef cattle breeds using high-density SNP genotypes. Genet Sel Evol. 2014;46:22.
Pritchard JK, Przeworski M. Linkage disequilibrium in humans: models and data. Am J Hum Genet. 2001;69(1):1–14.
Villa-Angulo R et al. High-resolution haplotype block structure in the cattle genome. BMC Genet. 2009;10:19.
Qanbari S, et al. The pattern of linkage disequilibrium in German Holstein cattle. Anim Genet. 2010;41(4):346–56.
Lu D, et al. Linkage disequilibrium in Angus, Charolais, and Crossbred beef cattle. Front Genet. 2012;3:152.
Mokry FB, et al. Linkage disequilibrium and haplotype block structure in a composite beef cattle breed. BMC Genomics. 2014;15 Suppl 7:S6.
Goddard ME, et al. Can the same genetic markers be used in multiple breeds? In: Proc. 8th World Congr. Genet. Appl. Livest. Prod., Belo Horizonte, Brazil. 2006. CD-ROM communication no. 22-16.
Flury C, et al. Effective population size of an indigenous Swiss cattle breed estimated from linkage disequilibrium. J Anim Breed Genet. 2010;127(5):339–47.
Shannon P, et al. Cytoscape: a software environment for integrated models of biomolecular interaction networks. Genome Res. 2003;13(11):2498–504.
Purcell S, et al. PLINK: a tool set for whole-genome association and population-based linkage analyses. Am J Hum Genet. 2007;81(3):559–75.
Clayton D. snpStats: SnpMatrix and XSnpMatrix classes and methods. 2013.
Higa RH, et al. An R script for quality control in genome-wide association studies, in Proc. X-Meeting 2011 7th International Conference of the Brazilian Association for Bioinformatics and Computational Biology (AB3C), Florian\'opolis, Brazil. 2011. Online Abstract #32.
Browning SR, Browning BL. Rapid and accurate haplotype phasing and missing-data inference for whole-genome association studies by use of localized haplotype clustering. Am J Hum Genet. 2007;81(5):1084–97.
Taliun D, Gamper J, Pattaro C. Efficient haplotype block recognition of very long and dense genetic sequences. BMC Bioinformatics. 2014;15:10.
Gabriel SB, et al. The structure of haplotype blocks in the human genome. Science. 2002;296(5576):2225–9.
Badke YM, et al. Estimation of linkage disequilibrium in four US pig breeds. BMC Genomics. 2012;13:24.
Porto-Neto LR, et al. Detection of signatures of selection using Fst. Methods Mol Biol. 2013;1019:423–36.
Price AL, et al. Principal components analysis corrects for stratification in genome-wide association studies. Nat Genet. 2006;38(8):904–9.
Reverter A, Fortes MRS. Association weight matrix: a network-based approach towards functional genome-wide association studies. Methods Mol Biol. 2013;1019:437–47.
Zhang HM et al. AnimalTFDB: a comprehensive animal transcription factor database. Nucleic Acids Res. 2012;40(Database issue):D144–9.
Sved JA. Linkage disequilibrium and homozygosity of chromosome segments in finite populations. Theor Popul Biol. 1971;2(2):125–41.
This study was conducted with funding from EMBRAPA (Macroprograma1, 01/2005) and FAPESP (process number 2012/23638-8). GBM, LLC, LCAR and MMA were granted CNPq fellowships. We thank Sean McWilliam, Marina R. S. Fortes, Edilson Guimaraes, Robson Rodrigues Santiago, Roselito F. da Silva, Fernando F. Cardoso, Flavia Aline Bressani, Wilson Malago Jr., Avelardo U. C. Ferreira, Michel E. B. Yamaguishi and Fabio D. Vieira for the help and technical assistance. The authors would like to acknowledge the collaborative efforts among EMBRAPA, University of Sao Paulo and CSIRO.
The authors declare that they have no competing interests.
MAM, LRPN and FBM performed data analysis, participated in the experimental design of the study and drafted the manuscript. PCT and PSNO performed experiments, data analysis and helped to draft the manuscript. RRT, RTN, SCMN, MMA, ANR, GLDF, ALJF, LOCS, SRM, DPL, MLN, ASC, ARDLS, RAATJ and FS performed experiments. PT, GBM and RHH performed data analysis. IUP and LLC participated in the conception and experimental design of the study, LLC also contributed to the discussion of the results. ARG and LCAR participated in the experimental design and coordination of the study, performed data analysis and helped to draft the manuscript. All authors read and approved the final manuscript.
In memoriam of Irineu U. Packer.
Irineu U. Packer deceased
Figure S1. Genetic profiling using the Genomic Relationship Matrix. (A). PCA analysis of all 780 Nelore (lineages differentiated by colors). (B). Heatmap and hierarchical clustering of the 780 Nelore. Lateral palette colors represent the families; upper color palette represent the lineages (same color correspondence to A); shades of grey from the heatmap represent relationship similarities (darker is less related). (C). Pedigree view of the families showing the sires (blue), sibs (green), dams (pink) and the lineage ancestral from father side (red). (PDF 1027 kb)
Figure S2. Overall autosomes average r 2 values for Nelore animals with respect to physical genomic distance (kb) and its confidence interval (0.05). (PDF 5 kb)
Table S1. Haplotype block summary per autosome (BTA). (XLSX 6 kb)
Figure S3. Haplotype block distributions for autosome chromosomes (BTA) in Nelore cattle. (PDF 296 kb)
Figure S4. Decay of Ne over ten generations. (PDF 82 kb)
Figure S5. QQ-plots from the GWAS results. (A-H) panels show the QQ-plots for: A. Total Carcass Weight (TCW); B. Dressing % (DRE); C. Rib Eye Area (REA); D. Back Fat Thickness (BFT); E. Lightness of Meat (LM); F. Lightness of Fat (LF); G. pH (PH); H. Cooking Loss (CLO). (PDF 302 kb)
Spreadsheet S1. List of genes tagged by significantly associated SNP in common to this report and Tizioto et al. 2013. (XLSX 16 kb)
Spreadsheet S2. Genes found enriched according to GOrilla. Genes present in the GO:0007155 (“cell adhesion”); GO:0022610 (“biological adhesion”) and GO:0048589 (“developmental growth”), after running GOrilla using an ordered list of genes after a pleiotropy test. (XLSX 14 kb)
Spreadsheet S3. AWM populated with SNP additive effects and p-values (4047 entries). Also genes assigned to each SNP in symbol and ENSEMBL format. (XLSX 747 kb)
Figure S6. Heatmap and hierarchical plot of the AWM/PCIT matrix. Hierarchical plot using the AWM/PCIT correlation matrix (standardized values) for the eight traits. Total Carcass Weight (TCW); Dressing % (DRE); Rib Eye Area (REA); Back Fat Thickness (BFT); Lightness of Meat (LM); Lightness of Fat (LF); pH (PH); Cooking Loss (CLO). (PDF 113 kb)
Figure S7. The fluctuation of heterozygosity along the 224,969 tagSNPs. Red line shows smoothed dataset (one point every 100 tagSNPs). (PDF 269 kb)
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Mudadu, M.A., Porto-Neto, L.R., Mokry, F.B. et al. Genomic structure and marker-derived gene networks for growth and meat quality traits of Brazilian Nelore beef cattle. BMC Genomics 17, 235 (2016). https://doi.org/10.1186/s12864-016-2535-3