Genetic parameters and genome-wide association study of hyperpigmentation of the visceral peritoneum in chickens
- Chenglong Luo†1, 3,
- Hao Qu†1, 3,
- Jie Wang1, 3,
- Yan Wang1, 3,
- Jie Ma1, 3,
- Chunyu Li1, 3,
- Chunfen Yang1, 3,
- Xiaoxiang Hu2,
- Ning Li2 and
- Dingming Shu1, 3Email author
© Luo et al.; licensee BioMed Central Ltd. 2013
Received: 1 February 2013
Accepted: 7 May 2013
Published: 16 May 2013
Hyperpigmentation of the visceral peritoneum (HVP) has recently garnered much attention in the poultry industry because of the possible risk to the health of affected animals and the damage it causes to the appearance of commercial chicken carcasses. However, the heritable characters of HVP remain unclear. The objective of this study was to investigate the genetic parameters of HVP by genome-wide association study (GWAS) in chickens.
HVP was found to be influenced by genetic factors, with a heritability score of 0.33. HVP had positive genetic correlations with growth and carcass traits, such as leg muscle weight (rg = 0.34), but had negative genetic correlations with immune traits, such as the antibody response to Newcastle disease virus (rg = −0.42). The GWAS for HVP using 39,833 single nucleotide polymorphisms indicated the genetic factors associated with HVP displayed an additive effect rather than a dominance effect. In addition, we determined that three genomic regions, involving the 50.5–54.0 Mb region of chicken (Gallus gallus) chromosome 1 (GGA1), the 58.5–60.5 Mb region of GGA1, and the 10.5–12.0 Mb region of GGA20, were strongly associated (P < 6.28 × 10-7) with HVP in chickens. Variants in these regions explained >50% of additive genetic variance for HVP. This study also confirmed that expression of BMP7, which codes for a bone morphogenetic protein and is located in one of the candidate regions, was significantly higher in the visceral peritoneum of Huiyang Beard chickens with HVP than in that of chickens without pigmentation (P < 0.05).
HVP is a quantitative trait with moderate heritability. Genomic variants resulting in HVP were identified on GGA1 and GGA20, and expression of the BMP7 gene appears to be upregulated in HVP-affected chickens. Findings from this study should be used as a basis for further functional validation of candidate genes involved in HVP.
The development of molecular tools and strategies has allowed the investigation of the genetic basis of HVP. Genome-wide association studies (GWAS) have become an important strategy for investigating the genetic basis of many human diseases, including diabetes, breast cancer, pancreatic cancer, and hypertension, amongst others (http://www.genome.gov/GWAStudies). Livestock breeders have begun to implement GWAS to map economically important quantitative trait loci (QTLs) [19–22]. Significant loci linked to chicken growth traits have been mapped to GGA1 and GGA4 by GWAS [23, 24]. Therefore, if HVP is influenced by a major genetic factor, GWAS may be able to dissect its genetic basis.
In this study, we estimated the genetic parameters of HVP to illustrate the inheritance of HVP, and carried out a GWAS analysis of HVP using the chicken 60K single nucleotide polymorphism (SNP) panel in a commercial chicken population with a rich diversity of HVP.
Genetic correlations (r g ) between the hyperpigmentation of visceral peritoneum and growth, carcass, and immune traits in chickens
2,100 ± 16.5
0.27 ± 0.14
2.43 × 10-2
1,847 ± 14.5
0.24 ± 0.14
4.83 × 10-2
1,401 ± 11.7
0.27 ± 0.13
1.86 × 10-2
1,674 ± 13.7
0.21 ± 0.16
9.47 × 10-2
122 ± 1.09
0.17 ± 0.10
3.84 × 10-2
168 ± 1.95
0.34 ± 0.10
4.50 × 10-4
82.6 ± 1.58
0.07 ± 0.12
2.72 × 10-1
129 ± 0.59
−0.06 ± 0.10
2.66 × 10-1
3.63 ± 0.07
−0.42 ± 0.14
1.35 × 10-3
1.31 ± 0.05
−0.26 ± 0.16
5.21 × 10-2
13.4 ± 0.38
−0.25 ± 0.18
8.24 × 10-2
GWAS detection of SNPs associated with HVP
SNPs with statistical significance in the genome-wide association study for hyperpigmentation of visceral peritoneum (HVP)
0.5 Kb U MAP3K7IP1
2.65 × 10-14
2.95 × 10-12
9.03 × 10-12
70.8 Kb U MYH9
1.03 × 10-11
13.3 Kb D MAP3K7IP1
5.07 × 10-11
0.8 Kb U RANGAP1
5.80 × 10-11
1.97 × 10-10
4.62 × 10-9
2.5 Kb D ACO2
5.75 × 10-9
1.52 × 10-8
5.6 Kb U TRIOBP
4.74 × 10-8
55.3 Kb U HIPK2
1.55 × 10-7
2.37 × 10-7
4.85 × 10-7
5.79 × 10-7
30.0 Kb D BMP7
2.44 × 10-8
36.9 Kb U STX16
9.25 × 10-8
1.24 × 10-7
3.5 Kb U RBM38
2.59 × 10-7
27.0 Kb D TFAP2C
3.98 × 10-7
Positional candidate genes for HVP
As shown in the Table 2, there were 18 genes in close proximity to the 20 significant genome-wide SNP markers. The most significant effect was observed in the promoter region (about 0.5 Kb upstream) of TGF-β activated kinase 1/MAP3K7 binding protein 1 (MAP3K7IP1), located in the 50.5–54.0 Mb region of GGA1. Another SNP, located 13.3 Kb downstream of MAP3K7IP1, also had a genome-wide significant additive effect for HVP. Because HVP was associated with immune traits (Table 1), and because MAP3K7IP1 is involved in some pathways associated with energy metabolism and immunity, such as the MAPK signaling pathway and the Toll-like receptor signaling pathway, MAP3K7IP1 was identified as a potential positional candidate gene for HVP. The most significant effect of the other QTLs linked to HVP on GGA1 was at 55.3 kb upstream of the homeodomain interacting protein kinase 2 (HIPK2) locus. HIPK2 participates in cell development, growth, and apoptosis, such as in the Wnt pathway, and was associated with HVP and chicken growth (Table 1), so was therefore also identified as a candidate gene for HVP. The most significant SNP on GGA20 was located nearest to bone morphogenetic protein 7 (BMP7), which can effect melanocyte growth and melanoma cell metastasis, and therefore BMP7 was also chosen as one of the most important positional candidate genes for HVP. In addition, according to information from the Kyoto Encyclopedia of Genes and Genomes (KEGG), Gene Map Annotator and Pathway Profiler (GenMAPP), and Biocarta databases, MAP3K7IP1, HIPK2, and BMP7 can all regulate mitogen-activated protein kinase kinase kinase 7 (MAP3K7) expression (Additional file 2: Figure S2), suggesting that each of these genes might affect HVP by mediating MAP3K7 expression.
Expression of chicken MAP3K7IP1, HIPK2, BMP7, and MAP3K7
Interestingly, chickens with HVP showed no reduction in body weight, and were actually associated with improved production efficiency. This finding deviated from our hypothesis that HVP was likely associated with disease phenotypes, which could decrease chicken growth. However, HVP-affected birds still had greater health risks because of the observed negative genetic correlations with immune traits (Table 1). The birds with HVP had decreased antibody responses, indicating that they may be more likely to suffer from pathogen infections. In addition, the birds with HVP had larger heterophil counts, resulting in higher heterophil to lymphocyte ratios (H/L). High H/L values in chickens are associated with decreased tolerance of environmental stress . Taken together, our results indicated that birds with HVP should grow faster in a favorable environment, but stressful environmental conditions would more adversely affect the development and growth of birds with HVP compared with those of normal birds. We therefore inferred that the increased emergence of birds with HVP indirectly results from the selection of birds with higher production efficiency in the modern broiler industry.
During our investigation of HVP in chickens, we did not observe this HVP phenomenon in fast-growing birds with white feathers, such as Ross 308 broilers; HVP appeared to be limited to colored chicken breeds, such as Huiyang Beard chickens (unpublished data). The lack of the HVP phenotype in Ross 308 broilers may result from interference of the white dominance or recessive locus with the pigmentation in the abdominal septa of areolar connective tissues. A white recessive locus with a retroviral insertion in the tyrosinase (TYR) gene changes the expression of TYR to interrupt melanin biosynthesis [11, 26, 27], while a white dominance locus with a mutation in the premelanosome protein gene alters melanosome shape to influence pigmentation [10, 28]. In addition, birds with runting and stunting syndrome (RSS) usually also have the HVP phenotype in Chinese farms (personal communication). One of reasons behind RSS may be the fact that birds with HVP have less resistance to pathogens and environmental stress, such as cold temperatures. Therefore, HVP may be one of the traits that mirror non-balance allocation of energy between production and immunity during chicken growth. However, this hypothesis required further experimental validation.
A GWAS was implemented for HVP in this study to attempt to validate the above hypotheses. GWAS are useful for exploring the genetic basis of some special appearance traits, such as pigmentation [29, 30]. This was the first study aimed at uncovering the genetic basis of pigmentation of connective tissues in chickens based on a high-density SNP chip panel. We hoped that the findings would increase the genetic knowledge of HVP, and allow us to validate potential HVP candidate genes.
The GWAS identified 20 SNP markers that were significantly (P < 6.28 × 10-7) associated with HVP (Table 2). Based on the extent of LD on GGA1 (Additional file 1: Figure S1), these SNP markers were determined to belong to three different QTLs. The detection of more than one QTL indicates that the causal genes or mutations in these QTLs can affect the same pathway or gene to generate the same phenotype. The MAP3K7IP1, HIPK2, and BMP7 genes were the closest loci to the most significant SNP marker in each of the three QTL regions. MAP3K7IP1, HIPK2, and BMP7 genes are not traditional pigmentation genes, which are generally considered to include MC1R, TYR, tyrosinase-related protein 1, microphthalmia-associated transcription factor (MITF), agouti signaling protein, SRY (sex determining region Y)-box 10 (SOX10), myosin VA (heavy chain 12, myoxin), solute carrier family 45, and member 2 [8, 31, 32]. Therefore, we hypothesized that HVP does not directly result from mutations in the traditional pigmentation genes, but originates from the upstream genes that can indirectly change pigmentation pathways. GWAS of human pigmentation traits have produced some similar results . Previous studies also suggested that MAP3K7IP1, HIPK2, and BMP7 could influence some pigmentation pathways. For example, Liang et al. found that down-regulation of HIPK2 expression suppressed the expression of MITF, resulting in melanocyte differentiation suppression by increasing C-terminal binding protein 2 levels . BMP7 could inhibit normal melanocyte growth and tumor growth of human uveal melanomas [35, 36], and could inhibit metastasis by inducing mesenchymal-to-epithelial transition in melanoma cells . However, evidence indicates that BMP7 is upregulated in the development of melanoma [38, 39]. This study also found that upregulation of BMP7 was associated with HVP in Huiyang Beard chickens (Figure 3). In addition, BMP7 could affect pheomelanin generation by interacting with proopiomelanocortin in brown adipocyte differentiation and thermogenesis [32, 40].
More interestingly, the MAP3K7 gene was found to be a node linking the MAP3K7IP1, HIPK2, and BMP7 genes according to the pathway maps involving these genes in the KEGG, GenMAPP, and BioCarta databases (Additional file 2: Figure S2). MAP3K7 can also interact with many genes affecting melanocyte development [31, 32], such as MITF , KIT ligand, B-cell leukemia/lymphoma 2 [42, 43], lymphoid enhancer binding factor 1 , and epidermal growth factor receptor [45, 46]. MAP3K7IP1 is one of the MAP3K7 binding proteins. The MAP3K7IP1 protein interacts with and thus activates MAP3K7 kinase, and may also function as a mediator between TGF-β receptors and MAP3K7 [47–49], suggesting that MAP3K7IP1 can influence the function of the downstream genes of the pathways involving in MAP3K7. Besides the interaction of MAP3K7IP1 and MAP3K7, BMP7 also contacts MAP3K7 in some pathways. Yamaguchi et al. reported that BMP7 activated MAPK signaling through MAP3K7 . Blank et al. verified that BMP7 activated the JNK signaling pathway, and MAP3K7 was required for BMP7-mediated JNK activation . In addition, BMP7 could activate MAP3K7 and enhance Wnt-dependent transcription . Expression of BMP7 was indeed consistent with that of MAP3K7 in this study (Figure 3). It is possible that a specific mutation upregulates expression of BMP7 to result in MAP3K7 upregulation in Huiyang Beard chickens with HVP. Additionally, the MAP3K7-HIPK2 pathway can inhibit c-Myb activity upon Wnt-1 stimulation, affecting the immune response, because c-Myb plays an essential role in the proliferation of immature hematopoietic cells and early T-cell development [53–55]. This is consistent with the fact that this study identified a strong genetic relationship between HVP and the antibody response to Newcastle disease virus (rg = −0.42, Table 1). Importantly, MAP3K7 participates in several pathways related to the immune response, such as the B cell receptor signaling pathway, the toll-like receptor signaling pathway and the IL-6 signaling pathway (http://www.wikipathways.org/index.php/WikiPathways). These findings indicate that MAP3K7IP1, HIPK2, and BMP7 could be candidate genes for HVP, and might affect the development of HVP by regulating the expression of the MAP3K7 gene. Further studies are needed to validate this hypothesis.
HVP was found to be a quantitative trait with moderate heritability. Three independent QTLs for HVP were detected by GWAS on GGA1 and GGA20, and the BMP7 gene was identified as a likely candidate gene for HVP.
This study was approved by the Animal Care Committee of the Institute of Animal Science, Guangdong Academy of Agricultural Sciences (Guangzhou, People’s Republic of China), with approval number GAAS-IAS-2009-73. Animals involved in this study were humanely sacrificed as necessary to ameliorate their suffering.
Animals and data collection
A total of 585 commercial chickens were used in this study, consisting of three generations (23 P, 51 F1, and 511 F2 individuals) with an accurate pedigree. All birds were immunized with a commercial avian influenza-inactivated H9 strain vaccine at day 40, and a commercial Newcastle disease virus live LaSota strain vaccine at day 50. At day 91, 511 F2 individuals from six hatches were slaughtered. At this time point, vein blood was collected and a portion transferred into centrifuge tubes containing ethylenediaminetetraacetic acid disodium salt solution, and then stored at −80°C. The remainder was used to prepare serum for measuring antibody responses (S/P values) to Newcastle disease virus and avian influenza virus by enzyme linked immunosorbent assay. At day 91, body weight, carcass weight, net weight, dress weight, breast muscle weight, leg muscle weight, and abdomen fat weight were measured, as was small intestine length. Heterophil count, representing H/L, was measured following the method of Vleck et al. . A higher heterophil count is consistent with a higher H/L value. Because HVP was thought to be a quantitative trait, HVP was classified into three levels, absent, mild, and severe hyperpigmentation, represented by 0, 1, and 2 (Figure 1), respectively, to control for false positives. The absent, mild, and severe hyperpigmentation groups had 352, 132, and 27 individuals, respectively.
SNP genotyping and selection
Genomic DNA extraction from venous blood was performed using the phenol/chloroform method. The quality and concentration of genomic DNA from 511 F2 individuals fulfilled the requirements for the Illumina Infinium SNP genotyping platform. Genotyping using the Illumina 60K Chicken SNP Beadchip  was carried out at the Illumina-certified service provider, DNA LandMarks, Saint-Jean-sur-Richelieu, Canada. Quality control was assessed in GenomeStudio v2008.1 . Six samples were excluded as more than 5% of their SNPs had missing genotypes. The final SNP set included 39,833 SNPs for this GWAS under the following SNP selection criteria: low call frequency (>95%), low heterozygosity cluster intensity and separation value (>0.4), and low minor allele frequency (>0.1). Information on the SNP markers on each chicken chromosome is summarized in Additional file 3: Table S1.
Sequences of primers used for qRT-PCR
Forward primers (5′–3′)
Reverse primers (5′–3′)
where y was the vector of observations of HVP, e.g. body weight at day 91(a total of nine phenotypes, Table 1); b was the vector of fixed effects, including sex (two levels) and hatch (six levels); a was the vector of animal additive genetic effects; e was the vector of random residuals; and X and Z were corresponding incidence matrices.
where Y was the phenotypic value of HVP, μ was the common mean of HVP, S was the fixed gender effect, H was the fixed hatch effect, f was the random family effect, SNP was the single-locus SNP genotypic effect, and e was the random residual. Additive and dominance effects were tested using linear contrasts of the single-locus SNP genotypic effect . The threshold P value of the 5% Bonferroni genome-wide significance was 6.28 × 10-7 (0.05/39833/2), based on the total number of SNP markers and two SNP genotypic effects (additive and dominance effects) in GWAS. Manhattan plots were produced using SNPEVG version 2.1  to demonstrate the overview of SNP effects.
To evaluate the extent of LD and identify potential regions of causal mutation for HVP, pairwise LD, measured by r2 values for the F2 population, was calculated for GGA1 and GGA20 using Haploview . Pathway analysis was performed using KEGG (http://www.genome.jp/kegg/), GenMAPP (http://genmapp.org/), and BioCarta (http://genmapp.org/) databases.
Differential expression of MAP3K7IP1, HIPK2, BMP7, and MAP3K7 in the visceral peritoneum tissue, between the normal birds and the birds with HVP, was determined using a t-test with SAS 8.0 software (SAS Institute, Cary, NC, USA).
The authors would like to thank Dr Zheya Sheng (College of Biological Science, China Agricultural University, Beijing, China) for her technical assistance in handling the SNP genotyping data and Dr Yang Da (Department of Animal Science, University of Minnesota, Saint Paul, Minnesota, USA) for his technical support with GWAS. This study was supported by grants from the Guangdong Key Scientific and Technological Projects (Grant No. 2011A020201007), the National Natural Science Foundation of China (Grant No. U0831003), and the Earmarked Fund for Modern Agro-industry Technology Research System (nycytx-42).
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