- Research article
- Open Access
GWAS and transcriptional analysis prioritize ITPR1 and CNTN4 for a serum uric acid 3p26 QTL in Mexican Americans
- Geetha Chittoor1, 2,
- Jack W. KentJr3,
- Marcio Almeida4,
- Sobha Puppala3,
- Vidya S. Farook4,
- Shelley A. Cole3,
- Karin Haack3,
- Harald H. H. Göring4,
- Jean W. MacCluer3,
- Joanne E. Curran4,
- Melanie A. Carless3,
- Matthew P. Johnson4,
- Eric K. Moses5,
- Laura Almasy4,
- Michael C. Mahaney4,
- Donna M. Lehman6,
- Ravindranath Duggirala4,
- Anthony G. Comuzzie3,
- John Blangero4 and
- Venkata Saroja Voruganti1, 2Email author
© Chittoor et al. 2016
- Received: 10 August 2015
- Accepted: 16 March 2016
- Published: 2 April 2016
The variation in serum uric acid concentrations is under significant genetic influence. Elevated SUA concentrations have been linked to increased risk for gout, kidney stones, chronic kidney disease, and cardiovascular disease whereas reduced serum uric acid concentrations have been linked to multiple sclerosis, Parkinson’s disease and Alzheimer’s disease. Previously, we identified a novel locus on chromosome 3p26 affecting serum uric acid concentrations in Mexican Americans from San Antonio Family Heart Study. As a follow up, we examined genome-wide single nucleotide polymorphism data in an extended cohort of 1281 Mexican Americans from multigenerational families of the San Antonio Family Heart Study and the San Antonio Family Diabetes/Gallbladder Study. We used a linear regression-based joint linkage/association test under an additive model of allelic effect, while accounting for non-independence among family members via a kinship variance component.
Univariate genetic analysis indicated serum uric acid concentrations to be significant heritable (h 2 = 0.50 ± 0.05, p < 4 × 10−35), and linkage analysis of serum uric acid concentrations confirmed our previous finding of a novel locus on 3p26 (LOD = 4.9, p < 1 × 10−5) in the extended sample. Additionally, we observed strong association of serum uric acid concentrations with variants in following candidate genes in the 3p26 region; inositol 1,4,5-trisphosphate receptor, type 1 (ITPR1), contactin 4 (CNTN4), decapping mRNA 1A (DCP1A); transglutaminase 4 (TGM4) and rho guanine nucleotide exchange factor (GEF) 26 (ARHGEF26) [p < 3 × 10−7; minor allele frequencies ranged between 0.003 and 0.42] and evidence of cis-regulation for ITPR1 transcripts.
Our results confirm the importance of the chromosome 3p26 locus and genetic variants in this region in the regulation of serum uric acid concentrations.
- Joint linkage/association approach
- Family-based study
The end product of purine metabolism in humans and higher order primates is uric acid, which cannot be further broken down because of lack of uricase . Elevated serum uric acid (SUA) levels or hyperuricemia, a metabolic risk factor for gout and cardio-renal diseases, has been increasing in prevalence worldwide [2–8]. As other cardiovascular and renal disease risk factors, hyperuricemia also has a strong genetic basis [9–11]. SUA is a complex trait, and its pattern of inheritance suggests that several genes may influence it. Numerous genome-wide and candidate gene studies have found various genes, mostly uric acid transporters, to be significantly associated with SUA in several populations, such as solute carrier protein 2 family, member 9 (SLC2A9) [12–17], solute carrier protein 22 family, member 11 (SLC22A11), solute carrier protein 17 family members 1 and 3 (SLC17A1, SLC17A3), solute carrier protein 16 family member 9 (SLC16A9) and ATP-binding cassette, subfamily G. member 2 (ABCG2) [18–21].
In a previous linkage study in 632 Mexican Americans of the San Antonio Family Heart Study, we found strong evidence of linkage for SUA concentrations on 3p26 (LOD = 4.2)  and suggestive evidence of association with the positional candidate gene contactin 4 (CNTN4) . Other candidate genes in this region are inositol 1,4,5-trisphosphate receptor, type 1 (ITPR1), decapping mRNA 1A (DCP1A); transglutaminase 4 (TGM4) and rho guanine nucleotide exchange factor (GEF) 26 (ARHGEF26). The one LOD-confidence interval on 3p26 falls within the candidate region for 3p deletion syndrome whose features include developmental delays and mental retardation . In particular, disruption of CNTN4 and ITPR1 seem to contribute to the 3p deletion syndrome phenotype and may have a causal relationship [22, 23]. SUA is also known as a biomarker for neurodegenerative diseases such as dementia, stroke, Parkinson’s disease and multiple sclerosis [24–28].
Given that we previously identified 3p26 quantitative trait locus (QTL) regulating SUA concentrations, a detailed understanding of the genetic architecture of all candidate genes/variants within this 3p region and its association with SUA is crucial. The aim of this study was to assess the association of variants in the chromosome 3p region in an expanded cohort of 1281 Mexican Americans from the San Antonio Family Heart Study (SAFHS) and the San Antonio Family Diabetes/Gallbladder study (SAFDGS).
Descriptive characteristics and heritability estimates of serum uric acid (mg/dl)
Mean ± SD
Mean ± SD
Mean ± SD
h 2 ± SE
46.01 ± 16.21
47.00 ± 15.53
46.64 ± 15.78
Serum uric acid (mg/dl)a
6.68 ± 1.64
5.28 ± 1.35
5.80 ± 1.61
0.50 ± 0.05
3.2 × 10−35
Age, Sex, Age*Sex
Genome-wide joint linkage/Association analysis
Joint linkage-association analysis of serum uric acid (mg/dl) on chromosome 3
Coordinates NCBI36 (bp)
1.3 × 10−10
9.4 × 10−10
8.6 × 10−10
1.9 × 10−10
9.2 × 10−10
2.0 × 10−10
1.8 × 10−8
4.2 × 10−9
2.8 × 10−8
6.6 × 10−9
7.7 × 10−8
9.1 × 10−4
1.8 × 10−7
4.3 × 10−8
1.9 × 10−7
2.9 × 10−3
2.1 × 10−7
1.8 × 10−3
2.1 × 10−7
3.4 × 10−3
2.2 × 10−7
3.0 × 10−3
2.5 × 10−7
5.0 × 10−3
3.3 × 10−7
8.8 × 10−3
3.7 × 10−7
7.7 × 10−3
3.7 × 10−7
6.7 × 10−3
4.4 × 10−7
1.1 × 10−2
Genotype-specific phenotype means of serum uric acid (mg/dl) concentrations for significant and suggestive associations
Genotype-specific phenotype means [Mean (SD)]
Effect sizeb (%)
Genetic analysis of expression levels of genes in the chromosome 3p region
Genome-wide association of ITPR1 transcript levels
Coordinates NCBI36 (bp)
Effect sizee (%)
2.35 × 10−7
9.05 × 10−7
9.12 × 10−7
3.37 × 10−6
1.19 × 10−6
4.37 × 10−6
2.54 × 10−6
8.89 × 10−6
4.22 × 10−6
1.48 × 10−6
4.94 × 10−6
1.72 × 10−6
1.41 × 10−5
3.44 × 10−5
1.61 × 10−5
5.36 × 10−5
1.71 × 10−5
5.70 × 10−5
1.83 × 10−5
6.07 × 10−5
Our results demonstrate the importance of chromosome 3p26 genetic variants in the regulation of SUA concentrations in Mexican Americans. We identified a QTL with significant evidence of linkage on chromosome 3 (LOD = 4.9) for SUA in an expanded cohort, confirming our previous linkage of a novel QTL on chromosome 3p26 affecting SUA and better reflecting pedigree-specific effects. This region has been reported to harbor positional candidate genes with potential relevance to cardiovascular disease, hypertension, obesity, and metabolic syndrome [2–5]. CNTN4, a candidate gene in the linkage region of 3p26, is a member of the contactin subgroup of cell adhesion molecules of the immunoglobulin (Ig) superfamily and plays an important role in maintenance and plasticity of functional neuronal networks and central nervous system (CNS) development . The variants in this gene are associated with developmental delays and mental retardation and may be relevant to autism-related spectrum disorders [30–32]. Disruption of CNTN4 is also thought to cause cognitive defects . Our study showed strong association of SUA concentrations with CNTN4 SNPs. Specifically, one CNTN4 variant, rs9854606 is notable with a minor allele frequency (T) of 0.4 %. Although, SUA has not been associated with autism or related disorders, it has been considered a biomarker for neurological disorders such as Parkinson’s disease , multiple sclerosis  and Alzheimer’s disease [36, 37] and cognitive defects [38, 39].
Other genes in our QTL region, ITPR1, DCP1A and TGM4, do not seem to have functional relevance to SUA concentrations. However, all of these genes are located in or border the ~4.5 Mb region which is associated with a syndrome known as 3p deletion syndrome. Individuals with 3p deletion syndrome have a rare genetic disorder characterized by developmental delay, growth retardation and dysmorphic features . ITPR1 encodes an intracellular IP3-gated calcium channel involved in calcium signaling . Mutations in this gene have been associated with spinocerebellar ataxia  and platelet signaling pathways , and DCP1A is known to play a role in mRNA decay and also in prematurely terminating protein synthesis .
As described in the methods, the JLA approach has the potential to amplify a signal taking into consideration random effects of shared sequence identity (linkage) and the fixed effects of marker genotypes (association), thus maximizing the information in a sample of related individuals . With this approach, we had previously found common SNPs, MAF > 5 %, in SLC2A9 to be significantly associated with SUA levels in Mexican Americans . Our JLA approach also has the ability to detect rare variants which were primarily from the chromosome 3p26 region showing that rare or low frequency variants are more likely to be identified by linkage rather than association. Of the top 6 significant SNPs, 5 of them had MAF ≤ 5 %. Family-based studies provide the best opportunity to identify these rare variants, with Mendelian transmission from parent to offspring offering a chance to maximize copies of rare variants in the pedigree. This was supported by our analyses when we found that about six families contributed the most to the LOD score (~4.6). When we conducted the linkage analysis removing these families, the LOD score was reduced to zero, whereas, linkage analysis in just these families increased the LOD score to 5.5.
The association between SUA concentrations and variants in the chromosome 3p region has not been reported in any population except a study in an isolated population in Europe. This study reported epistasis between SLC2A9 and CNTN4 suggesting a link between SUA levels and autism-related spectrum disorder. Purine metabolism disorders have been reported in autism spectrum disorders [44, 45] particularly hyperuricosuric autism. Adenosine, a precursor of uric acid in purine metabolic pathway, is believed to be neuroprotective and known to promote sleep and reduce seizures  indicating its potential as a therapeutic agent for autism. Lack of replication of the associations between SUA and CNTN4 or ITPR1 SNPs by other studies is a limitation of the study. However, considering the role of purine metabolic disorders in autism, role for CNTN4 and ITPR1 in the regulation of SUA seems plausible and needs to be evaluated further.
To gain further support for the association with the chromosome 3p26 region, we conducted JLA of cis-regulated ITPR1 transcript. Our best associations of these transcript levels were with SNPs in ITPR1 and SCN8A genes. Cis-regulated transcripts contain genetic variation within their gene and regulatory regions that affect their abundance . The SCN8A gene encodes a protein that is important for neuron hyperexcitability  and mutations in this gene are known to cause cerebellar ataxia, which is the similar to that of ITPR1. Given the importance of 3p region in neurological disorders and potential role of uric acid as biomarker for these disorders, this region assumes significance.
Our findings demonstrate the importance of variants in chromosome 3p26 region, particularly SNPs in ITPR1 and CNTN4, in the regulation of SUA concentrations in our cohort. The results of this study are very promising, though further work needs to be performed to validate them.
The San Antonio Family Heart Study (SAFHS) and the San Antonio Family Diabetes/Gallbladder study (SAFDGS): The recruitment for the SAFHS was initiated in 1991, and recruitment for SAFDGS was conducted between 1998 and 2001. Details of study recruitment and related material have been detailed previously [48–51]. Genome-wide association, joint linkage/association, and transcriptional analyses were performed on 1281 individuals, coming from 120 Mexican American families from these two studies, for whom whole genome-wide SNP data and related phenotype data were available.
For both SAFHS and SAFDGS, several metabolic, hemodynamic, anthropometric, and demographic variables were collected using standard procedures [46, 48]. Uric acid was measured in serum by a colorimetric assay using uricase and peroxidase . A description of the measurement techniques is given elsewhere [9, 12, 53]. Uric acid levels were rank-inverse-normalized prior to genetic analysis.
The transcriptional profiling in the SAFHS was performed in 1281 individuals. The methodology related to isolation of lymphocytes from whole blood, isolation of total RNA, anti-RNA synthesis, amplification and purification and identification of expressed transcripts is described in detail in Göring et al., 2007 .
Genome-wide association (GWAS) analysis was conducted in the SAFHS/SAFDGS using SNP genotypes obtained from the Illumina HumanHap550 BeadChip (Illumina, SanDiego, CA). Our experimental error rate (based on duplicates) was 2 per 100,000 genotypes. The average call rate per individual sample was 97 %. Approximately 1 per 1000 genotypes was blanked due to Mendelian errors. Specific SNPs were removed from analysis if they had call rates <95 % (about 4000SNPs) or deviated from Hardy–Weinberg equilibrium at a 5 % false discovery rate (FDR) (12SNPs). Missing genotypes were imputed from pedigree data using MERLIN . SNP genotypes were checked for Mendelian consistency using the program SimWalk2 . The estimates of the allele frequencies and their standard errors were obtained using Sequential Oligogenic Linkage Analysis Routines (SOLAR) .
We used a variance components decomposition-based method in SOLAR to estimate heritability of serum uric acid and transcript levels of associated genes. Total phenotypic variance can be partitioned into its genetic and environmental components. The fraction of total phenotypic variance (V P ) resulting from additive genetic effects (V G ) is called heritability and is denoted as h 2 = V G /V P . All traits were adjusted for age, sex and their interaction effects.
Joint linkage/Association analysis
We used a joint linkage/association (JLA) approach for each SNP, implemented in SOLAR, that tested each saturated model (including linkage and the fixed effect of the SNP) against a null model in which both effects were constrained to zero. All SNPs in the GWAS panel were mapped not only to their physical location but also to their genetic position, given as the nearest integral centiMorgan, based on public data . JLA may improve detection when multiple causal variants are present, as the summed effects of adjacent variants captured by linkage may amplify the fixed effect of each measured marker. A subsidiary measured genotype association analysis (MGA)  tested the additive effect of each SNP genotype conditioned on the genome-wide genetic similarity of the relatives (i.e., a standard GWAS corrected for relatedness). The genome-wide significance threshold p-value was set at p < 3.1 × 10−7 using Bonferroni correction for multiple tests based on the effective number of independent SNPs given linkage disequilibrium (LD) within the sample .
All participants gave written informed consent. Protocol for both studies (SAFHS and SAFDGS) were approved by the Institutional Review Boards at the University of Texas Health Science Center San Antonio and University of North Carolina at Chapel Hill
Major portion of the data used in this study is deposited in dbGAP (T2D-GENES Project 2: San Antonio Mexican American Family Studies.dbGAP Study Accession: phs000462.v1.p1. http://0-www.ncbi.nlm.nih.gov.brum.beds.ac.uk/projects/gap/cgi-bin/study.cgi?study_id=phs000462.v1.p1.
Rest of the data is in the process of being deposited. However, we welcome the opportunity to form formal collaborations with investigators who are working in this research area and are interested in utilizing these data.
We wish to thank all participants for their cooperation and generous participation.
This work was supported by grants R01DK092238, R01 DK047482 and R01 DK053889 from National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK), PO1 HL045522 from National Heart, Lung and Blood Institute (NHLBI) and MH059490 from National Institute of Mental Health (NIMH) of the National Institutes of Health. The SAFHS is supported by P01 HL045522; the SAFDS is supported by R01 DK047482; the SAFGS is supported by R01 DK053889. A donation from the Azar and Shepperd families in San Antonio paid for the SNP typing in the SAFHS. This investigation was conducted in part in facilities constructed with support from the Research Facilities Improvement Program under grant numbers C06 RR013556 and C06 RR017515. The AT&T Genomics computing center supercomputing facilities used for this work were supported in part by a gift from the AT&T Foundation and with support from the National Center for Research Resources Grant Number S10RR029392. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
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