- Research article
- Open Access
Genome-wide association study of copy number variation with lung function identifies a novel signal of association near BANP for forced vital capacity
BMC Genetics volume 17, Article number: 116 (2016)
Genome-wide association studies of Single Nucleotide Polymorphisms (SNPs) have identified 55 SNPs associated with lung function. However, little is known about the effect of copy number variants (CNVs) on lung function, although CNVs represent a significant proportion of human genetic polymorphism. To assess the effect of CNVs on lung function quantitative traits, we measured copy number at 2788 previously characterised, common copy number variable regions in 6 independent cohorts (n = 24,237) using intensity data from SNP genotyping experiments. We developed a pipeline for genome-wide association analysis and meta-analysis of CNV genotypes measured across multiple studies using SNP genotype array intensity data from different platform technologies. We then undertook cohort-level genome-wide association studies of CNV with lung function in a subset of 4 cohorts (n < =12,403) with lung function measurements and meta-analysed the results. Follow-up was undertaken for CNVs which were well tagged by SNPs, in up to 146,871 individuals.
We generated robust copy number calls for 1962 out of 2788 (70 %) known CNV regions genome-wide, with 1103 measured with compatible class frequencies in at least 2 cohorts. We report a novel CNV association (discovery P = 0.0007) with Forced Vital Capacity (FVC) downstream of BANP on chromosome 16 that shows evidence of replication by a tag SNP in two independent studies (replication P = 0.004). In addition, we provide suggestive evidence (discovery P = 0.0002) for a role of complex copy number variation at a previously reported lung function locus, containing the rootletin gene CROCC, that is not tagged by SNPs.
We demonstrate how common CNV regions can be reliably and consistently called across cohorts, using an existing calling algorithm and rigorous quality control steps, using SNP genotyping array intensity data. Although many common biallelic CNV regions were well-tagged by common SNPs, we also identified associations with untagged mulitallelic CNV regions thereby illustrating the potential of our approach to identify some of the missing heritability of complex traits.
Genome-wide association studies (GWAS) of single nucleotide polymorphisms (SNPs) have highlighted genes and biological pathways associated with risk of a variety of diseases and variability in quantitative health-related traits. Quantitative lung function traits are of major public health relevance and large GWAS have identified multiple common variants which collectively explain only a small proportion of the phenotypic variance. For lung function traits (forced expired volume in 1 second, FEV1, forced vital capacity, FVC and the ratio FEV1/FVC), the 55 SNPs reported in recent large GWAS explain 6.6 % of the variance in FEV1/FVC, 5.3 % of the variance in FEV1 and 4.0 % for FVC [1–6].
Copy number variants (CNVs) are deletions or duplications of parts of a chromosome, ranging from a few hundred to a few million base pairs in length , leading to extra or fewer copies of a certain DNA sequence relative to the usual 2 copies for a diploid genome. CNVs have been associated with several disorders including Crohn’s disease, rheumatoid arthritis and diabetes [8, 9] and neurological disorders such as schizophrenia [10, 11], autism [12, 13] and developmental delay , although contribution of CNVs to phenotypic variance is still uncertain for many common traits [9, 15, 16]. To date, no genome-wide survey of the effect(s) of copy-number variants on lung function quantitative traits has been carried out.
Platforms primarily designed for SNP genotyping can additionally provide an estimate of copy number by looking for deviations in the intensity signal from each allelic SNP probe; “non-polymorphic” probes (probes at genomic positions where there is no known SNP) have been added to some GWAS platforms specifically for this purpose. The wide availability of these intensity data presents an opportunity to measure genome-wide copy number variation across multiple studies and bring together large sample sizes for association testing.
Here we describe a pipeline for genome-wide CNV genotype measurement using SNP array intensity data. We first tested the pipeline and defined appropriate quality control filters using 6 cohorts comprising intensity data from 5 different genotyping platforms. We then undertook an analysis of genome-wide CNV associations with lung function for up to 12,403 individuals in a subset of 4 cohorts with lung function measurements at 1962 copy number variable loci. We show how this approach can identify multiallelic variants that are not well-tagged by SNPs and that potentially explain some of the missing heritability of lung function quantitative traits.
There were 2 stages of the analysis. In the first stage we refined a pipeline for copy number calling to determine the quality control steps required to obtain consistent copy number measurement across multiple cohorts and genotyping platforms. In this stage we analysed intensity data from SNP genotyping platform experiments for 24,237 samples from 6 different cohorts (Busselton Health Study (BHS, n = 3496), Young Finns Study (YFS, n = 2682), British 1958 Birth Cohort (B58C, n = 2920), Study of Health in Pomerania (SHIP, n = 4072), Raine Study (n = 1685) and the Avon Longitudinal Study of Parents and Children (ALSPAC, n = 9382)). The aim of this first stage was to identify whether common CNVs could be measured with consistency across multiple cohorts with different intensity data. In the second stage we tested for association of copy number with lung function in 4 cohorts which had lung function measurements. Lung function association results were then meta-analysed across cohorts.
In stage 1 we selected known, common copy number variable regions (CNVRs) from a map of 11,700 copy number variants across the genome published by The Genome Structural Variation Consortium , which included 3276 autosomal CNVRs observed twice or more in 20 HapMap CEU samples. Of these, 2788 CNVRs were retained after quality control (Additional file 1).
The Log R Ratio (LRR) of the intensity signals from the allelic probes used in the SNP genotyping was used to estimate copy number. LRR is the ratio of the intensity to the expected intensity of the relevant genotype cluster and is a transformation of the raw X and Y intensity signals that enhances the correlation with copy number. The LRR was available for all of the cohorts apart from ALSPAC where the sum of the X and Y intensities from each of the allelic probes was used instead. Replicate samples and samples which failed intensity noise filtering (Additional file 1) were excluded before copy number calling. Where SNP genotypes were available, we derived ancestry-informative principal components using EIGENSOFT  and removed any samples that had a score on any of the first 4 principal components greater than 6 standard deviations from the mean.
At each CNVR the samples passing the above quality-control filters were clustered by a 1-dimensional summary of the intensity signals from the probes within the CNVR boundary; only samples with non-missing data for these probes were included when clustering each CNVR. The cluster to which a sample belongs was used as a proxy for the copy number class of the sample at that CNVR. The clustering was performed by Bayesian hierarchical mixture modelling implemented in the R package CNVCALL [9, 19].
For the initial run of clustering no prior information about the number of classes was included, with the algorithm determining the most likely number of classes from the data independently for each cohort. In the absence of a “gold standard” for the correct number of classes at each CNVR, we used the number of classes called by the best-performing cohort as our best estimate of the true number of classes for a CNVR. The best-performing cohort was the cohort in which the clusters were most clearly defined and hence in which the highest number of polymorphic CNVRs could be called. In this way, where the number of classes initially clustered in the first run of the algorithm was different across cohorts, we re-clustered CNVRs, fixing the number of classes to be that obtained in the first run in the best-performing cohort. CNVRs were determined to be high quality if they were called in the best-performing cohort or had class frequencies compatible with the best-performing cohort (Additional file 1).
For stage 2, lung function measurements (FEV1, FVC and FEV1/FVC) were available for 3 adult cohorts (BHS, B58C and SHIP) and 1 child cohort (ALSPAC). We tested for association of FEV1, FVC and FEV1/FVC with CNVR copy number within each cohort and results were then meta-analysed across up to 4 cohorts as the primary analysis and then across up to 3 cohorts of adults to look for age specific effects. Only CNVRs called with the same number of classes and consistent class frequencies across cohorts in stage 1 (Additional file 1) were included in meta-analyses. Uncertainty in copy number assignment due to weakly defined clustering was taken into account in association testing by using copy number dose (Additional file 1) . Association testing for cohorts with unrelated individuals was performed using a linear model of phenotype with copy number dose. Lung function phenotypes were adjusted for age, age2, sex, height and height2 and first 4 ancestry principal components. As there were related individuals in BHS we used a generalised-estimating equation (GEE) to account for correlation within families . A detailed description of the cohorts is given in the Supplementary Material. A flow diagram of the whole pipeline from all initially available samples and CNVRs through to final meta-analysis results is shown in Additional file 1: Figure S1.
For CNVRs which were well-tagged by SNPs (r2 > 0.7), we sought replication of suggestive signals of association (P < 0.001) for lung function in a large GWAS. Linkage disequilibrium (r2) between each CNVR and SNPs within 1 Mb of the CNVR start and end positions was measured using samples in the BHS cohort that had both copy number genotypes and imputed SNP genotypes (1000 Genomes Project Phase 1 imputation reference panel). For replication we used results from the SpiroMeta and CHARGE consortia meta-analysis of 48,201 individuals across 23 studies [3, 4], the UK BiLEVE lung function GWAS  (n = 48,943, Additional file 1) and the subset of samples from the 152,729 UK Biobank samples genotyped at the time of writing that were not in UK BiLEVE and with lung function measurements passing ERS/ATS criteria (n = 49,727, Additional file 1). In the replication studies lung function traits were adjusted for age, age2, sex, height, pack years in smokers where available, and ancestry principal components where available. Residuals were inverse rank inverse-normal transformed after adjustment apart from FVC in SpiroMeta and CHARGE, which was untransformed , hence for FEV1 and FEV1/FVC we used inverse-variance weighted meta-analysis across the replication cohorts and for FVC we used Z-score meta-analysis. All replication resources were comprised of European ancestry individuals. For replication, we used a Bonferroni corrected 5 % threshold for the number of CNVRs with a tag SNP available. Replication was not available for CNVRs not well-tagged by SNPs (r2 > 0.7).
We tested for enrichment of gene ontology (GO) terms using DAVID [http://david.abcc.ncifcrf.gov/] within genes spanned by CNVRs showing association with P < 0.01 for our lung function traits in the meta-analysis of all cohorts and separately within the meta-analysis of adult and child cohorts. We used a Bonferroni correction for all GO terms showing nominal significance of P < 0.05. We used GTEx to perform a look up of eQTL signals of SNPs tagging CNVRs using an empirical 5 % threshold determined by permutation by GTEx.
For the first stage of the analysis, aimed at developing a pipeline for copy number calling across different genotyping platforms, intensity data was available for 24,259 samples from 6 cohorts. After filtering, 19,308 samples were taken forward for CNVR clustering and copy number calling. The total number of CNVRs called and the proportions of deletions, amplifications and multiallelic CNVRs called in each cohort varied across genotyping platforms (Table 1) and hence we only meta-analysed CNVRs that were called consistently across platforms. As CNVCALL was able to resolve the largest proportion of the 2788 CNVRs as polymorphic in the BHS cohort data (1962 CNVRs, 70.4 %) and the clustering gave the best separation of classes in the BHS data (Additional file 1), the number of classes called in the BHS cohort was used as our best estimate of the true number of classes and as the standard for calling CNV genotypes with a consistent number of classes across all cohorts. The numbers of CNVRs initially clustered in the 6 cohorts are shown in Table 1 and the overlap of clustered CNVRs across cohorts is shown in Additional file 1: Figure S2. Differences in the numbers of CNVRs successfully clustered in each cohort could be due to differences in data quality, differences in probe content on different genotyping platforms or the available intensity measures (LRR vs X + Y). 1103 CNVRs could be clustered with number of classes and class frequencies compatible with BHS (χ2 test described in Additional file 1) in at least 1 other cohort. This filtered set of CNVRs was enriched for deletions in all cohorts compared to the initial set (Table 1).
For the second stage of the analysis, lung function data was available for 19,870 samples from 4 cohorts. After filtering, 12,403 samples were taken forward for association testing (Table 2). None of our CNVR associations reached a 5 % Bonferonni threshold for 1962 independent tests (P < 2.5 × 10-5); the full set of association results are provided in Additional file 2. We sought replication of suggestive associations (P < 0.001) which included 12 CNVR-trait combinations (11 distinct CNVRs) in the adult cohorts analysis (Table 3; Quantile-Quantile and Manhattan plots are in Additional file 1: Figure S4 and Figure S5).
Replication was sought for these 12 CNVR associations by looking at association of SNPs tagging the CNVR in independent cohorts (Table 3). Out of 12 CNVR-trait combinations showing suggestive evidence of association with lung function, (P < 0.001), 7 (including CNVR4222.1 which was associated with both FEV1 and FVC; Table 3) were well tagged by a 1000G SNP (r2 > 0.7). A SNP tagging CNVR6854.1 (rs7501378, r2 = 0.94) showed replication of association with FVC in UK BiLEVE and in the meta-analysis of the 3 replication cohorts (Table 3) using a Bonferroni-corrected 5 % threshold for 8 tests (P < 0.006). The direction of effect of this CNVR was consistent across the 3 discovery CNVR cohorts and was in the same direction in SpiroMeta, CHARGE and UK BiLEVE for the SNP allele positively correlated with increased copy number, but in the opposite direction in the non-significant UK Biobank association (Table 3). CNVR6854.1 is located at 16q24.2 and is 2.0 kb downstream of BANP (BTG3 Associated Nuclear Protein, also known as Scaffold/Matrix-Associated Region-1-Binding Protein [SMAR1]). The tag SNP rs7501378 is 420 bp further downstream of BANP than CNVR6854.1 (Additional file 1: Figure S6). There was no evidence for this SNP as an eQTL in blood [23, 24] or lung .
The 3 strongest signals of association with lung function in the discovery meta-analysis (FEV1/FVC, P = 1.96-2.69 × 10-4, CNVR94.3, CNVR94.4 and CNVR94.5) were for 3 overlapping and correlated CNVRs within or near to CROCC, a gene that encodes rootletin, a component of cilia (Additional file 1: Figure S7). CNV94.3 was measured as a 3 class CNV in a previous study  and showed consistent class frequencies with those observed in BHS and B58C (Additional file 1: Table S1). However, no tagging SNP was available.
Across the 45 genes implicated by CNVRs showing nominal evidence of association (P < 0.01) with lung function in this study, no enrichment of gene ontology terms was seen (P < 0.05).
We developed a quality-control pipeline for genome-wide association analysis and meta-analysis of CNV genotypes and generated robust copy number calls across cohorts for 1962 CNVs genome-wide across 6 cohorts comprising 5 different genotyping platforms. Of these, 1103 CNVs could be clustered consistently in at least 2 cohorts, 777 in 3 cohorts, 371 in 4 cohorts and 70 in 5 cohorts. No CNVRs could be clustered across all 6 cohorts (Additional file 1: Figure S2). We tested for association of each CNVR with lung function in a subset of 4 cohorts and then undertook meta-analyses for adults and children combined and adults only. A signal of association with FVC for a CNVR downsream of BANP on chromosome 16 was replicated using a tag SNP in 2 large independent studies. The class frequencies of this CNVR observed in our study were consistent with those previously measured  providing reassurance that this CNVR has been measured accurately. BANP is expressed in a range of organ tissues including respiratory epithelial cells [http://www.proteinatlas.org/] and has been shown to have a role in regulation of alternative splicing via a histone deactylase 6 (HDAC6)-mediated deactylation pathway [25, 26] (other HDACs, including HDAC6, have previously been implicated in chronic obstructive pulmonary disease (COPD) and lung function [27, 28]).
An additional five CNVRs which showed suggestive evidence of association with lung function in our study were complex (i.e. did not have 3 copy number classes) and hence not well tagged by bi-allellic 1000G SNPs. Amongst these were 3 correlated CNVRs which had the strongest evidence of association for FEV1/FVC (P = 2.0-2.7 × 10-4) and which involved the CROCC gene in a region that has previously been shown to be associated with lung function . These 3 CNVRs are not tagged (r2 = 0.005) by the previously reported SNP showing strong evidence of association with FEV1/FVC (rs2284746, P = 7.5x10-16), which is within 25 kb . Collectively, these 3 CNVRs would explain an additional 0.46 % of the variance in FEV1/FVC in addition to the 3.2 % of variance in FEV1/FVC already accounted for by genome-wide significantly associated SNPs . It has been shown in Crocc knockout mice that loss of rootletin (the protein encoded by Crocc) prevents the formation of the ciliary rootlet in airway epithelial cells leading to a reduction in motile cilium function with pathological changes consistent with insufficient mucociliary clearance . CROCC is in a region which is annotated as containing several overlapping CNVRs  (Additional file 1: Figure S7); however some nested CNVRs could actually be the result of incomplete measurement of the larger CNVR within which they are found. The preliminary CNV associations in CROCC warrant further verification. Determining the precise genomic architecture of the region is needed to understand the nature of the associations observed in this study.
Meta-analysis of association test statistics from multiple cohorts is a routine approach to increase sample sizes in GWAS based on SNP data when individual-level data cannot be analysed all together. SNPs that are assayed on commercial platforms are biallelic and well characterised in terms of expected allele frequencies and the assays themselves are designed to accurately measure SNP genotypes. In contrast, CNVRs are less well-characterised and although the use of SNP genotyping platform intensity presents a useful and economical approach to measure copy number variation, this also presents challenges. In this study, we presented a pipeline for ensuring compatibility of CNV genotypes before meta-analysis when these have been derived from different data sources (both in terms of platform and probe set). We were able to generate compatible copy number calls across at least 2 cohorts for over one thousand CNVRs genome-wide. Differences in concordance of CNV class frequencies between pairs of cohorts with SNP genotyping data from the same or similar versions of Illumina platforms could be due to differences in intensity data quality. It was evident that older versions of the platforms had poorer probe coverage of the CNVRs than the more recent platforms, some of which had content designed specifically for the larger set of CNVRs from which the subset analysed here were selected. We chose to use the number of copy number classes and class frequencies from one cohort as the best estimate of the true number of classes to which other cohorts were compared with validation of the genotypes measured in this reference cohort against CNV genotypes in an independent cohort. As new cohorts emerge and existing cohorts update their genotype data using newer arrays, compatibility across cohorts for increasing numbers of CNVRs is likely to increase.
We demonstrate how common CNV regions can be reliably and consistently called across cohorts, using an existing calling algorithm and rigorous quality control steps, using SNP genotyping array intensity data. Using this approach, we describe a novel signal of association with FVC for a copy number variable locus downstream of BANP on chromosome 16 and present evidence that copy number variation may play a role at a locus previously reported as being associated with lung function (CROCC).
1000G, 1000 genomes project; ALSPAC, avon longitudinal study of parents and children; B58C, British 1958 birth cohort; BHS, busselton health study; CHARGE, cohorts for heart and aging research in genomic epidemiology; CNV, copy number variant; CNVR, copy number variable region; ERS/ATS, european respiratory society / american thoracic society; FEV1, forced expiratory volume in 1 second; FVC, forced vital capacity; GWAS, genome-wide association study; LRR, Log R ratio; SHIP, study of health in pomerania; SNP, single nucleotide polymorphism; UK BiLEVE, UK biobank lung exome Variant Evaluation; YFS, young finns study
Repapi E, Sayers I, Wain LV, Burton PR, Johnson T, Obeidat M, Zhao JH, Ramasamy A, Zhai G, Vitart V, Huffman JE, Igl W, Albrecht E, Deloukas P, Henderson J, Granell R, McArdle WL, Rudnicka AR, Barroso I, Loos RJF, Wareham NJ, Mustelin L, Rantanen T, Surakka I, Imboden M, Wichmann HE, Grkovic I, Jankovic S, Zgaga L, Hartikainen A-L, et al. Genome-wide association study identifies five loci associated with lung function. Nat Genet. 2010;42:36–44.
Hancock DB, Eijgelsheim M, Wilk JB, Gharib SA, Loehr LR, Marciante KD, Franceschini N, van Durme YMTA, Chen T, Barr RG, Schabath MB, Couper DJ, Brusselle GG, Psaty BM, van Duijn CM, Rotter JI, Uitterlinden AG, Hofman A, Punjabi NM, Rivadeneira F, Morrison AC, Enright PL, North KE, Heckbert SR, Lumley T, Stricker BHC, O’Connor GT, London SJ. Meta-analyses of genome-wide association studies identify multiple loci associated with pulmonary function. Nat Genet. 2010;42:45–52.
Soler Artigas M, Loth DW, Wain LV, Gharib SA, Obeidat M, Tang W, Zhai G, Zhao JH, Smith AV, Huffman JE, Albrecht E, Jackson CM, Evans DM, Cadby G, Fornage M, Manichaikul A, Lopez LM, Johnson T, Aldrich MC, Aspelund T, Barroso I, Campbell H, Cassano PA, Couper DJ, Eiriksdottir G, Franceschini N, Garcia M, Gieger C, Gislason GK, Grkovic I, et al. Genome-wide association and large-scale follow up identifies 16 new loci influencing lung function. Nat Genet. 2011;43:1082–90.
Loth DW, Soler Artigas M, Gharib SA, Wain LV, Franceschini N, Koch B, Pottinger TD, Smith AV, Duan Q, Oldmeadow C, Lee MK, Strachan DP, James AL, Huffman JE, Vitart V, Ramasamy A, Wareham NJ, Kaprio J, Wang X-Q, Trochet H, Kahonen M, Flexeder C, Albrecht E, Lopez LM, de Jong K, Thyagarajan B, Alves AC, Enroth S, Omenaas E, Joshi PK, et al. Genome-wide association analysis identifies six new loci associated with forced vital capacity. Nat Genet. 2014;46:669–77.
Soler Artigas M, Wain LV, Miller S, Kheirallah AK, Huffman JE, Ntalla I, Shrine N, Obeidat M, Trochet H, McArdle WL, Alves AC, Hui J, Zhao JH, Joshi PK, Teumer A, Albrecht E, Imboden M, Rawal R, Lopez LM, Marten J, Enroth S, Surakka I, Polasek O, Lyytikainen L-P, Granell R, Hysi PG, Flexeder C, Mahajan A, Beilby J, Bosse Y, et al. Sixteen new lung function signals identified through 1000 Genomes Project reference panel imputation. Nat Commun. 2015;6:8658.
Wain LV, Shrine N, Miller S, Jackson VE, Ntalla I, Soler Artigas M, Billington CK, Kheirallah AK, Allen R, Cook JP, Probert K, Obeidat M, Bossé Y, Hao K, Postma DS, Paré PD, Ramasamy A, Mägi R, Mihailov E, Reinmaa E, Melén E, O’Connell J, Frangou E, Delaneau O, Freeman C, Petkova D, McCarthy M, Sayers I, Deloukas P, Hubbard R, et al. Novel insights into the genetics of smoking behaviour, lung function, and chronic obstructive pulmonary disease (UK BiLEVE): a genetic association study in UK Biobank. Lancet Respir Med. 2015;3:769–81.
Wain LV, Armour JA, Tobin MD. Genomic copy number variation, human health, and disease. Lancet. 2009;374:340–50.
McCarroll SA, Huett A, Kuballa P, Chilewski SD, Landry A, Goyette P, Zody MC, Hall JL, Brant SR, Cho JH, Duerr RH, Silverberg MS, Taylor KD, Rioux JD, Altshuler D, Daly MJ, Xavier RJ. Deletion polymorphism upstream of IRGM associated with altered IRGM expression and Crohn’s disease. Nat Genet. 2008;40:1107–12.
Craddock N, Hurles ME, Cardin N, Pearson RD, Plagnol V, Robson S, Vukcevic D, Barnes C, Conrad DF, Giannoulatou E. Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls. Nature. 2010;464:713–20.
Xu B, Roos JL, Levy S, van Rensburg EJ, Gogos JA, Karayiorgou M. Strong association of de novo copy number mutations with sporadic schizophrenia. Nat Genet. 2008;40:880–5.
Ruderfer DM, Chambert K, Moran J, Talkowski M, Chen ES, Gigek C, Gusella JF, Blackwood DH, Corvin A, Gurling HM, Hultman CM, Kirov G, Magnusson P, O’Donovan MC, Owen MJ, Pato C, St Clair D, Sullivan PF, Purcell SM, Sklar P, Ernst C. Mosaic copy number variation in schizophrenia. Eur J Hum Genet. 2013;21:1007–11.
Sebat J, Lakshmi B, Malhotra D, Troge J, Lese-Martin C, Walsh T, Yamrom B, Yoon S, Krasnitz A, Kendall J, Leotta A, Pai D, Zhang R, Lee Y-H, Hicks J, Spence SJ, Lee AT, Puura K, Lehtimaki T, Ledbetter D, Gregersen PK, Bregman J, Sutcliffe JS, Jobanputra V, Chung W, Warburton D, King M-C, Skuse D, Geschwind DH, Gilliam TC, et al. Strong Association of De Novo Copy Number Mutations with Autism. Science. 2007;316:445–9.
Girirajan S, Dennis MY, Baker C, Malig M, Coe BP, Campbell CD, Mark K, Vu TH, Alkan C, Cheng Z, Biesecker LG, Bernier R, Eichler EE. Refinement and Discovery of New Hotspots of Copy-Number Variation Associated with Autism Spectrum Disorder. Am J Hum Genet. 2013;92:221–37.
Coe BP, Witherspoon K, Rosenfeld JA, van Bon BWM, Vulto-van Silfhout AT, Bosco P, Friend KL, Baker C, Buono S, Vissers LELM, Schuurs-Hoeijmakers JH, Hoischen A, Pfundt R, Krumm N, Carvill GL, Li D, Amaral D, Brown N, Lockhart PJ, Scheffer IE, Alberti A, Shaw M, Pettinato R, Tervo R, de Leeuw N, Reijnders MRF, Torchia BS, Peeters H, Thompson E, O’Roak BJ, et al. Refining analyses of copy number variation identifies specific genes associated with developmental delay. Nat Genet. 2014;46:1063–71.
Chen X, Li X, Wang P, Liu Y, Zhang Z, Zhao G, Xu H, Zhu J, Qin X, Chen S, Hu L, Kong X. Novel Association Strategy with Copy Number Variation for Identifying New Risk Loci of Human Diseases. PLoS One. 2010;5:e12185.
Marques F, Prestes P, Pinheiro L, Scurrah K, Emslie K, Tomaszewski M, Harrap S, Charchar F. Measurement of absolute copy number variation reveals association with essential hypertension. BMC Med Genomics. 2014;7:44.
Conrad DF, Pinto D, Redon R, Feuk L, Gokcumen O, Zhang Y, Aerts J, Andrews TD, Barnes C, Campbell P, Fitzgerald T, Hu M, Ihm CH, Kristiansson K, MacArthur DG, MacDonald JR, Onyiah I, Pang AWC, Robson S, Stirrups K, Valsesia A, Walter K, Wei J, Tyler-Smith C, Carter NP, Lee C, Scherer SW, Hurles ME. Origins and functional impact of copy number variation in the human genome. Nature. 2010;464:704–12.
Patterson N, Price AL, Reich D. Population Structure and Eigenanalysis. PLoS Genet. 2006;2:e190.
Cardin N, Holmes C, The Wellcome Trust Case Control Consortium, Donnelly P, Marchini J. Bayesian hierarchical mixture modeling to assign copy number from a targeted CNV array. Genet Epidemiol. 2011;35:536–48.
Kutalik Z, Johnson T, Bochud M, Mooser V, Vollenweider P, Waeber G, Waterworth D, Beckmann JS, Bergmann S. Methods for testing association between uncertain genotypes and quantitative traits. Biogeosciences. 2011;12:1–17.
Manichaikul A, Chen W-M, Williams K, Wong Q, Sale M, Pankow J, Tsai M, Rotter J, Rich S, Mychaleckyj J. Analysis of family- and population-based samples in cohort genome-wide association studies. Hum Genet. 2012;131:275–87.
The GTEx Consortium. The Genotype-Tissue Expression (GTEx) pilot analysis: Multitissue gene regulation in humans. Science. 2015;348:648–60.
Westra H-J, Peters MJ, Esko T, Yaghootkar H, Schurmann C, Kettunen J, Christiansen MW, Fairfax BP, Schramm K, Powell JE, Zhernakova A, Zhernakova DV, Veldink JH, Van den Berg LH, Karjalainen J, Withoff S, Uitterlinden AG, Hofman A, Rivadeneira F, ’t Hoen PAC, Reinmaa E, Fischer K, Nelis M, Milani L, Melzer D, Ferrucci L, Singleton AB, Hernandez DG, Nalls MA, Homuth G, et al. Systematic identification of trans eQTLs as putative drivers of known disease associations. Nat Genet. 2013;45:1238–43.
Lonsdale J, Thomas J, Salvatore M, Phillips R, Lo E, Shad S, Hasz R, Walters G, Garcia F, Young N, Foster B, Moser M, Karasik E, Gillard B, Ramsey K, Sullivan S, Bridge J, Magazine H, Syron J, Fleming J, Siminoff L, Traino H, Mosavel M, Barker L, Jewell S, Rohrer D, Maxim D, Filkins D, Harbach P, Cortadillo E, et al. The Genotype-Tissue Expression (GTEx) project. Nat Genet. 2013;45:580–5.
Nakka KK, Chaudhary N, Joshi S, Bhat J, Singh K, Chatterjee S, Malhotra R, De A, Santra MK, Dilworth FJ, Chattopadhyay S. Nuclear matrix-associated protein SMAR1 regulates alternative splicing via HDAC6-mediated deacetylation of Sam68. Proc Natl Acad Sci. 2015;112:E3374–83.
Chakraborty S, Das K, Saha S, Mazumdar M, Manna A, Chakraborty S, Mukherjee S, Khan P, Adhikary A, Mohanty S, Chattopadhyay S, Biswas SC, Sa G, Das T. Nuclear Matrix Protein SMAR1 Represses c-Fos-mediated HPV18 E6 Transcription through Alteration of Chromatin Histone Deacetylation. J Biol Chem. 2014;289:29074–85.
Lam HC, Cloonan SM, Bhashyam AR, Haspel JA, Singh A, Sathirapongsasuti JF, Cervo M, Yao H, Chung AL, Mizumura K, An CH, Shan B, Franks JM, Haley KJ, Owen CA, Tesfaigzi Y, Washko GR, Quackenbush J, Silverman EK, Rahman I, Kim HP, Mahmood A, Biswal SS, Ryter SW, Choi AMK. Histone deacetylase 6-mediated selective autophagy regulates COPD-associated cilia dysfunction. J Clin Invest. 2013;123:5212–30.
Ito K, Ito M, Elliott WM, Cosio B, Caramori G, Kon OM, Barczyk A, Hayashi S, Adcock IM, Hogg JC, Barnes PJ. Decreased Histone Deacetylase Activity in Chronic Obstructive Pulmonary Disease. N Engl J Med. 2005;352:1967–76.
Yang J, Gao J, Adamian M, Wen X-H, Pawlyk B, Zhang L, Sanderson MJ, Zuo J, Makino CL, Li T. The Ciliary Rootlet Maintains Long-Term Stability of Sensory Cilia. Mol Cell Biol. 2005;25:4129–37.
Wang K, Li M, Hakonarson H. ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data. Nucleic Acids Res. 2010;38:e164–4.
This research used the ALICE and SPECTRE High Performance Computing Facilities at the University of Leicester. We acknowledge the Wellcome Trust Case Control Consortium for making data available about SNP tagging of common CNVs [http://www.wtccc.org.uk/wtcccplus_cnv/supplemental.shtml]. We acknowledge the SpiroMeta and CHARGE consortia for look up of SNP associations for replication. We acknowledge the UK BiLEVE study for look up of SNP associations for replication. This research has been conducted using the UK Biobank Resource.
Generation Scotland authors are Jennifer Huffman and Caroline Hayward at the Institute of Genetics and Molecular Medicine, University of Edinburgh Western General Hospital, Crewe Road, Edinburgh EH4 2XU, UK (lead author contact: email@example.com). UK BiLEVE lead author contact is Ian P Hall, Medical School, Queen’s Medical Centre, Nottingham, NG7 2UH, UK (firstname.lastname@example.org). ALSPAC: We are extremely grateful to all the families who took part in this study, the midwives for their help in recruiting them, and the whole ALSPAC team, which includes interviewers, computer and laboratory technicians, clerical workers, research scientists, volunteers, managers, receptionists and nurses. This publication is the work of the authors and Nick Shrine and Louise Wain will serve as guarantors for the contents of this paper.
This work was supported by Medical Research Council Senior Clinical Fellowship [grant number G0902313 to Martin Tobin]. The research was part-funded by the National Institute for Health Research (NIHR). The views expressed are those of the authors and not necessarily those of the National Health Service, the National Institute for Health Research or the Department of Health. SHIP is part of the Community Medicine Research network of the University of Greifswald, Germany, which is funded by the Federal Ministry of Education and Research (grants no. 01ZZ9603, 01ZZ0103, and 01ZZ0403), the Ministry of Cultural Affairs as well as the Social Ministry of the Federal State of Mecklenburg-West Pomerania, and the network ‘Greifswald Approach to Individualized Medicine (GANI_MED)’ funded by the Federal Ministry of Education and Research (grant 03IS2061A). Genome-wide data have been supported by the Federal Ministry of Education and Research (grant no. 03ZIK012) and a joint grant from Siemens Healthcare, Erlangen, Germany and the Federal State of Mecklenburg- West Pomerania. The University of Greifswald is a member of the ‘Center of Knowledge Interchange’ program of the Siemens AG. UK BiLEVE was funded by a Medical Research Council (MRC) strategic award (MC_PC_12010).
Availability of data and materials
The data sets supporting the results of this article are included within the article (and its additional files).
LVW designed the study. NRGS, MDT, LVW wrote the manuscript. NRGS, LVW, CS, MSA performed the analysis. CS, JH, QWA provided data formatting and summaries. TL, OTR, CEP, DPS, GH, SG, SBF, DME, JH, RG, LJP, GE, JH, CH, AM, BM, ALJ provided data. CS, JH, RG, DPS, OTR provided additional text. All authors read and approved the final manuscript.
The author(s) declare that they have no competing interests.
Consent to publication
Ethics approval and consent to participate
Ethical approval was obtained from all 6 cohorts.
The Busselton Health Study genetics study is approved by the University of Western Australia Human Ethics Committee under project numbers RA/4/1/1516 and RA/4/1/2077. Access to Busselton data was approved by the Research Committee for The Busselton Population Medical Research Foundation (approval number SN10/06).
The Young Finns Study has been approved by the Ethics Committee of the South-western Finland Hospital District. Access to Young Finns data was approved by the Young Finns Study group.
The British 1958 birth cohort biomedical follow-up (2002–2004), which included the DNA collection on which all subsequent genetic association studies have been based, was approved by the South East England Multi-Centre Research Ethics Committee (reference: MREC/01/1/44). Access to British 1958 Birth Cohort data was approved by the British 1958 Birth Cohort Access Committee/Access Committee for CLS Cohorts (approval: 2009_DATA_05_Wain).
The Study of Health in Pomerania was approved by the local ethics committee of the University of Greifswald. Access to Study of Health in Pomerania data were via the Community Medicine Research Network, Department for Management and Transfer of Data and Biomaterials of the University of Greifswald (http://www.medizin.uni-greifswald.de/icm/transferstelle/).
Recruitment to the Raine Study and all follow-ups were approved by the Human Ethics Committee at King Edward Memorial Hospital and/or Princess Margaret Hospital for Children (PMH). Access to the Raine data was approved by the Raine Study Executive Committee.
Ethical approval for the Avon Longitudinal Study of Parents and Children (ALSPAC) was obtained from the ALSPAC Ethics and Law Committee and the Local Research Ethics Committees. All data provided for the analyses was anonymised and no patient identifying information was held by the central analysis group. Access to the Avon Longitudinal Study of Parents and Children was approved by the ASLPAC Executive Committee (approved project B1186, http://www.bristol.ac.uk/alspac/researchers/data-access/).
About this article
Cite this article
Shrine, N., Tobin, M.D., Schurmann, C. et al. Genome-wide association study of copy number variation with lung function identifies a novel signal of association near BANP for forced vital capacity. BMC Genet 17, 116 (2016). https://doi.org/10.1186/s12863-016-0423-0
- Copy number variation
- Lung function
- Genome-wide association study