- Open Access
Contribution of genetic variation to transgenerational inheritance of DNA methylation
- Allan F McRae1, 2Email author,
- Joseph E Powell1, 2,
- Anjali K Henders3,
- Lisa Bowdler3,
- Gibran Hemani1, 2,
- Sonia Shah1, 2,
- Jodie N Painter3,
- Nicholas G Martin3,
- Peter M Visscher†1, 2 and
- Grant W Montgomery†3
© McRae et al.; licensee BioMed Central Ltd. 2014
- Received: 4 November 2013
- Accepted: 29 May 2014
- Published: 29 May 2014
Despite the important role DNA methylation plays in transcriptional regulation, the transgenerational inheritance of DNA methylation is not well understood. The genetic heritability of DNA methylation has been estimated using twin pairs, although concern has been expressed whether the underlying assumption of equal common environmental effects are applicable due to intrauterine differences between monozygotic and dizygotic twins. We estimate the heritability of DNA methylation on peripheral blood leukocytes using Illumina HumanMethylation450 array using a family based sample of 614 people from 117 families, allowing comparison both within and across generations.
The correlations from the various available relative pairs indicate that on average the similarity in DNA methylation between relatives is predominantly due to genetic effects with any common environmental or zygotic effects being limited. The average heritability of DNA methylation measured at probes with no known SNPs is estimated as 0.187. The ten most heritable methylation probes were investigated with a genome-wide association study, all showing highly statistically significant cis mQTLs. Further investigation of one of these cis mQTL, found in the MHC region of chromosome 6, showed the most significantly associated SNP was also associated with over 200 other DNA methylation probes in this region and the gene expression level of 9 genes.
The majority of transgenerational similarity in DNA methylation is attributable to genetic effects, and approximately 20% of individual differences in DNA methylation in the population are caused by DNA sequence variation that is not located within CpG sites.
- Twin Pair
- Epigenetic Inheritance
- Genetic Heritability
- Transgenerational Inheritance
- Common Environmental Effect
DNA methylation is a crucial epigenetic mark associated with regulation of regulating cellular processes including the silencing of gene expression, differentiation and maintaining genomic stability . A growing number of human diseases have been found to be associated with defects in DNA methylation [2, 3]. Importantly, DNA methylation (along with other epigenetic changes) provides a biological link between an individual’s environmental exposures and their phenotype.
Despite the important role DNA methylation plays in transcriptional regulation, the transgenerational inheritance of DNA methylation is not well understood. Two forms of inheritance of epigenetic state have been demonstrated: genetic inheritance and epigenetic inheritance. With genetic inheritance, an individual’s underlying DNA sequence affects epigenetic state, with the extreme example being a genetic variant at a CpG locus that can disrupt DNA methylation at this site. Less understood is the role that DNA sequence variation outside of the CpG locus plays in the observed variation in DNA methylation. Epigenetic inheritance is the sequence independent transmission of epigenetic marks across generations and can occur through the incomplete erasure of epigenetic marks during the two major epigenetic reprogramming events that happen at the gamete and zygote stages. Examples of epigenetic inheritance in the mouse include the agouti viable yellow (A vy ) and axin-fused (Axin Fu ) alleles [4, 5]. Demonstration of epigenetic inheritance in humans remains unsubstantiated, but is supported through circumstantial evidence such as epidemiological studies noting the effect of grandparental food supply on body size and mortality in their grandchildren [6–8]. The relative importance of genetic inheritance, epigenetic inheritance and common environmental influences to locus specific DNA methylation similarity among relatives has not been well estimated on a genome-wide scale.
A number of studies based on limited numbers of twin pairs have shown significantly higher genome-wide average correlations in DNA methylation measures in monozygotic (MZ) twins compared to dizygotic (DZ) twins, indicating a significant genetic component underlying variation in DNA methylation . Studies using the Illumina HumanMethylation27 array found average estimates of heritability of 0.18 and 0.19 in whole blood  and 0.12, 0.07 and 0.05 in cord blood mononuclear cells, umbilical vascular endothelial cells and placenta, respectively . Both these studies used fewer than 20 of each MZ and DZ pairs in the estimation of heritability. The differences between average correlations in DNA methylation for MZ and DZ pairs broadly confirmed that observed in previous studies conducted with fewer CpG sites [12, 13]. The case for genetic heritability of DNA methylation is also confirmed by genome-wide association studies locating a number methylation quantitative trait loci (mQTL) in both cis and trans locations [10, 14–17].
The interpretation of differences in correlations between MZ and DZ twin pairs is subject to assumptions  that are potentially violated when dealing with epigenetic data. In particular, the higher correlation between MZ twin pairs could be partially due to a common epigenentic starting point in MZ twins at the zygotic stage . It is also unclear whether the assumption of equal common environmental influence on the trait in both MZ and DZ twins is applicable to the analysis of DNA methylation due to the different intrauterine environment experienced by the types of twins, in terms of both chorionicity and implantation, and the role of intrauterine environment on shaping the neonatal epigenome .
In this study, we investigate the role of genetic heritability in the similarity of DNA methylation between generations using a family based sample of 614 individuals from 117 families consisting of twin pairs, their parents and siblings using DNA methylation measures on peripheral blood lymphocytes typed on Illumina HumanMethylation450 arrays. This allows us to assess the extent of transgenerational inheritance of DNA methylation caused by genetic heritability.
The majority of the similarity in DNA methylation levels between relatives is due to genetic effects
Average correlation across all probes of normalised methylation measurements between relative pairs
It is likely that a proportion of probes on the array show no variation in DNA methylation in peripheral blood lymphocytes. While there was no clear cutoff observed in the between those probes with only experimental noise in their DNA methylation level estimates and those with low levels of genuine DNA methylation variation, we can examine the effect of non-variable positions by comparing probes with high levels of observed variation to those with low levels (Additional file 3: Figure S3). The probes with the lowest observed variation show a reduction in their average estimated heritability. However, excluding the 25% of probes with the lowest observed variation only increases the average estimated heritability to 0.212 from 0.199, demonstrating any bias introduced by including probes in regions with invariant DNA methylation is limited.
We estimated the effect of environment on the similarity of DNA methylation by fitting a common environment effect for the nuclear families in addition to the additive genetic effect. Given the nuclear family design used in this study, the effects of common environment and epigenetic inheritance are highly confounded and so difficult to estimate separately. Thus the estimated common environmental effect will be inflated by potential epigenetic inheritance. The estimated common environmental variance was small, with an average of 2.3%. Overall, 56% of sites had an estimated zero common environmental variance. While this is greater than the 50% expected under the null hypothesis, attributable to the bias created when trying to separate out the correlated additive genetic and common environment effects in this sample size, it does provide a strong indication that the common environment of a nuclear family explains very little variation in DNA methylation levels. Similarly, none of the probes show a significant common environmental variance at a Benjamini-Hochberg false discovery rate of 5%.
Effect of cellular composition on heritability estimates
It has been shown that at some loci the DNA methylation level when measured from peripheral blood leukocytes is reflective of the underlying cell composition. To exclude this as a driving force behind the heritability estimates, we estimated the proportion of monocytes, B cells, natural killer, CD4+ and CD8+ T-cells and granuloctyes from the DNA methylation data . We then included the estimated proportion of each of these cell types as covariates while estimating the heritability of each DNA methylation probe. Correcting for the cellular make-up reduced the average heritability estimate of DNA methylation by 0.199 to 0.176. As shown in Additional file 4: Figure S4, the cellular composition of the samples had little effect on the heritability estimates for the majority of probes investigated. In particular, the heritability estimates for probes showing high heritability were relatively stable. Probes with lower heritability showed more bias due to cellular composition, although this was limited to a subset of approximately 7% of the probes.
Excluding SNPs effects on genetic heritability estimates of DNA methylation
Using the 1000 Genomes Phase I Version 3 data from European individuals , the number of SNPs and their location in each probe was investigated. Additional file 5: Figure S5 shows that the average methylation heritability substantially increases with the number of SNPs within a probe region. This increase in DNA methylation genetic heritability can be attributed to genuine DNA methylation differences caused by SNPs at the CpG site or through cis genetic effects, or alternatively to a SNP causing differences in binding of alternative alleles to the array. This effect is further investigated in Additional file 6: Figure S6 where the average genetic heritability is correlated with the position on the SNP in the probe for all probes containing a single known SNP. It is evident that the primary increase in genetic heritability is when the SNP is within the CpG site, although this effect does extend across the whole probe with the average genetic heritability being greater than that observed in probes that do not overlap known SNPs. To avoid potential biases in estimates of genetic heritability due to effects of SNPs on array binding, we removed all probes with known SNPs from the dataset. The average genetic heritability of the remaining 303,078 probes was 0.187, slightly less than the estimate of 0.199 obtained including all probes. Of this subset, 141,596 (46.7%) were significantly genetically heritable at Benjamini-Hochberg false discovery rate of 5%.
The effect of genomic context on genetic heritability of DNA methylation
Differences in average heritability for different ‘HIL’ categories of the measured CpGs  separated by the two probe types on the Illumina HumanMethylation450 array
Average heritability estimate
Type I probes
Type II probes
Identification of complex genetic associations with DNA methylation and gene-expression
Details of the 10 most heritable probes that do not contain any annotated SNPs
4.8 × 10-78
3.0 × 10-105
8.1 × 10-84
8.8 × 10-58
2.9 × 10-101
1.4 × 10-107
1.8 × 10-77
Upstream (MIR4520B)/Downstream (MIR4520A)
1.3 × 10-91
2.1 × 10-105
2.9 × 10-101
Additional file 9: Figures S8a-i provide equivalent plots for the 8 Mbp region surrounding the most significant GWAS SNP for the remaining nine of the 10 most heritable probes. Association signals for these SNPs extended only a few hundred kbp into the surrounding region with one exception. SNP rs10021525 was associated with methylation measured by a single probe. Of the other SNPs, rs10848167 was significantly associated with 109 probes at a genome-wide Bonferroni corrected level. The majority of SNPs showed associations with effects on methylation in both increasing and decreasing directions. None of these nine SNPs were significantly associated with gene-expression after correction for genome-wide multiple testing.
We have demonstrated significant genetic control for the transgenerational inheritance of DNA methylation. Of particular importance, genetic heritability is shown to be the major cause of similarity in DNA methylation levels among relatives when considering the average across the genome. This study conclusively demonstrates that previous small scale studies on twin pairs [10, 11] are not greatly biased in their genetic heritability estimates through potential zygotic effects due to MZ twins starting from a common epigenetic state . However, estimates for twin pairs were observed to be slightly more similar to each other than to their siblings, indicating that small environmental or zygotic effect exists, although the contribution to similarity among relatives is at least an order of magnitude less than the estimated genetic heritability. Similarly, while direct testing failed to detect any significant common environmental influence on DNA methylation on the scale of the nuclear family, there was a small non-zero average parent-parent correlation observed indicating that such effects may be found in larger studies. This small correlation between parents may suggest some aspect of assortative mating, although these families show no evidence for assortative mating based on DNA sequence variant information . It is also plausible that the parent-parent correlation could be explained by unaccounted for experimental artefacts, as while the plating position and batch for each individual was completely randomised on the DNA methylation arrays, family groups tended to have blood collected at the same time.
Investigating epigenetic inheritance in an outbred population is difficult. When fitting a mixed linear model to nuclear families such as those used in this study, it is particularly difficult to separate out common environmental effects from potential epigenetic inheritance. As these effects are confounded, the observation of no significant common environmental effects observed in our data suggests that epigenetic inheritance is not widespread at these loci. However, this is not a directly test for epigenetic inheritance and a number of different models (involving no correlation between the spouses and potentially inheritance occurring through only the maternal or paternal lines) could be formed to test this. Using this approach to detect epigenetic inheritance would require a very large sample size in order to separate the various competing models for the action of both epigenetic inheritance and common environmental effects.
A potential bias to estimating genetic heritability of DNA methylation in arrays is the role of SNPs in the probe locations. While some SNPs cause genuine DNA methylation differences - such as those found in the CpG site - they may also affect the binding of the probe to the array. The effect of SNPs within probe sequences was minimised by using data from the European cohort of the 1000 Genomes Project  and excluding all probes with known variants (approximately 27%). Given the evidence for cis genetic effects on DNA methlylation, this is probably too stringent a filter in that it removes genuine heritable genetic variation in DNA methylation. It is likely that not all genetic sequence variation in the probe regions has yet been detected in the 1000 Genomes Project. However, given the effect of SNPs within the probes on average heritability was shown to be limited and any non-detected variant will be at low frequency in the population, such variants will have only a small effect on the heritability estimates presented.
A GWAS of the 10 most genetically heritable DNA methylation probes in our data found large cis mQTL. Notably, the most heritable DNA methylation probe is located in the MHC region, which is known to be associated with a wide range of diseases and other complex traits  providing potential insight to the biological mechanisms underlying these associations. The top SNP at this mQTL was associated with more than 200 DNA methylation probes in the surrounding 8 Mbp region and also with expression at 10 genes. The length of the associated region was unique among the cis mQTL the top 10 most heritable probes, but a more extensive GWAS analysis for all probes across the genome is required to assess the length distribution of genomic regions influenced by mQTLs and whether the MHC region is unique. Also of interest was the bidirectional effect of associations with both increased and decreased DNA methylation and expression levels. Such effects were replicated in many of the other top 10 most heritable DNA methylation probes indicating the complex pattern was not solely due to the known complex linkage disequilibrium structure in the MHC region. It has been demonstrated that DNA methylation can affect gene-expression in either a passive or active manner . Our results show associations both increasing and decreasing DNA methylation and gene-expression and it is difficult to infer a simple biological mechanism behind these associations from this dataset.
In summary, we have provided convincing evidence that the majority of transgenerational similarity in DNA methylation is attributable to genetic effects, and that approximately 20% of individual differences in DNA methylation in the population are caused by DNA sequence variation that is not located within CpG sites.
DNA methylation was measured on 614 individuals from 117 families of European descent recruited as part of a study on adolescent twins and selected from individuals in the Brisbane Systems Genetics Study . Families consist of adolescent MZ and DZ twins, their siblings and their parents. This study was approved by the Human Research Ethics Committee of the Queensland Institute for Medical Research. All participants gave informed written consent. DNA was extracted from peripheral blood lymphocytes by the salt precipitation method  from samples that were time matched to sample collection of PAXgene tubes for gene expression studies in the Brisbane Systems Genetics Study .
Bisulfite conversions were performed in 96 well plates using the EZ-96 DNA Methylation Kit (Zymo Research, Irvine, CA, USA). Prior to conversion, DNA concentrations were determined by NanoDrop quantification (NanoDrop Techologies, Inc., Wilmington, DE, USA) and standardised to include 500 ng. Three technical replicates were included in each conversion to assess repeatability. A commercial female human genomic DNA sample (Promega Corporation, Madison, WI, USA) was used on all plates, one sample from each run was duplicated on the plate and one sample duplicated from a different plate. DNA recovery after conversion was quantified using Nanodrop (Thermo Scientific, Wilmington, DE, USA).
Bisulfite converted DNA samples were hybridised to the 12 sample, Illumina HumanMethylation450 BeadChips using the Infinium HD Methylation protocol and Tecan robotics (Illumina, San Diego, CA, USA). The HM 450 BeadChip-assessed methylation status was interrogated at 485,577 CpG sites across the genome. It provides coverage of 99% of RefSeq genes. Methylation scores for each CpG site are obtained as a ratio of the intensities of fluorescent signals and are represented as β-values. Samples were randomly placed with respect to the chip they were measured on and to the position on that chip in order to avoid any confounding with family. DNA methylation data are available at the Gene Expression Omnibus under accession code GSE56105.
Box-plots of the red and green intensity levels and their ratio were used to ensure that no chip position was under- or over-exposed, with any outlying samples repeated. Similarly, the proportion of probes with detection P value less than 0.01 was examined to confirm strong binding of the sample to the array. Probes on the sex chomosomes or having been annotated as binding to multiple chromosomes  were removed from the analysis, as were those with zero CpG sites. The probability of a probe within a sample either being called as missing or with a detection P value less than 0.001 were estimated from the average rate across all probes and samples. A threshold for probes showing significant deviation from random missingness (or excess poor binding) was determined by testing against a binomial distribution for the number of samples at the 0.05 significance level with a Bonferroni correction for the number of probes. Any probe with more than 11 individuals with missing data or more than five individuals with detection P values > 0.001 were removed. After cleaning, 417,069 probes remained. A flow chart depicting the data cleaning and the number of arrays and probes removed at each stage is given in Additional file 10: Figure S1.
No global normalisation was performed on the methylation arrays as, for example, quantile normalisation may remove genetic and environmental effects that act globally on methylation. Individual probes were normalised across all samples using a generalised linear model with a logistic link function. Corrections were made for the effects of chip (which encompasses batch processing effects), position on the chip, sex, age, age2, sex × age and sex × age2. All heritability analyses were performed using the residuals from this model. No correction for differences between the two probe types was performed as the heritability analysis is partitioning the variation within a particular probe, so the observed shrinking of the Type II probes away from measures of 0 and 1 does not have an effect on the results.
To avoid undue influence of outlying data points (which could either be genuine unique methylation differences or measurement error) on both the estimates of heritability and following GWAS analysis, any measurement greater than five interquartile ranges from its nearest quartile was set to missing. The choice of threshold was determined by comparing heritability estimates with and without outliers included and noting the point at which outliers affected the results (data not shown).
Where MS B is the Mean Square Between pairs and MS W is the Mean Square Within.
As the relationship pairs indicated that on average common environment effects are small, the heritability for each probe was estimated by partitioning its variance into additive genetic (V a ) and environmental (V e ) components. Additionally, a model which included a nuclear family common environmental effect (V f ) was tested. All models were fitted using QTDT v2.6.1 .
Genome-wide association analysis
Genome-wide association analyses were performed on the 10 most heritable probes without known SNPs within the probe. All individuals were genotyped on Illumina 610-Quad Beadchip arrays. Full details of genotyping procedures are given elsewhere . Standard QC filters were applied, leaving 528,509 SNPs. The remaining genotyped SNPs were phased using HAPI-UR  and imputed using 1000 Genomes Phase I Version 3  with Impute V2 [31, 32]. Raw imputed SNPs were filtered to remove any SNPs with low imputation quality as defined by an R2 < 0.8. Subsequent quality control removed SNPs with MAF <0.05, those with HWE p < 1 × 10-6, and a missing rate >10%. After filtering, 6,005,138 SNPs remained for further analysis. Association analysis on the imputed genotype probabilities was performed using Merlin .
Gene expression was measured on peripheral blood lymphocytes using the Illumina HT-12 v4.0 array and the data were normalised as described in detail elsewhere . The individuals used in this study represent a subset of the cohort with gene-expression measurements. After cleaning, 17,926 probes remained for association testing. Gene expression data are available at the Gene Expression Omnibus under accession code GSE53195.
We gratefully acknowledge the participation of the twins and their families. We thank Marlene Grace, Ann Eldridge and Kerrie McAloney for sample collection and processing; the staff of the Molecular Epidemiology Laboratory at QIMR for DNA sample processing and preparation; Harry Beeby, David Smyth for IT support; and Dale Nyholt and Scott Gordon for their substantial efforts involving the QC and preparation of the GWA datasets. This research was supported by NHMRC grants 1010374, 496667 and 1046880, and the National Institutes of Health (NIH) grants GM057091 and GM099568. GWM and PMV are supported by the NHMRC Fellowship Scheme, and JEP is supported by an Australian Research Council DECRA. We acknowledge funding by the Australian Research Council (A7960034, A79906588, A79801419, DP0212016, DP0343921), and the Australian National Health and Medical Research Council (NHMRC) Medical Bioinformatics Genomics Proteomics Program (grant 389891) for building and maintaining the adolescent twin family resource through which samples were collected. The funders had no role in study design, data collection and analysis, decision to publish or preparation of the manuscript.
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