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Age-related accrual of methylomic variability is linked to fundamental ageing mechanisms

  • Roderick C. Slieker1,
  • Maarten van Iterson1,
  • René Luijk1,
  • Marian Beekman1,
  • Daria V. Zhernakova2,
  • Matthijs H. Moed1,
  • Hailiang Mei3,
  • Michiel van Galen4,
  • Patrick Deelen2,
  • Marc Jan Bonder2,
  • Alexandra Zhernakova2,
  • André G. Uitterlinden5,
  • Ettje F. Tigchelaar2,
  • Coen D. A. Stehouwer6,
  • Casper G. Schalkwijk6,
  • Carla J. H. van der Kallen6,
  • Albert Hofman7,
  • Diana van Heemst8,
  • Eco J. de Geus9,
  • Jenny van Dongen9,
  • Joris Deelen1,
  • Leonard H. van den Berg10,
  • Joyce van Meurs5,
  • Rick Jansen11,
  • Peter A. C. ‘t Hoen4,
  • Lude Franke2,
  • Cisca Wijmenga2,
  • Jan H. Veldink10,
  • Morris A. Swertz12,
  • Marleen M. J. van Greevenbroek6,
  • Cornelia M. van Duijn13,
  • Dorret I. Boomsma9,
  • BIOS consortium,
  • P. Eline Slagboom1 and
  • Bastiaan T. Heijmans1Email author
Genome Biology201617:191

Received: 26 April 2016

Accepted: 1 September 2016

Published: 22 September 2016



Epigenetic change is a hallmark of ageing but its link to ageing mechanisms in humans remains poorly understood. While DNA methylation at many CpG sites closely tracks chronological age, DNA methylation changes relevant to biological age are expected to gradually dissociate from chronological age, mirroring the increased heterogeneity in health status at older ages.


Here, we report on the large-scale identification of 6366 age-related variably methylated positions (aVMPs) identified in 3295 whole blood DNA methylation profiles, 2044 of which have a matching RNA-seq gene expression profile. aVMPs are enriched at polycomb repressed regions and, accordingly, methylation at those positions is associated with the expression of genes encoding components of polycomb repressive complex 2 (PRC2) in trans. Further analysis revealed trans-associations for 1816 aVMPs with an additional 854 genes. These trans-associated aVMPs are characterized by either an age-related gain of methylation at CpG islands marked by PRC2 or a loss of methylation at enhancers. This distinct pattern extends to other tissues and multiple cancer types. Finally, genes associated with aVMPs in trans whose expression is variably upregulated with age (733 genes) play a key role in DNA repair and apoptosis, whereas downregulated aVMP-associated genes (121 genes) are mapped to defined pathways in cellular metabolism.


Our results link age-related changes in DNA methylation to fundamental mechanisms that are thought to drive human ageing.


DNA methylationAgeing450kDNA damageVariability


Studies of model organisms such as yeast, nematodes, and mice have shown that the accumulation of cellular damage is a fundamental cause of ageing across species [13]. Epigenetic dysregulation is thought to play a key role in this process [4, 5]. Numerous human population studies have now shown that changes in DNA methylation of CpG dinucleotides, a key epigenetic mechanism [6], are strongly associated with chronological age. Although these epigenetic changes are in part a by-product of age-related changes in the cellular composition of the studied tissue [79], many age-related differentially methylated positions (aDMPs) observed in blood samples are independent of cell composition [819]. Additional studies showed the consistent occurrence of aDMPs in other tissues [2022] and species [23] and aDMPs have proven to be a useful tool to predict chronological age [24, 25].

However, aDMPs may not be the most informative marker of the ageing process since they were discovered as close correlates of chronological age instead of biological age [26]. Moreover, only a small proportion of aDMPs are associated with expression changes [12, 17], suggesting that their functional implication may be limited. In contrast, DNA methylation changes that increasingly diverge from chronological age may reflect the increasing inter-individual variation in health that occurs with increasing age. Initial studies, although small or lacking a genome-wide view, indicated that an increasing variability of DNA methylation with age indeed exists [21, 27, 28]. A recent large twin study showed that genetic factors explain a minor proportion of the variation in DNA methylation in the population, while the influence of environmental and stochastic factors is large and commonly increases with age [19].

In the current study, we charted the occurrence of age-related variably methylated positions (aVMPs) across the genome. We evaluated the methylation at 429,296 CpG sites for increased variability with age in whole blood samples from 3295 individuals. After validation using multiple external datasets and integration of methylome with transcriptome data (n = 2044), we show that aVMPs link to the expression of genes in trans that play a central role in fundamental ageing mechanisms.


To uncover the occurrence of divergence in DNA methylation with age, we studied 3295 whole-blood DNA methylation profiles encompassing 429,296 CpGs of individuals aged 18 to 88 years (Fig. 1a; Additional file 1a, b). To obtain global evidence for an increasing DNA methylomic divergence between individuals with age, we calculated the Shannon entropy on the individual level [25, 29]. With age, we observed a distinct increase in the variability in the Shannon entropy (adjusted for age, sex, and blood cell composition), suggesting that the level of order between individuals becomes more variable at older ages (Fig. 1b).
Fig. 1

Discovery of aVMPs in whole blood of 3295 individuals. a Flow chart of the different sets of CpGs identified in the current study, in cis and in trans. QC quality control. b Shannon entropy (y-axis) against age (x-axis) in 3295 individuals. c Volcano plot of the DNA methylation change in average (x-axis) against the change in variability (y-axis). d Examples of the three classes of aVMPs identified: aVMPs without a change in average (constant-aVMPs, cg21752383), aVMPs with a gain in DNA methylation (gain-aVMPs; cg01873886), and aVMPs with a loss in methylation (loss-aVMPs; cg14127336)

To map the specific CpGs that change in variability with age (age-related variably methylated positions or aVMPs), we tested for an increase in variability with age, independent of an average change in DNA methylation with age (aDMP effects) and changes in blood cell composition. We identified 8265 aVMPs that showed a robust increase in variability with age (P < 10−7 and ≥5 % increase per 10 years; Fig. 1a, c). The number of aVMPs was substantially smaller than aDMPs in our data set: approximately a quarter of the CpGs tested were identified as aDMPs (99,466 CpGs, no effect size cutoff; Fig. 1a; Additional file 1d); the majority of the CpGs did not show an age-related change in DNA methylation (321,565 CpGs; Fig. 1a; Additional file 1c). The number of aVMPs showing a decrease in variability with age was exceedingly small (19 aVMPs, P < 10−7 and ≥5 % decrease per 10 years) and these aVMPs were excluded from further analyses (Fig. 1c). Since increases in variability at hypo- or hypermethylated CpGs can only go in one direction (up for DNA methylation levels near 0 and down for those near 1), we observed that 48.2 % of the aVMPs were also identified in these data as aDMPs (3980 aVMPs; Fig. 1c). Of note, only 213 aVMPs (2.6 %) overlapped with previously reported aDMPs (n = 7477) [7, 8, 14, 16, 18, 25] and six aVMPs overlapped with CpGs from the Horvath clock (n = 353) [24] (Additional file 1e). Hence, aVMPs represent a new and distinct class of age-related changes in DNA methylation. Clustering analysis showed that aVMPs could be categorized into three groups: aVMPs hypomethylated in young individuals that gained DNA methylation with age (both average and variability; gain-aVMPs), hypermethylated aVMPs that lost DNA methylation with age (both average and variability; loss-aVMPs) and intermediate-methylated aVMPs where gains and losses with age were balanced, resulting in the absence of an aDMP effect (constant-aVMPs) (Fig. 1d).

We validated the aVMPs in two large public datasets consisting of whole blood (n = 643, age range 20–102, median 65 years) [25] and purified monocytes, a relative homogeneous population of blood cells (n = 1202, age range 44–83, median 59 years) [17]. This validation step was incorporated to exclude that our results were confounded by the fact that we analyzed multiple population studies of different ages or by age-related changes in the cellular composition of blood. The increase in variability observed in the discovery data was remarkably concordant with the effect size in both validation datasets (Fig. 2a). In total, 6366 aVMPs (78.4 %) were validated in both datasets (Fig. 2b; Additional file 2).
Fig. 2

Validation of aVMPs in whole blood of 643 and purified monocytes of 1202 individuals. a Change in variability in the discovery (x-axis) against the whole blood and monocyte validation (y-axis) datasets. Red dots represent the monocyte validation dataset, blue dots represent the whole blood validation dataset. b The aVMPs that validate in whole blood and monocytes. c Density plot of average DNA methylation of validated aVMPs in the discovery dataset and validation datasets

Although we corrected for cell heterogeneity using the major blood cell subtypes, age-related changes in the percentage of less frequent cell subtypes could also have introduced aVMPs. To further exclude that the increased variability was driven by changes in blood cell composition, we repeated our aVMP analysis with the inclusion of predicted, more refined blood cell subtype fractions (CD8+ T cells, CD4+ T cells, natural killer (NK) cells, B cells, and granulocytes) [30]. Out of the 6366, 6343 (99.6 %) were again identified as aVMPs (P FDR  ≤ 0.05). Furthermore, we compared the DNA methylation of whole blood to that of blood cell subtypes and their progenitors using five public data sets on 19 cell types (Additional file 3). The methylation of aVMPs was highly concordant between whole blood and the various cell subtypes, indicating aVMPs cannot be attributed to the outgrowth of a specific cell subtype, but instead represent genuine age-related changes in DNA methylation. Conversely, CpGs differentially methylated between blood cell subtypes [31] had the same, if not smaller, chance of being an aVMP (odds ratio = 0.56; P = 0.19).

The validated set of 6366 robust and consistent aVMPs was taken forward for in-depth analysis. aVMPs were characterized by an intermediate methylation level (Fig. 2c). Among the 6366 aVMPs, a similar number of gain-aVMPs and loss-aVMPs were found (2788 gain-aVMPs, 3578 loss-aVMPs). While some individuals showed differential DNA methylation on many of the identified aVMPs (marked by vertical bands in Additional file 1f), others did not show any difference in DNA methylation. The individual-specific changes in DNA methylation with age also resulted in an age-related loss of correlation between individuals on the 6366 aVMPs (Additional file 1g).

aVMPs are depleted in active regions and enriched in PcG repressed regions

To characterize the genomic regions harboring aVMPs, we obtained the chromatin state segments of blood cell types (Epigenomics Roadmap [32]), which reflect the biological function of the underlying region in blood cells on the basis of combinations of histone modifications [32]. A pronounced enrichment was found for aVMPs in the segments marking a repressed genome, including repressed polycomb (7.2-fold enrichment, P < 0.0001), weak repressed polycomb (2.3-fold enrichment, P < 0.0001) and heterochromatin (2.5-fold enrichment, P < 0.0001), while aVMPs were depleted for active segments, including strong transcription (0.04-fold enrichment, P < 0.0001) (Fig. 3a; Additional file 4b). In absolute terms, 4212 aVMPs (66.2 %) mapped to segments marking repressed DNA. These data were supported by a parallel enrichment of aVMPs for repressive histone modifications (Additional file 4a) and for binding sites of the PcG repressive complex 2 (PRC2) protein EZH2 in the ENCODE blood cell line GM12878 (2.1-fold enrichment, P < 0.0001).
Fig. 3

Characterization of genomic regions harboring aVMPs and associations of gene expression in cis. a Enrichment (odds ratio, y-axis) of aVMPs in chromatin state segments (x-axis) in blood. b Overlap between chromatin state segmentation data in blood and in human embryonic stem cells (hESCs). Numbers represent the number of aVMPs that overlap between segments. c Frequency of aVMPs (y-axis) in 100-kb windows across the genome (blue bars) and their association with gene expression in cis in red. d Frequency of age-related variably methylated regions (aVMRs; x-axis) on each of the autosomal chromosomes (y-axis). e Increased variability (y-axis, top panel) of the protocadherin cluster (bottom panel). Abbreviations: TssA Active transcription start site, TssAFlnk flanking active transcription start site, TxFlnk transcription at gene 5′ and 3′, Tx strong transcription, TxWk weak transcription, EnhG genic enhancers, Enh enhancers, ZNF/Rpts ZNF genes plus repeats, Het heterochromatin, TssBiv bivalent/poised transcription start site, BivFlnk flanking bivalent transcription start site/enhancer, EnhBiv bivalent enhancer, ReprPC repressed polycomb, ReprPCWk weak repressed polycomb, Quies quiescent/low

To explore whether the methylation level of aVMPs was associated with gene expression in cis (i.e., gene and aVMP within 500 kb), we studied the relationship between DNA methylation and gene expression using 2044 individuals for whom both DNA methylation and gene expression data (RNA-seq) were available. Despite predominantly mapping to repressed regions, 1988 cis-aVMPs out of the 6366 aVMPs (31.2 %; Fig. 1a; Additional file 5) were associated with gene expression of 1549 genes in cis (see Additional file 4c for HOXC4 and PCDHB6 examples). Gene Ontology (GO) analysis of the cis-associated genes showed enrichment for processes involved in neuron differentiation and neuron development (P < 0.0001).

Since age-related divergence was found to be overrepresented near developmental genes, we also mapped aVMPs to chromatin state segments of a human embryonic stem cell line (H1-hESC). Interestingly, repressed genomic regions in blood harboring an aVMP were often a (bivalent) transcription start site or (bivalent) enhancer in the H1-hESC line (Fig. 3b), highlighting the developmental history of regions accumulating aVMPs.

In line with the enrichment for developmental genes, we found a large number of aVMPs near (neuro)developmental genes (Fig. 3c). To investigate whether aVMPs clustered into regions, we identified age-related variably methylated regions (aVMRs) [33]. This resulted in 160 aVMRs encompassing 527 aVMPs (8.3 %; Additional file 6). aVMRs were particularly frequent on chromosomes 5 and 19 (Fig. 3d), the former of which could be attributed, in part, to eight aVMRs (totalling 26 aVMPs) that mapped to the protocadherin gene cluster (Fig. 3e).

aVMPs are associated with expression of genes in trans

The enrichment of aVMPs in polycomb-repressed regions and PRC2 binding sites suggests a role for PcG proteins in the occurrence of aVMPs. Indeed, methylation at the majority of aVMPs was positively associated with the expression of components of the PRC2, including EED, SUZ12, and EZH2, particularly when an aVMP mapped to an EZH2 binding site (Additional file 7a). Further analysis revealed that trans-associations were not limited to PRC2 components. Of the total number of 6366 aVMPs, 1816 (28.5 %) were associated with expression of 854 coding genes in trans (4.6 % of genes tested; Fig. 4a; Additional file 8), i.e., the aVMP and gene on different chromosomes or on the same chromosome but 5 Mb apart. The association between aVMP methylation and gene expression implies an increase in variance in gene expression in conjunction with DNA methylation. Of note, the number of associations between trans-genes and trans-aVMPs was high. For example, the expression of TPRG1 was associated with 1296 correlated aVMPs and, conversely, the aVMP cg13246235 located near PHACTR1 was associated with 853 associated trans-genes (Fig. 4b).
Fig. 4

Identification and characterization of aVMPs associated with gene expression in trans. a Correlation between DNA methylation of 1816 aVMPs (columns) and gene expression of 854 genes (rows). b TPRG1 is associated with 1296 aVMPs and cg13246235 with the expression of 853 genes. Blue lines represent the associations between the gene expression of TPRG1 and the DNA methylation of 1296 aVMPs. Red lines represent the associations between the DNA methylation of cg13246235 and the expression of 853 genes. c Z-score of individuals (columns) versus young individuals (<30 years) of trans-aVMPs (rows). The bar on the bottom left represents the average DNA methylation (DNAm) at a young age (<30 years). The bar on the top represents the age from low age (white) to high age (green). d Fraction and enrichment of gain- and loss-aVMPs in genomic features. CGI CpG island. Blue, fraction of loss-aVMPs; purple, fraction of gain-aVMPs. e Enrichment (odds ratio, y-axis) of gain- and loss-aVMPs in chromatin state segments (x-axis). f Average DNA methylation of aVMPs in various cancer types compared with their normal tissue counterpart. Abbreviations: TssA Active transcription start site, TssAFlnk flanking active transcription start site, TxFlnk transcription at gene 5' and 3', Tx strong transcription, TxWk weak transcription, EnhG genic enhancers, Enh enhancers, ZNF/Rpts ZNF genes plus repeats, Het heterochromatin, TssBiv bivalent/poised transcription start site, BivFlnk flanking bivalent transcription start site/enhancer, EnhBiv bivalent enhancer, ReprPC repressed polycomb, ReprPCWk weak repressed polycomb, Quies quiescent/low

Trans-aVMPs encompassed two classes (instead of three in the complete set of aVMPs): 994 gain-aVMPs that, apart from increasing in variability with age, gained methylation and were hypomethylated in young individuals; and 822 loss-aVMPs that lost DNA methylation with age and were hypermethylated in young individuals (Figs. 1a and 4c). The genomic context of gain- and loss-aVMPs was markedly different. Gain-aVMPs were strongly enriched for CpG islands (CGIs) compared with loss-aVMPs (22.9-fold, P < 0.0001), while being depleted for non-CGI regions (Fig. 4d; 0.05-fold, P < 0.0001). Conversely, loss-aVMPs were highly enriched for non-CGI regions (19.0-fold, P < 0.0001; Fig. 4d). These results are in line with the fact that CGIs are commonly hypomethylated and hence can only gain DNA methylation, while non-CGI regions tend to be hypermethylated and preferentially lose DNA methylation. Furthermore, loss-aVMPs were generally found in active regions (transcription flanking, 4.3-fold enrichment, P < 0.01), but also in weak polycomb repressed regions (3.7-fold enrichment, P < 0.0001) (Fig. 4e). Gain-aVMPs were overrepresented in repressed and bivalent regions and particularly in PcG repressed regions (11.5-fold enriched, P < 0.0001; Fig. 4e). The enrichment analysis yielded similar results when gain- and loss-aVMPs were evaluated separately: both types were enriched for polycomb repressed regions and gain-aVMPs were enriched for bivalent domains. Bivalent domains have been associated with an enrichment for linear age-related DNA methylation changes [8].

Next, we investigated whether the age-related gain and loss of methylation at the trans-aVMPs extended beyond blood using publically available datasets. Gain-aVMPs showed a similar or even larger change in average methylation with age in, for example, colon (91.2 % concordant direction, P < 0.0001), lung (89.6 %, P < 0.0001), skin (87.0–93.3 %, P < 0.0001) and SAT (89.0 %, P < 0.0001) (Additional file 9). For loss-aDMPs, evidence for age-related changes in the same direction was found in lung (75.0 %, P < 0.0001), colon (70.9 %, P < 0.0001), and skin (56.3–66.1 %, P < 0.01). Within skin [34], age-related DNA methylation changes were most pronounced in the epidermis (compared with dermis), with the strongest effect sizes in sun-exposed epidermis samples. In view of the assumed commonalities between ageing and cancer, we investigated whether the changes also extend to different tumors given that gain of DNA methylation at CGIs is a hallmark of tumor biology [35]. Gain-aVMPs were found to show relative hypermethylation and loss-aVMPs hypomethylation, respectively, across various cancer types, including blood, bladder, colon, and lung cancer (P < 0.0001; Fig. 4f), which suggests a striking similarity between age-affected and cancer methylomes, in line with previous observations for aDMPs [36]. Taken together, aVMPs are largely driven by tissue-independent factors, but these changes may be accelerated by external influences (like sun exposure) and tumorigenesis.

aVMP-associated trans-genes linked to DNA damage and apoptosis

The expression of genes associated with aVMPs in trans unambiguously clustered into two highly correlated gene sets (Fig. 5a). An age-affected methylome was associated with down-regulated expression of trans-genes in a cluster of 121 genes and with up-regulated expression of a larger cluster of 733 genes. GO analysis showed that down-regulated genes are involved in various intra-cellular metabolic pathways, including pentose metabolism and regulation of CDC42 GTPase activity (Fig. 5b), of which the former remained significant when using a permutation-based enrichment test (Additional file 10). Key genes in the pentose metabolism process whose expression was associated with aVMP methylation included PYGL, TALDO1, and PGD (Fig. 5b, c). Up-regulated trans-genes were intimately involved in apoptosis, cell cycle, DNA repair, and lymphocyte activation (Fig. 5b) and these enrichments were also observed using the permutation-based enrichment test (20,000 permutations; Additional file 10). The process unifying these pathways might be the cell damage response encompassing the upregulation of DNA repair, cell cycle changes, and upregulated apoptosis. In each category, key genes were identified, including the ERCC genes (DNA repair), CDKN2A (encoding the INK4A/ARF locus), BUB3 (checkpoint), and CASP7 (apoptosis) (Fig. 5c). Of note, a small proportion of the identified genes were previously found to be correlated with chronological age in 14,983 samples (163 genes, 19.1 %; Additional file 7b) [37], illustrating that the trans-genes we identified here represent, to a large extent, a different phenomenon. In summary, aVMP DNA methylation is associated with the downregulation of expression of genes in intra-cellular metabolism pathways and the upregulation of expression of genes in ageing pathways.
Fig. 5

Annotation of genes associated with aVMP methylation in trans. a Correlation between genes associated with aVMP methylation in trans. b Enrichment of trans-genes in GO terms. c Examples of genes identified in each GO category


In a large-scale analysis we discovered and validated 6366 age-related variably methylated positions (aVMPs). These aVMPs were found to occur in three classes: gain-aVMPs that increase in variance and average DNA methylation with age, loss-aVMPs that increase in variance but decrease in average, and constant-aVMPs that increase in variance but with a constant average. aVMPs accrue in repressed regions that are characterized by both the PcG-deposited histone mark H3K27me3 and the binding site of EZH2, a component of PRC2. While aVMPs were commonly associated with the expression of (neuro)developmental genes in cis, they were linked to transcriptional activity of genes in trans that have a key role in well-established ageing pathways such as intracellular metabolism, apoptosis, and DNA damage response. Of interest, tumors were found to accumulate DNA methylation changes at CpG sites of aVMPs, thus supporting the long-standing notion that ageing and cancer are in part driven by common mechanisms [2].

Our data show that the genomic regions accumulating variability in ageing populations are highly specific and reproducible. Hence, although the increase in variability may have a stochastic component, the regions affected by this phenomenon are well-defined and not stochastic. aVMPs were discovered in whole blood samples (corrected for blood cell composition) and validated in independent whole blood and purified blood cell type (i.e., monocytes) samples. The results are thus unlikely to be driven by age-related changes in blood cell composition. Furthermore, we compared the DNA methylation of aVMPs to the DNA methylation of 19 blood cell subtypes and showed that the DNA methylation is highly concordant and, conversely, CpGs known to be differentially methylated between blood cell subtypes were not overrepresented among aVMPs. To our knowledge, our analyses together represent the most comprehensive validation of whole blood-discovered differential DNA methylation to date. Further support for the involvement of a cell type-independent phenomenon is the observation that aVMP methylation was associated with in cis and in trans expression of genes that function in developmental and ageing-related cellular processes, respectively, instead of immune pathways. To definitively confirm the cross-tissue occurrence of aVMPs, genome-wide DNA methylation data sets for internal tissues are required that have a similarly large size as those currently available for blood samples. Finally, aVMPs associated with gene expression in trans discovered in blood displayed a similar pattern of gain and loss of methylation with age across a series of tissues.

Importantly, our data indicate that aVMPs constitute a class of CpGs displaying age-related changes in the level of DNA methylation that is distinct from aDMPs. Known aDMPs rarely were aVMPs (2.6 % of 7477 previously reported aDMPs [7, 8, 14, 16, 18, 25]) and, in contrast to aDMPs, aVMPs showed striking associations with gene expression. Hence, aVMPs are not driven by changes in mean towards a methylation fraction of 0.5 that, in principle, could lead to an increased variance. This mathematical effect that cannot, however, be completely ruled out for all individual aVMPs.

aVMPs preferentially occur in repressed regions marked by PcG repression, namely the PcG binding site of EZH2 and repressive histone marks (H3K27me3). The integration of methylome with transcriptome data revealed that, in contrast to aDMP methylation, aVMP methylation is commonly associated with gene expression. Genes associated with aVMPs in cis frequently had a (neuro)developmental role exemplified by the HOX gene clusters, the protocadherin gene cluster, TBX genes, and ZIC genes. aVMPs reported here share the overrepresentation at PRC2-controlled regions with a subset of previously reported aDMPs [7, 8, 11, 12, 17, 36, 38], regions undergoing differential methylation observed in long-term cultured human senescent mesenchymal stem cells [39], various cancer types [7, 36], and, finally, regions displaying differential methylation in vitro after oxidative stress-induced DNA damage [40]. The latter study is of particular relevance to the interpretation of our results since it showed that oxidative DNA damage leads to PRC2 recruitment to sites with DNA damage [40] and results in translocation of DNA methyltransferases and EZH2 from CpG-poor regions to CG-rich regions, which in turn leads to hypermethylation of CGIs and hypomethylation at CpG-poor regions [40, 41]. We observed that aVMP methylation is frequently and strongly associated with the expression of PRC2 components in trans. Moreover, aVMPs were characterized by a gain of methylation at CGIs and a loss of methylation at CpG-poor regions. Our data highlight the potentially important role of altered PcG regulation in ageing.

Intriguingly, associations of aVMP methylation with gene expression in trans were not limited to PRC2 genes but extended to genes known to play a role in ageing. In older individuals who had an aged DNA methylation profile as compared with young individuals, we observed a downregulation of genes involved in metabolism. The upregulation of ageing pathways, as observed in old individuals with an aged methylome, has been reported previously in hematopoietic stem cells in mice and humans, for which macromolecular or DNA damage may be the driving force [42, 43]. Of note, many of the trans-genes we identified are involved in the DNA damage response and are frequently mutated in various cancers, including CDKN2A, DNMT3A, and TP53 [44]. Hence, genomic stress, due either to hyperproliferation or DNA damage, may drive upregulation of well-established ageing pathways, downregulation of intra-cellular metabolism, and altered regulation by PcG proteins associated with increased variability of DNA methylation.


In contrast to aDMPs, aVMPs show a striking variability in DNA methylation at higher ages. Two individuals of the same age may display highly distinct methylation patterns across aVMPs, where one of them may have a DNA methylation profile at aVMPs that is similar to that of young individuals. Therefore, aVMPs fulfill a primary prerequisite for a biomarker of biological age [26]. Further studies are required to establish whether aVMP-based methylation profiles mark health status and predict mortality. Finally, our study shows that large-scale integrative genomics studies are an effective approach toward the identification of fundamental processes involved in ageing and are complementary to experimental work in model organisms.



DNA methylation data and RNA-seq data were generated within the Biobank-based Integrative Omics Studies Consortium (BIOS Consortium; Additional file 11) [45, 46]. Discovery data generated within the BIOS consortium are available from the European Genome-phenome Archive (EGA) under accession number EGAC00001000277. The data comprise six Dutch biobanks: Cohort on Diabetes and Atherosclerosis Maastricht (CODAM) [47], LifeLines (LL) [48], Leiden Longevity Study (LLS) [49], Netherlands Twin Registry (NTR) [50], Rotterdam Study (RS) [51], and the Prospective ALS Study Netherlands (PAN) [52]. A random co-twin per twin pair from the Netherlands Twin Registry was included in the current dataset to restrict our analysis to unrelated individuals. Briefly, 500 ng of genomic DNA was bisulfite converted using the EZ DNA Methylation kit (Zymo Research, Irvine, CA, USA) and hybridized on Illumina Infinium 450 arrays according to the manufacturer’s protocols and signal intensities measured using an Illumina iScan BeadChip scanner. Sample identity of DNA methylation and expression data was confirmed with genotype data using MixupMapper [53]. Quality control (QC) on the DNA methylation data was performed using the R package MethylAid [54]. Out of the 3391 samples, 3296 samples passed QC. Data were normalized using functional normalization implemented in the R package minfi using five principal components [55]. Ambiguously mapped probes [56], probes with a high detection P value (>0.01), probes with a low bead count (<3 beads), and probes with a low success rate (missing in >95 % of the samples) were set to missing. Probes mapping to chromosomes X and Y were excluded from all analyses. Residual batch effects were removed using Combat as implemented in the R package SVA, with biobank as batch and gender and age as outcome variables [57].

RNA-seq comprised 2044 expression profiles for which also DNA methylation data were available. RNA libraries were prepared using the Illumina’s Truseq version 2 library preparation kit and paired-end sequenced of 2 × 50 bp using Illumina’s Hiseq2000. Using Illumina’s CASAVA, read sets per sample were generated and only reads passing the Chastity Filter were used for further processing. Using FastQC20 (v0.10.1) [58] initial QC was performed. Adapters were removed using cutadapt21 (v1.1) [59]. Using Sickle22 (v1.2) [60], low quality ends of the reads were trimmed (minimum length 25, minimum quality 20). Reads that passed QC were aligned to human genome build hg19 using STAR23 (v2.3.125) [61] and gene quantifications were based on Ensembl version 71. Gene counts were normalized for GC content and gene length using the R package cqn [62]. Associations between gene expression and DNA methylation were performed using voom-transformed values [63]. For graphical purposes normalized counts were transformed to RPKM values. Generation of methylome and transcriptome data was performed by the Human Genotyping facility (HugeF) of the ErasmusMC (the Netherlands,

Cell count data (neutrophils, lymphocytes, monocytes, eosinophils, and basophils) were available for the majority of the samples (>60 %). A prediction model for blood cell composition was fitted using a subset of the data for which cell counts were available using a multivariate partial-least-squares model (including age and gender) on the normalized DNA methylation data. Using the fitted model, the cell fractions were imputed for all samples and only these fractions were used in all analyses. Documentation and code are available in the R package wbccPredictor (available from Cell composition in the whole blood validation [25] dataset was also imputed using the described method. For the monocyte validation dataset, data on purity of the isolated cells was obtained from the Gene Expression Omnibus (GEO). To further confirm our results with the blood cell subtypes described by Houseman et al. [30], we used the implementation in the R package minfi [64] to impute the cell fractions of CD8+ T cells, CD4+ T cells, NK cells, B cells, and granulocytes.

Validation of aVMPs was performed in two external datasets, whole blood and monocyte datasets (Additional file 12). For the whole blood data, IDAT files used in Hannum et al. [25] were kindly provided by the authors. Data underwent the same quality and normalization procedure as used above. After quality control, 643 samples were used in subsequent samples. For the monocyte data, normalized data were obtained from the GEO [65] (accession number GSE56046 [17]). Raw DNA methylation data (Level 1; IDAT files) of healthy tissues and cancerous tissues were obtained from The Cancer Genome Atlas (TCGA Research Network,; Additional file 12) and underwent QC and normalization equal to the discovery data. Normalized DNA methylation data for subcutaneous fat were obtained from the ArrayExpress [66] (accession number E-MTAB-1866 [67]). Normalized dermis and epidermis DNA methylation data were downloaded from GEO under accession number GSE51954 [34]. Normalized data for cytogenetic normal acute myeloid leukemia (CN-AML) and healthy bone marrow CD34+ cells were downloaded from GEO under accession number GSE58477 [68].

Shannon entropy and aVMPs

All analyses were performed on the normalized whole dataset consisting of all biobanks together. To calculate the Shannon entropy, DNA methylation data were corrected for age, cell composition, and gender. Shannon entropy was calculated using a previously described method for DNA methylation data [25].

aVMPs were identified by using the Breusch–Pagan test for heteroscedasticity [69]. First, average change in age, blood cell composition, and gender were regressed out. Next, squared residuals were tested for an association with age with correction for blood cell composition and gender. aVMPs were defined as CpGs that showed a significant association between squared residuals and age with a Bonferroni corrected P value ≤0.05. Moreover, aVMPs were only selected if the increased variability with age was larger than 5 % per 10 years. aVMPs were further subdivided into three classes based on a clustering analysis: gain-aVMPs, loss-aVMPs, and constant-aVMPs. Gain-aVMPs were defined as CpGs that were hypomethylated at young age but where the change in average DNA methylation was positive (Fig. 1d middle panel). Loss-aVMPs were defined as CpGs that were hypermethylated at young age with a negative change in average DNA methylation with age (Fig. 1d bottom panel). Constant-aVMPs were defined as CpGs that were intermediately methylated and did not show a change in average but only in variance (Fig. 1d top panel).

For the association between DNA methylation of aVMPs and gene expression in cis, we only considered genes within 500 kb of the aVMP and we adjusted for gender and blood cell composition. The P value was corrected for multiple testing using the Bonferroni method for the number of genes tested in cis (P bonf ≤ 0.05). Next, the most significant associated gene (if any) was selected. Finally, the P value of each of these aVMP-gene pairs was corrected using the false discovery rate (FDR) method (P FDR ≤ 0.05) and only significant pairs were used [70].

In trans, we only evaluated aVMP and gene pairs that were >5 Mb away from each other on the same or on a different chromosome. P values for trans-associations were FDR corrected (P FDR ≤ 0.05 considered significant). Genes whose gene expression was associated with less than 5 % of all aVMPs (≤318 aVMPs, 6366) in trans were discarded.

Z-scores (compared to young) were calculated as a measure of directionality and magnitude of aberrant methylation of an aVMP within an individual:
$$ {Z}_{i,j}=\frac{\left({M}_{i,j}-\overline{M_{y,i}}\right)}{\sigma_{y,i}} $$
where Z i,j is the Z-score of the j th individual and i th aVMP, M i,j the DNA methylation of the j th individual and i th aVMP, \( \overline{M_{y,i}} \) the average DNA methylation in young individuals (<30 years) of the i th aVMP, and σ y,i the standard deviation in young individuals of the i th aVMP. All heatmaps were clustered based on Euclidian distance.

aVMPs were clustered to aVMRs using a method described before using default settings [33]. Genes were linked to aVMRs based on the nearest protein coding gene (Ensembl).

Annotations and integration with external data

Chromatin state segments were downloaded from the Epigenomics Roadmap for different blood cell subtypes [32]. CpGs were annotated to different segments based on the most frequent occurring feature in the various blood cell subtypes. Transcription factor binding sites (ChIP-seq) were obtained from the ENCODE project for all tissue types available [71]. CGI-centric annotations were obtained from previous work [33]. Enrichments were expressed as odds ratio on a log2 scale (if applicable).

GO enrichments were performed using the default settings of DAVID. To reduce redundancy in the GO enrichment terms, we used REVIGO with default settings [72]. Networks were plotted using Cytoscape version 3.2.1 [73]. The enrichment for gene sets was further verified with the gene set enrichment function (gseGO, biological processes) in the R package clusterProfiler [74] based on the fold change of the association between DNA methylation and gene expression in trans and 20,000 permutations.

To compare aVMPs in healthy tissues other than blood a linear model was fitted between DNA methylation and age for colon (TCGA), lung (TCGA), kidney (TCGA), bladder (TCGA), thyroid (TCGA), subcutaneous fat (GEO) [67] and skin (GEO) [34]. To compare healthy and cancerous tissues, data for the trans-aVMPs were obtained in CN-AML versus bone marrow CD34+ cells (GEO) [68], bladder urothelial carcinoma versus healthy bladder (TCGA), colon adenocarcinoma versus healthy colon (TCGA), kidney renal clear squamous cell carcinoma versus healthy kidney (TCGA), lung adenocarcinoma versus healthy lung (TCGA), and thyroid carcinoma versus healthy thyroid (TCGA).

Analyses were performed using R statistics, version 3.1.2. Figures were produced using ggplot2 [75], the Perl version of Circos (v0.67-7) [76] and Gviz [77].



Samples were contributed by LifeLines (, the Leiden Longevity Study (, the Netherlands Twin Registry (, the Rotterdam Study, (, the CODAM study ( and the PAN study ( All analyses were carried out on the Dutch national e-infrastructure with the support of SURF Cooperative. Members of the BIOS Consortium are listed in Additional file 11.


This work was done within the framework of the Biobank-Based Integrative Omics Studies (BIOS) Consortium funded by BBMRI-NL, a research infrastructure financed by the Dutch government (NWO 184.021.007 and within the European Union’s Seventh Framework Program IDEAL (FP7/2007-2011) under grant agreement number 259679.

Availability of data and materials

DNA methylation and gene expression data, generated within the BIOS Consortium, are available from the European Genome-phenome Archive (EGA) under accession number EGAC00001000277. The results shown here are in part based upon data generated by the TCGA Research Network:

Authors’ contributions

Conceptualization, RCS and BTH; methodology, RCS, BTH, MI, RL; investigation, RCS, BTH; writing (original draft), RCS, BTH; resources, MB, DVZ, MHM, HM, MvG, MJB, AZ, AGU, EFT, CDAS, CGS, CJHvdK, BAH, DvH, EJdeG, JvD, JD, LvdB, JvM, RJ, LF, CW, JHV, MMJvG, GMvD, DIB, ES. All authors read and approved the final manuscript.

Competing interests

The authors declare that they have no competing interests.

Ethics approval and consent to participate

Institutional review boards of the participating centers approved this study (CODAM, Medical Ethical Committee of the Maastricht University; LL, Ethics committee of the University Medical Centre Groningen; LLS, Ethical committee of the Leiden University Medical Center; PAN, Institutional review board of the University Medical Centre Utrecht; NTR, Central Ethics Committee on Research Involving Human Subjects of the VU University Medical Centre; RS, Institutional review board (Medical Ethics Committee) of the Erasmus Medical Center). Informed consent was given by all participants. Experimental procedures in this study comply with the Declaration of Helsinki.

Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (, which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver ( applies to the data made available in this article, unless otherwise stated.

Authors’ Affiliations

Molecular Epidemiology section, Leiden University Medical Center, Leiden, The Netherlands
Department of Genetics, University Medical Centre Groningen, Groningen, The Netherlands
Sequence Analysis Support Core, Leiden University Medical Center, Leiden, The Netherlands
Department of Human Genetics, Leiden University Medical Center, Leiden, The Netherlands
Department of Internal Medicine, Erasmus University Medical Center, Rotterdam, The Netherlands
Department of Internal Medicine and School for Cardiovascular Diseases (CARIM), Maastricht University Medical Center, Maastricht, The Netherlands
Department of Epidemiology, Erasmus University Medical Center, Rotterdam, The Netherlands
Department of Gerontology and Geriatrics, Leiden University Medical Center, Leiden, The Netherlands
Department of Biological Psychology, VU University Amsterdam, Neuroscience Campus Amsterdam, Amsterdam, The Netherlands
Department of Neurology, Brain Center Rudolf Magnus, University Medical Center Utrecht, Utrecht, The Netherlands
Department of Psychiatry, VU University Medical Center, Neuroscience Campus Amsterdam, Amsterdam, The Netherlands
Genomics Coordination Center, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands
Department of Genetic Epidemiology, Erasmus University Medical Center, Rotterdam, The Netherlands


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