DNA methylation and transcriptional noise
© Huh et al.; licensee BioMed Central Ltd. 2013
Received: 1 June 2012
Accepted: 5 April 2013
Published: 26 April 2013
The Erratum to this article has been published in Epigenetics & Chromatin 2014 7:13
DNA methylation is one of the most phylogenetically widespread epigenetic modifications of genomic DNA. In particular, DNA methylation of transcription units (‘gene bodies’) is highly conserved across diverse taxa. However, the functional role of gene body methylation is not yet fully understood. A long-standing hypothesis posits that gene body methylation reduces transcriptional noise associated with spurious transcription of genes. Despite the plausibility of this hypothesis, an explicit test of this hypothesis has not been performed until now.
Using nucleotide-resolution data on genomic DNA methylation and abundant microarray data, here we investigate the relationship between DNA methylation and transcriptional noise. Transcriptional noise measured from microarrays scales down with expression abundance, confirming findings from single-cell studies. We show that gene body methylation is significantly negatively associated with transcriptional noise when examined in the context of other biological factors.
This finding supports the hypothesis that gene body methylation suppresses transcriptional noise. Heavy methylation of vertebrate genomes may have evolved as a global regulatory mechanism to control for transcriptional noise. In contrast, promoter methylation exhibits positive correlations with the level of transcriptional noise. We hypothesize that methylated promoters tend to undergo more frequent transcriptional bursts than those that avoid DNA methylation.
KeywordsDNA methylation Gene expression Spurious transcription Transcriptional noise
DNA methylation at CpG dinucleotides is a key epigenetic modification in the human genome crucial for regulatory and developmental processes [1, 2]. The degree of DNA methylation in the human genome is extensive: most CpG dinucleotides are methylated in most tissues and developmental stages examined [3–6]. In particular, transcription units, or so-called ‘gene bodies’, are even more heavily methylated than the surrounding intergenic regions [6–9].
The functional consequences of promoter methylation on chromatin configuration and transcriptional regulation are extensively documented (see, for example, [10–12]). There is also considerable evidence suggesting that DNA methylation suppresses proliferation of transposable elements (TEs) [13–15]. However, the role of gene body methylation remains largely unresolved. Recently, studies have begun to identify molecular consequences of gene body methylation. For example, gene body methylation affects pol II occupancy and histone modifications . Differential levels of DNA methylation between different exons have been linked to differential inclusion and exclusion of specific exons in transcripts [17, 18]. Gene body methylation may also occur as a byproduct of transcriptional processes . Another possibility is that gene body methylation is simply an extension of methylation of TEs; many genes harbor TEs within their transcription units, and the main role of methylation is to suppress the proliferation of these TEs .
Nevertheless, the main role of gene body DNA methylation remains unresolved. In fact, it is considered as one of the most long-standing open questions regarding genomic DNA methylation [20–25]. This question is even more pertinent in light of evolutionary patterns of DNA methylation. Comparative DNA methylation studies indicate that gene body methylation is the most conserved, ancestral form of genomic DNA methylation [7, 9, 23, 26]. Thus, elucidating the role of gene body DNA methylation may provide significant insights into the evolutionary divergence of genomic DNA methylation across taxa [9, 23, 26, 27].
A long-standing hypothesis posits that gene body DNA methylation suppresses spurious transcription within coding regions. By doing so, gene body methylation can effectively reduce ‘transcriptional noise’ [27, 28]. This hypothesis is based upon the well-accepted idea that DNA methylation is generally repressive . Pervasive DNA methylation of gene bodies, and the consequent suppression of transcriptional noise, may have served as a key facilitator enabling the evolution of complex vertebrate genomes . Moreover, recent studies have begun to indicate that epigenetic mechanisms are deeply implicated in regulation of gene expression variability [30–33].
However, a detailed analysis of the relationship between transcriptional noise and DNA methylation has been lacking until now, due in large part to technical difficulties. Here, capitalizing on the recent progress in genomics and epigenomics, we investigated the impact of DNA methylation on transcriptional noise, using data from the human genome. Our analyses provide, for the first time, unequivocal evidence supporting the role of gene body methylation to reducing transcriptional noise. Furthermore, we show that promoter DNA methylation is also highly significantly associated with transcriptional noise.
Transcriptional noise is negatively correlated with expression abundance and associate with specific functions
Levels of gene expression vary between cells even with the same genetic materials and under the same biological conditions [34–36]. Understanding the nature and mechanism of such variability, which is commonly referred to as ‘transcriptional noise’, has manifold functional consequences . Recently, there have been significant improvements in experimental methods to measure transcriptional noise, as well as in the theoretical understanding of transcriptional noise. These studies indicate that transcriptional noise may occur due to transcriptional bursting of promoters, as well as spurious transcription within coding sequences [38–41].
Transcriptional noise in multicellular organisms, such as mammals, cannot be easily dissected using experimental means. However, they can be approximated using abundant expression datasets, for example utilizing normalized variation among microarray assays between replicates of populations [42, 43]. For example, Yin et al.  compared the transcriptional noise measured from microarrays to those measured from single-cell experiments. The two results correspond remarkably well . Similar results were seen in another study, comparing expression variation among populations to experimentally measured transcriptional noise . Following these approaches, in this study we approximated transcriptional noise of human genes as the coefficient of variation of transcriptional abundance, assayed between replicates of populations of the same tissue samples under normal conditions (see Methods).
There have been significant recent technical improvements in analysis of genomic DNA methylation. In particular, researchers have begun to generate whole-genome maps of DNA methylation at the nucleotide level, via whole-genome sequencing of bisulfite-converted genomic DNA [5, 44, 45]. This method quantifies the methylation level of each CpG dinucleotide across the whole genome, enabling us to discern gene body methylation levels for individual genes.
In this study, we analyzed DNA methylation and transcriptional noise of the prefrontal cortex (brain) and the peripheral blood mononuclear cells (blood). We chose these two tissues for the following reasons. First, we decided to analyze ‘normal’ tissues (as opposed to cell lines). While there exists vast information on transcriptional variation of cell lines, gene expression profiles of cell lines are known to have significantly diverged from those of normal tissues . Consequently, we chose not to consider cell lines in the current study. Second, we chose tissues whose genome-wide methylation maps are currently available. Finally, large numbers of microarray data in the ‘control’ (as opposed to disease) conditions exist for these tissues, thereby enabling us to measure transcriptional noise with confidence. We used rigorous quality control processes to curate microarray data from these tissues (see Methods). The resulting data are from the same technical platforms, and exhibit high correlation levels among experiments (Additional files 1 and 2).
Gene body methylation and promoter methylation exhibit negative and positive associations with transcriptional noise
Our interest was in determining whether DNA methylation influences transcriptional noise. To do so, we needed to first account for the effect of expression abundance on both of these variables. This is because DNA methylation is intimately related to expression abundance [6, 10, 23, 25], and gene expression abundance is correlated with transcriptional noise (Figure 1). In addition, other genomic variables, such as gene lengths, are also correlated with expression abundance [49, 50].
Our goal was to explain the variation found in the levels of transcriptional noise using several explanatory (independent) variables. We used the following variables as explanatory variables: expression abundance, gene body methylation, promoter methylation, and gene lengths. We first examined the variance inflation factors (VIFs), which are indicators of multicolinearity among variables. None of the explanatory variables exhibited VIFs greater than 5. This demonstrated that we could assess individual contributions of each genomic trait without the influence of multicolinearity .
Multiple linear regression models explaining variation of transcriptional noise in different tissues
Estimate of β
Gene body methylationa
Log (gene length)a
Gene body methylationa
Log (gene length)1
Multiple linear regression models explaining variation of transcriptional noise in different tissues
Estimate of β
Gene body methylation1
Log (gene length)a
Gene body methylation1
Log (gene length)a
Robust regression analyses (quantile regression for median) for the model used in Table 1
Estimate of β
Gene body methylationa
Log (gene length)a
Gene body methylationa
Log (gene length)a
Accounting for technical noise and among individual variability of DNA methylation
One potential caveat of our approach is the presence of technical noise, or variation of gene expression caused by technical variation among experiments, on the level of gene expression variability. Our interest is in the biological variability of gene expression. As defined previously, we approximated ‘transcriptional noise’ as the coefficient of variation (CV) among the replicates of expression data, as used previously . However, this measure of gene expression variability is a composite of biological noise, which is our main interest, plus technical variation among experiments. This is problematic because it is possible that technical noise might be confounded with biological noise. For example, technical variation among experiments is negatively correlated with the expression level of genes [56, 57]. Thus, it is important to take into account the impact of technical noise in assessing the relationship between biological noise and DNA methylation.
Multiple linear regression models in which technical versus biological components of transcriptional noise are separately analyzed
Estimate of β
Gene body methylation
Gene body methylation
Regression analysis accounting for individual variation indicates little effect of between-individual variability of DNA methylation on transcriptional noise
Sum of square
Degrees of freedom (df)
Gene body methylation
Individual:gene body methylation
The human genome and other vertebrate genomes are heavily methylated in most tissues and developmental stages, a pattern referred to as ‘global’ DNA methylation . This pattern is very different from what is observed in other animals and plants. In most invertebrates examined, DNA methylation is targeted to the transcription units (gene bodies) of a subset of genes [7, 9, 23]. Notably, gene body methylation appears to have existed well before the emergence of DNA methylation of promoters and TEs, as an ancestral form of DNA methylation in diverse animal and plant genomes [23, 60, 61].
Determining the role of gene body methylation is of much interest, and studies are revealing associations between gene body methylation and gene expression [9, 21, 62, 63], transcript composition [17, 18, 64] and chromatin structures . Nonetheless, the global role of gene body methylation remains unresolved. In this respect, two long-standing hypotheses stand out. The first hypothesis posits that gene body methylation reduces transcriptional noise . Another hypothesis focuses on the impact of DNA methylation to suppress the proliferation of TEs . Many TEs are found in gene bodies, thus methylation of TEs may have caused expansive methylation of gene bodies .
In this study we examined the predictions of these two hypotheses using whole genome methylation data and statistical methods. Because gene body methylation and transcriptional noise are both significantly correlated with expression abundance, it is important to analyze the impact of gene body methylation while considering the effect of expression abundance. We used several statistical methods to achieve this goal. We also examined the impact of noise due to technical variation among experiments, as well as between-individual variation of DNA methylation on our results. These analyses all indicate that gene body methylation, when viewed in the context of other biological factors, has a negative relationship with transcriptional noise.
Transcriptional noise is abundantly present in diverse taxa. The origin of transcriptional noise may be related to ‘transcriptional bursts’, referring to the phenomenon that transcription tends to occur in bursts [65–67]. Transcriptional noise also occurs due to transcription of non-canonical promoters within gene bodies, potentially due to the overabundance of RNA polymerase II in cellular environment . Our results showing that more heavily methylated gene bodies exhibit less transcriptional noise are consistent with the idea that transcriptional noise is reduced by pervasive gene body methylation. Alternatively, the negative relationship between gene body DNA methylation and transcriptional noise may reflect an indirect association due to a third, yet unknown biological factor(s) that influence both variables.
The details of the actual underlying molecular mechanisms of such process are yet to be fully characterized. There are some well established epigenetic modifications of gene bodies are shown to directly suppress the initiation of non-canonical transcripts within coding sequences [68–70]. Emerging evidence indicate that gene body DNA methylation is likely to complement or function together with other epigenetic modifications to generate chromatin states that are repressive of the initiation and elongation of spurious transcripts. For example, DNA methylation of gene bodies reduces the efficiency of transcriptional elongation, by excluding RNA polymerase II occupancy and recruiting several repressive histone marks . Gene body DNA methylation effectively excludes deposition of the histone variant H2A.Z, which tend to mark lowly expressed genes with high expression variability among tissues and biological conditions . The identities of molecular components of the crosstalk between DNA methylation and histone modifications continue to be discovered (see, for example, ).
Interestingly, our analyses indicate that promoter DNA methylation is positively correlated with the level of transcriptional noise. The underlying molecular mechanism of this phenomenon is of great interest. One possibility is that this is related to the intrinsic susceptibility of specific promoters toward transcriptional bursting. In the simplest case, promoters appear to switch randomly between ‘ON’ and ‘OFF’ states with respect to the initiation of transcription [37, 47]. Some promoters, however, remain perpetually in the ‘ON’ state (permissive to transcription) and do not exhibit bursting . Such promoters exhibit less transcriptional variability compared to those undergoing switches between different transcriptional states . In other words, the degree of transcriptional bursting likely varies between promoters according to their propensity toward different transcriptional states, leading to different levels of transcriptional noise among genes.
Given that there exists considerable evidence that unmethylated promoters can maintain a ‘permissive’ chromatin state [72, 74], we hypothesize the following: promoters with lower level of DNA methylation are more likely to adopt and maintain a permissive transcriptional state (similar to the ‘ON’ state referred to above) and exhibit little transcriptional bursting. However, promoters that are more susceptible to DNA methylation may be more likely to undergo stochastic fluctuations between different states, facilitating transcriptional bursts, and as a consequence exhibit increased transcriptional noise. The actual molecular mechanisms underlying these processes are again likely to involve highly orchestrated interactions between DNA methylation and other epigenetic mechanisms: in particular, studies in yeast have revealed the role of nucleosome positioning in regulation of gene expression variability [31, 33].
Reducing transcriptional noise is particularly important for genes that perform housekeeping functions and are therefore constantly expressed . Indeed, methylation maps of distantly related animal genomes reveal that gene body methylation usually targets genes that function in ‘housekeeping’ cellular processes [26, 28, 75]. Thus, we hypothesize that gene body methylation functions as a primary mechanism to suppress transcriptional noise of essential housekeeping genes in diverse organisms. Gene body DNA methylation is the main mode of DNA methylation in many invertebrate species. Reducing transcriptional noise may serve as the primary function of DNA methylation in such genomes. Furthermore, the human genome is characterized by heavy transcription of non-coding regions [76, 77]. Global methylation of the whole genome may have evolved as a molecular mechanism to reduce global transcriptional noise .
Moreover, we found that methylation of TEs within gene bodies also contributes to the suppression of transcriptional noise. Several studies now indicate that methylation of TEs may have evolved after the evolution of gene body methylation [23, 61]. It will be interesting to determine whether the origin of TE methylation is related to its function to reduce intragenic transcriptional noise. Our study cannot provide a clear resolution to this question. Analyses of genomic methylation patterns of species straddling the invertebrate-vertebrate boundaries (near the origin of global DNA methylation) will be informative to determine the evolutionary sequences of these processes.
We explored the relationship between transcriptional noise and DNA methylation, using gene expression variability among different populations of cells as a proxy for transcriptional noise. Our analysis confirms the inverse relationship between gene expression abundance and transcriptional noise, while revealing novel relationships between DNA methylation and transcriptional noise. In particular gene body DNA methylation exhibits a negative correlation with transcriptional noise. This observation supports a longstanding hypothesis that gene body DNA methylation may reduce transcriptional noise. In light of evolutionary findings that gene body methylation is a widespread, conserved form of DNA methylation, the ancestral role of DNA methylation may have been related to the reduction of transcriptional noise. On the other hand, promoter DNA methylation is positively related to transcriptional noise, raising the possibility that epigenetic status of promoters may affect transcriptional bursts.
Gene expression data was obtained from National Center for Biotechnology Information (NCBI) Gene Expression Omnibus (http://www.ncbi.nlm.nih.gov/geo/) (Additional file 7). Because there are considerable technical variations between platforms, we restricted platforms to only the Affymetrix Human Genome U133 series. After quality control, we obtained a total of 52 datasets (12 datasets for the prefrontal cortex and 40 datasets for blood). Gene lengths were determined based upon the RefSeq annotation provided by the UCSC genome browser. Nucleotide resolution whole DNA methylation maps of the human prefrontal cortex (brain) were obtained from a recent study (, data available at NCBI Gene Omnibus under the record number GSE37202). DNA methylation maps of mature peripheral blood mononuclear cells were from Li et al. , generated using a similar method.
To obtain gene body methylation levels of non-repetitive portions of genes, we used the annotation of TEs from the RepeatMasker database (http://www.repeatmasker.org). A custom Perl script was used to mask the TEs in gene bodies. For each mapped cytosine, the fractional methylation value was calculated as: total number of ‘C’ reads/(total number of ‘C’ reads + total number of ‘T’ reads), following previous studies [5, 8, 44]. We then calculated the fractional methylation level of each transcription unit, using the RefSeq database of hg18. Gene body methylation level for each gene was estimated as the mean fractional methylation value for all the mapped cytosines within each transcription unit. When alternative transcripts were present, we chose the longest transcript for each gene. The promoter methylation level for each gene was estimated as fractional methylation for regions spanning 1,500 bp upstream and 500 bp downstream of the transcription start site (TSS), similar to Zeng et al. .
Microarray data processing
Microarray raw data files were first processed using raw intensity using the MAS5.0 method . Using other normalization methods provided similar results. We used the median probe intensities assigned to each gene as gene expression levels. We then analyzed correlation between pairwise samples, to assess similarities between datasets from the same tissue. Datasets within the same tissues exhibiting correlation coefficient greater than 0.8 are included in this study (Additional files 1 and 2). Quantile normalization using the R package ‘preprocesscore’  was conducted within each tissue. Transcriptional noise was defined as the coefficient of variation (CV: standard deviation/mean) of transcriptional abundance within each tissue, following Yin et al. .
Multiple linear regression models of transcriptional noise
We performed multiple linear regression analyses to elucidate relationships between transcriptional noise and several biological factors (gene expression abundance, gene body methylation, promoter methylation, and gene lengths) simultaneously. CV and gene length were log transformed to improve normality. Our analyses indicated that the gender is not a significant variable and thus excluded from further analyses. We also examined the significance of the interaction terms between predictors. The results showed that the interaction terms were generally not significant and they were therefore removed from subsequent analyses.
Robust regression analysis was performed using various loss functions. We summarized the result of quantile regression in Table 3. We also used other well-known loss functions such as bisquare, Hampel and Huber (Additional file 6) [53–55]. All these approaches provided consistent results to those of the ordinary least squares method. Therefore, we conclude that the significance and magnitude of the explanatory variable effect is essential.
Functional enrichment analyses
Functional enrichment pattern of specific subsets of genes was assessed using the DAVID tools (http://david.abcc.ncifcrf.gov/) . We used the list of genes included in our analyses as the background, and tested enrichments of specific gene ontology terms using the GO FAT annotation. We examined the mean transcriptional noise of genes in the two tissues and investigated the specific gene ontology terms for top 5% high transcriptional noise genes and 5% low transcriptional noise genes. A Benjamini multiple testing correction of the EASE score (a modified Fisher exact P value) was used to determine statistical significance of gene enrichment.
This study was supported by a National Research Foundation of Korea (NRF) grant funded by the Korean government (2012R1A3A2026438) to TP and by Georgia Tech Fund for Innovation in Research and Education (GT-FIRE) and NSF grants (MCB-0950896 and BCS-0751481) to SVY. We thank Hema Nagrajan for computational support.
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