Evaluating genome-wide DNA methylation changes in mice by Methylation Specific Digital Karyotyping
© Boon et al; licensee BioMed Central Ltd. 2008
Received: 07 May 2008
Accepted: 11 December 2008
Published: 11 December 2008
The study of genome-wide DNA methylation changes has become more accessible with the development of various array-based technologies though when studying species other than human the choice of applications are limited and not always within reach. In this study, we adapted and tested the applicability of Methylation Specific Digital Karyotyping (MSDK), a non-array based method, for the prospective analysis of epigenetic changes after perinatal nutritional modifications in a mouse model of allergic airway disease. MSDK is a sequenced based method that allows a comprehensive and unbiased methylation profiling. The method generates 21 base pairs long sequence tags derived from specific locations in the genome. The resulting tag frequencies determine in a quantitative manner the methylation level of the corresponding loci.
Genomic DNA from whole lung was isolated and subjected to MSDK analysis using the methylation-sensitive enzyme Not I as the mapping enzyme and Nla III as the fragmenting enzyme. In a pair wise comparison of the generated mouse MSDK libraries we identified 158 loci that are significantly differentially methylated (P-value = 0.05) after perinatal dietary changes in our mouse model. Quantitative methylation specific PCR and sequence analysis of bisulfate modified genomic DNA confirmed changes in methylation at specific loci. Differences in genomic MSDK tag counts for a selected set of genes, correlated well with changes in transcription levels as measured by real-time PCR. Furthermore serial analysis of gene expression profiling demonstrated a dramatic difference in expressed transcripts in mice exposed to perinatal nutritional changes.
The genome-wide methylation survey applied in this study allowed for an unbiased methylation profiling revealing subtle changes in DNA methylation in mice maternally exposed to dietary changes in methyl-donor content. The MSDK method is applicable for mouse models of complex human diseases in a mixed cell population and might be a valuable technology to determine whether environmental exposures can lead to epigenetic changes.
In eukaryotes DNA methylation occurs on cytosine residues of CpG dinucleotides. CpG islands, short genomic regions with a high frequency of CpG dinucleotides, are typically common near transcription start sites, and may be associated with promoter regions. These regions are not generally methylated in contrast to highly repetitive elements in the genome. DNA methylation can directly affect transcription by inhibiting binding of specific transcription factors and/or enhancing necessary chromatin remodeling for gene silencing. This process is required for normal embryonic development, imprinting, and X chromosome inactivation, and plays an important role in the normal functioning of an organism. Increasing numbers of studies are emphasizing the role of DNA methylation in human diseases [1–3]. Only until recently it has become clear that nutritional components can also affect epigenetic mechanisms like DNA methylation and can lead to long term phenotypic changes [4, 5].
The study of DNA Methylation has become more accessible by recent development of various technologies . The choice of methodology is highly dependent of the goal of the study, genome of interest and available resources. Most commercially available micro-array platforms are developed for restriction enzyme and affinity based assays like the short oligonucleotide arrays (Affymetrix), tiling arrays (NimbleGen) and CpG Island/promoter arrays (Agilent) . Like in other micro-array assays intensity changes are measured instead of actual levels of methylation and are subject for many sources of variation like array-lot variability and washing conditions. Whether the hybridization intensity will be proportional to the level of methylation is still uncertain and could be platform dependent. While these approaches are able to evaluate methylation changes throughout the entire genome, they remain expensive and are not generally accessible. Methylation Specific Digital Karyotyping (MSDK) is a non-micro array, genome-wide methylation analysis approach that relies on cleavage of genomic DNA with a methylation sensitive restriction enzyme. The concept of this approach is similar to serial analysis of gene expression (SAGE) and is based on the following principles: 21 bp sequence tags are derived from specific locations within the genome and can be directly matched to their corresponding loci, and concatenation of the sequence tags allows the serial analysis of multiple tags by high throughput sequencing [7, 8]. The resulting genomic tag frequencies determine in a quantitative manner the methylation level of the corresponding loci. In this report, we present a modification and application of MSDK, for the study of methylated loci throughout the mouse genome prenatally exposed to nutritional variations.
Results and discussion
Genome-wide DNA methylation analysis
In an effort to uncover candidate genes directly affected by DNA methylation in a mouse model of perinatal nutritional modification and allergic airway disease, we applied MSDK, a comprehensive, quantitative and unbiased genome-wide method that offers accurate information on the genomic position of differentially methylated loci. The MSDK method has been previously developed for the analysis of the human genome using the restriction enzyme Asc I as the mapping enzyme. The Asc I recognition site is preferentially found in CpG islands associated with transcribed genes . For our study of the mouse genome we considered the methylation sensitive enzymes Asc I, Sac II, Not I and Hpa II as the mapping enzyme in combination with Nla III as the fragmenting enzyme. There are over a million restriction sites for Hpa II in the mouse genome and 38,684 for Sac II. Although both enzymes are excellent cutters, we concluded that the sequencing costs would be too high. We found only 2,500 restriction sites for Asc I and 6,012 sites for Not I with a respective average fragment size of 280,000 bp and 130,000 bp. We selected Not I since the recognition site contains two CG dinucleotides and approximately 62% of these sites are associated with a CpG island in the mouse genome. Though not all the genes are associated with a CpG Island it has been estimated that at least 40% of the annotated genes have a CpG Island in their corresponding promoter region.
We sequenced 66,758 and 69,498 tags for respectively the HMD and the LMD MSDK libraries. After removal of all singletons, we found 8,323 experimental genomic tags of which 6,310 were present in both libraries, 967 were specific for the HMD and 1046 for the LMD library. In order to match the experimental tags to their corresponding genomic loci, virtual genomic tags were extracted from the mouse genome sequence as obtained from Ensembl http://www.ensembl.org using a python script http://www.python.org. This identified a total of 10,577 virtual tags of which 8,414 are unique. Alignment of the experimental tags with the 10,577 virtual tags showed that 5,533 (67%) could be matched to a unique position within the genome. A remaining 1,614 (19%) matched to multiple regions in the genome and 1,176 (14%) were not found. It is expected that the percentage of unmatched tags will decrease in time with the new releases of updated public mouse genome sequences. Comparison of the experimental tags with the virtual genomic tags per chromosome revealed an unbiased distribution of the experimental tags over the mouse genome (Figure 1b).
We identify differentially methylated loci in the mouse genome between the two libraries by applying the following selection criteria: mapping to a unique position to the mouse genome, and a fold difference in tag counts ≥ 5. Furthermore, in order to find genomic tags with a significant difference in tag counts we used a z-score to quantify the strength of the observed difference in the proportions of individual tag sequences in the two libraries and generate a P-value. We considered a P-value ≤ 0.05 as significant. Similar results were obtained when analyzing the data according to the sequence odds ratio and significance test http://cgap.nci.nih.gov/SAGE or the significance test available as part of the DiscoverySpace application . In this way, we identified 82 genomic tags with a higher count in the LMD library and 71 genomic tags with higher counts in the HMD [see Additional files 1 and 2] representing differentially methylated loci within the mouse genome (Figure 1c). The MSDK method screens for unmethylated restriction enzyme sites in the genome therefore higher genomic tag frequencies correspond with a decreased level of methylation. This implies that the 82 genomic tags with increased counts in the LMD library are likely to show an increased level of methylation in the HMD library. Despite the limited sequence depth (70,000 genomic tags per library) we were able to find novel differentially methylated loci in our mouse model. Since most of the Not I sites are correlated with a CpG Island in the genome it can be expected that the differences in tag counts as identified by MSDK correlate with changes in transcription levels, which ultimately can influence the phenotype seen in our mouse model.
Comparison between MSDK and SAGE
Methylation Specific Digital Karyotyping
Serial Analysis of Gene Expression
MSDK Genomic Tag Sequence
SAGE Tag Sequence
zinc-finger protein NOLZ1
heat shock protein 90 kDa alpha, B1
PAN3 polyA specific ribonuclease subunit
WD repeat and SOCS box-containing 2
Selected candidate genes for real-time PCR analysis
Nfatc1 (nuclear factor of activated T-cells)
Jak2 (Janus kinase 2)
Rcor3 (REST corepressor 3)
Tmem151a (Hypothetical protein LOC381199)
A quantitative MSP assay was developed for parts of a CpG Island in close proximity of the genomic tags matched to Runx3 and Nfatc1. Although this assay demonstrated an increased methylation level (10 to 50% ± 20%) in the genomic region analyzed in lung tissue and spleen, the results could be masked due to the use of a mixed cell population. Also the length of the CpG Island (over 1000 bp for Runx3) makes it difficult to design the assays. An extensive in vitro promoter analysis might be necessary to clearly identify the specific regulatory elements susceptible for methylation. Interestingly, the transcription factor Runx3 has been shown to be regulated by promoter methylation in human cancers [14, 15] and it was also shown that Runx3 can be down regulated by an increase of Histone H3 methylation in human cancer cell lines . More recently we have shown , that a demethylating agent can restore the transcription levels of Runx3 in spleen cells from HMD animals, implying that the transcriptional changes are caused by methylation changes. The expression of nuclear factor of activated T cell 1 (Nfatc1) has also been described to be regulated by hypermethylation in Hodgkin's lymphoma as well as by histone H3 acetylation and H3-K4 trimethylation . It is not known whether Rcor3 (Rest corepressor 3) it self is regulated by methylation though depletion of Corest can result in derepression of REST responsive gene expression and increased methylation of Histone H3-K4 [18, 19]. Other examples of genes regulated by methylation that have been identified in our study as differentially methylated candidate genes [see Additional files 1 and 2] can be found in the literature like Cited4, which is epigenetically silenced in the vast majority of human oligodendroglial tumors . Taken together these findings indicate that it is very likely that our list of differentially methylated loci is actually regulated by DNA methylation but it also indicates that the contribution of other epigenetic mechanisms like histone modifications affecting the accessibility of chromatin can not be excluded.
Differential gene expression and functional analysis
Perinatal dietary changes in methyl donor content can lead to alterations in expression profiles as well as subtle changes in DNA methylation. Using MSDK, a method that allows a comprehensive and unbiased genome-wide methylation profiling, we uncovered differentially methylated loci in the progeny of mice maternally subjected to diets high and low in methyl donors. The depth and coverage of the approach is dependent on the restriction enzyme used and can be adjusted as needed. The MSDK technology is sequence based, quantitative and unbiased without the requirement of special equipment other than a DNA sequencer. An increase in throughput and large reduction of the sequencing costs is expected with the recent development of multiplex paired-end ditag sequencing technologies [22, 23]. Most importantly; the data is digitally archived, relative easy to analyze and independent of an arbitrarily chosen reference. MSDK is applicable for mouse models in a mixed cell population, and may be a useful approach to determine whether environmental exposures can lead to epigenetic changes in complex heritable human diseases.
Primers and linkers
Not-MSDK linkers: 5'-/5Phos/GGCCGCACCCAACTCGATTACGAACCTCTGC-3' and 5'-/5Bio/TTTGCAGAGGTTCGTAATCGAGTTGGGTGC-3'. These linkers were obtained PAGE purified and modified from Integrated DNA Technologies, Coralville, IA.
RT-PCR primers: Jak2 Forward 5'-TCTGTGGGAGATCTGCAGTG-3', Jak2 Reverse 5'-CACGGATGACAGCTCTGAAA-3'; Nfatc1 Forward 5'-TCATCCTGTCCAACACCAAA-3', Nfatc1 Reverse 5'-TCACCCTGGTGTTCTTCCTC-3'; Rcor3 Forward 5'-CATGGATGGAAACGACAGTG-3', Rcor3 Reverse 5'-AGTTGCCTCAGGATGGTGTT-3'; B2M Forward 5'-ATTCACCCCCACTGAGACTG-3', B2M Reverse 5'-GCTATTTCTTTCTGCGTGCAT-3'; PGK1 Forward 5'-CAAGGCTTTGGAGAGTCCAG-3', PGK1 Reverse 5'-TGTGCCAATCTCCATGTTGT-3'; Actb Forward 5'-TCCGTAAAGACCTCTATGCC-3'; Actb Reverse 5'-TACTCCTGCTTGCTGATCC-3'
Tmem151a Forward 5'-AGGGCGAAGGTGGAGACT-3', Tmem151 Reverse 5'-GGCATGGATGAGCAGTGTAA-3'; mDnmt3a Forward 5'-TGACGCCAAAGAAGTGTCTG-3, mDnmt3a Reverse 5'-TTCAGTGCACCACAGGATGT-3'; mDnmt3b Forward 5'-ACTTGGTGATTGGTGGAAGC-3', mDnmt3b Reverse 5'-CCAGAAGAATGGACGGTTGT-3'; mDnmt1 Forward 5'-TCCTCAGGGACCATATCTGC-3', mDnmt1 Reverse 5'-CTGCACAGGAACAGACTCCA-3'. MSP primers: Runx3 methylated forward 5'-AGAAAATCGTTTTGGGTGTTATC-3', reverse 5'-AATTTCCAACCTCCTAACTACGAC-3'; Nfatc1 methylated forward 5'-GTAGTTTAGTTAGGGAGGAGGATTC-3', reverse 5'-TACGAAAACGAAAAAACTTTACGAC-3'; Actb methylated forward 5'-TGTGATTGATAGTAGGAAGGTGTGA-3'; reverse 5'-ACCCAAATCCAAAAATCACG-3'.
SAGE library construction and statistical analysis of tag counts differences
SAGE libraries from the same samples used for MSDK analysis were constructed using Nla III as the anchoring enzyme and BsmF I as the tagging enzyme according to a micro-SAGE protocol . The SAGE library clones were arrayed and inserts were purified and sequenced at Agencourt Bioscience Corporation. The SAGE 2000 software version 4.12 (available at http://www.sagenet.org) was used to extract SAGE tags from the original sequence files, remove duplicate ditags, remove linker sequences, remove one base pair variations of linker sequences and tabulate the occurrence of each tag. Tag sequences, tag counts and gene associations were stored in a Microsoft Access relational database for subsequent analysis. P-values for differentially expressed transcripts were calculated according to the sequence odds ratio and significant test http://cgap.nci.nih.gov/SAGE). Similar results were obtained when using the SAGE software Monte Carlo approach or the significance test available as part of the DiscoverySpace application . The generated mouse SAGE libraries have been deposit at the Geo Website (GSE11676).
Gene Ontology and Canonical Pathway analysis
Ingenuity Pathway Analysis (IPA, Ingenuity Systems®, http://www.ingenuity.com) is a web-based application that enables the visualization, discovery and analysis of molecular interaction networks within gene expression profiles. The generated SAGE datasets and the corresponding expression levels, represented as the log2 ratios, were uploaded within the IPA database for further analysis. Both gene symbols and gene bank accession numbers were used with no apparent differences in results. These genes, called focus genes, were overlaid onto a global molecular network developed from information contained in the Ingenuity knowledge base. The IPA knowledge base represents a proprietary ontology of over 600,000 classes of biologic objects spanning genes, proteins, cells and cell components, anatomy, molecular and cellular processes, and small molecules. Networks of the focus genes were then algorithmically generated based on their connectivity. The Functional Analysis of a network identified the biological functions and/or diseases that were most significant to the genes in the network. The network genes associated with biological functions and/or diseases in the Ingenuity knowledge base were considered for the analysis. Fischer's exact test was used to calculate a P-value determining the probability that each biological function and/or disease assigned to that network is due to chance alone. Canonical Pathways Analysis identified the pathways from the Ingenuity Pathways Analysis library of canonical pathways that were most significant to the dataset. The significance of the association between the dataset and the canonical pathway was measured in 2 ways: 1) a ratio of the number of genes from the dataset that map to the pathway divided by the total number of molecules that exist in the canonical pathway is displayed. 2) Fischer's Exact Test was used to calculate a P-value.
RNA isolation and real-time PCR
Total RNA was extracted from frozen lung tissue using the RNAgents total RNA isolation system (Promega, Madison, WI, USA). Equal amounts of total RNA (5 μg), as determined by the Ribo-Green RNA Quantification kit (Molecular Probes, Eugene, OR, USA), were used in a 20 μl cDNA synthesis reaction primed with oligo-dT (Superscript II; Invitrogen, Carlsbad, CA, USA). Control reactions were prepared in parallel without reverse transcriptase. Prior to cDNA synthesis, residual genomic DNA was removed from total RNA with a DNase I treatment (DNA-free; Ambion, Austin, TX, USA). Quantitative PCR was performed with a 7900TH Fast Real-Time PCR system (Applied Biosystems, Foster City, CA, USA) using SYBR-Green. PCR reactions were performed in triplicate, and the threshold cycle numbers were averaged. Gene expression levels were normalized to three genes: ACTB (actin, beta), B2M (beta-2-microglobulin and PGK1 (phosphoglycerate kinase 1). The relative expression levels were calculated in comparison to the levels in total RNA from naïve mouse brain (Ambion, Austin, TX) according to the Comparative Ct method in which the relative expression equals 2-ΔΔCt. PCR primers were designed using the Primer 3 interface http://frodo.wi.mit.edu/cgi-bin/primer3/primer3_www.cgi. Data is presented as the mean ± standard error of the mean. Significant differences between groups were identified by analysis of variance. Individual comparisons between groups were confirmed by the two-tailed Student's t test or the Mann-Whitney U Test. A P-value ≤ to 0.05 was considered significant.
Methylation Specific PCR
Sodium bisulfite modification of 500 ng genomic mouse lung DNA was performed using the EZ DNA Methylation-Gold Kit (Zymo Research, Orange, CA) according to manufacture's instructions. Modified DNA was eluted from the column with 20 ul elution buffer, aliquoted and stored at -20°C. PCR reactions were performed essentially as described using 2 ul modified genomic DNA . CpG islands at the 5' region and up to the first exon of each gene were identified using online tools http://genome.ucsc.edu/. The corresponding sequences were downloaded for primer design using MethPrimer  and Primer3 http://frodo.wi.mit.edu/cgi-bin/primer3/primer3_www.cgi. Primers were designed to contain at least one CpG dinucleotide. Amplified products were analyzed by gel electrophoresis. Data was represented as mean ± standard error of the mean. Significant differences between groups were identified by analysis of variance. Individual comparisons between groups were confirmed by the two-tailed Student's t test or the Mann-Whitney U test. A P-value = to 0.05 was considered significant.
TopoA cloning and sequencing
Amplified MSP products were analyzed by gel electrophoresis prior to further processing and purified by phenol extraction and ethanol precipitation. Approximately 70 ng of PCR product was used in a ligation reaction according to manufactures instructions using a TOPO TA cloning kit for Sequencing (Invitrogen, Carlsbad, CA). Transformants were analyzed by colony PCR with universal M13 primers. These PCR products were subsequently purified using a QIAquick PCR Purification Kit (Qiagen USA) and eluded from the columns in a 30 ul volume. For the sequencing reaction 4 ul purified PCR product with 5 pmole T7 universal primer was used in combination with a Dynamic ET Terminator Cycle Sequencing Kit (Amersham Biosciences, Piscataway, NJ). Post-sequencing cleanup was performed according to manufactures instructions.
This work was supported by NIEHS and NHLBI Intramural Research Programs (DAS) and HL091335 (JWH).
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