- Research article
- Open Access
Proton irradiation induces persistent and tissue-specific DNA methylation changes in the left ventricle and hippocampus
© Impey et al. 2016
Received: 14 December 2015
Accepted: 8 March 2016
Published: 31 March 2016
Proton irradiation poses a potential hazard to astronauts during and following a mission, with post-mitotic cells at most risk because they cannot dilute resultant epigenetic changes via cell division. Persistent epigenetic changes that result from environmental exposures include gains or losses of DNA methylation of cytosine, which can impact gene expression. In the present study, we compared the long-term epigenetic effects of whole body proton irradiation in the mouse hippocampus and left ventricle. We used an unbiased genome-wide DNA methylation study, involving ChIP-seq with antibodies to 5-methylcytosine (5mC) and 5-hydroxymethylcytosine (5hmC) to identify DNA regions in which methylation levels have changed 22 weeks after a single exposure to proton irradiation. We used DIP-Seq to profile changes in genome-wide DNA methylation and hydroxymethylation following proton irradiation. In addition, we used published RNAseq data to assess whether differentially methylated regions were linked to changes in gene expression.
The DNA methylation data showed tissue-dependent effects of proton irradiation and revealed significant major pathway changes in response to irradiation that are related to known pathophysiologic processes. Many regions affected in the ventricle mapped to genes involved in cardiovascular function pathways, whereas many regions affected in the hippocampus mapped to genes involved in neuronal functions. In the ventricle, increases in 5hmC were associated with decreases in 5mC. We also observed spatial overlap for regions where both epigenetic marks decreased in the ventricle. In hippocampus, increases in 5hmC were most significantly correlated (spatially) with regions that had increased 5mC, suggesting that deposition of hippocampal 5mC and 5hmC may be mechanistically coupled.
The results demonstrate long-term changes in DNA methylation patterns following a single proton irradiation, that these changes are tissue specific, and that they map to pathways consistent with tissue specific responses to proton irradiation. Further, the results suggest novel relationships between changes in 5mC and 5hmC.
Environment epigenetics is the study of how environmental exposures interact with the epigenome to cause stable epigenetic change, most notably changes in DNA methylation patterns. Environmental exposures include physical interactions, such as chemicals and radiation [1, 2], but also extend to other interactions such as emotional stress  and changes in circadian rhythms . Accumulating evidence has shown changes in genomic DNA methylation profiles (i.e., levels and/or distribution) from environmental exposures [1, 2], but how these exposures are translated to the observed DNA methylation changes are essentially unknown. Also unknown is whether these changes are physiological or pathological responses to the exposures, or a mixture of both.
DNA methylation is found in two main forms. The best characterized is 5 methylcytosine (5mC), which is associated with loss of transcription potential [3, 5]. No direct mechanism to remove the methyl group from cytosine has been demonstrated in mammals. A second form of DNA methylation is 5-hydroxymethylcytosine (5hmC), which is enzymatically derived from 5mC  by the Tet-family hydroxylases [7, 8]. The discovery of 5hmC as a modified form of 5mC changed the perception of 5mC as a stable epigenetic modification to one that may be dynamically regulated under certain conditions, including from environmental exposures . The roles of 5hmC have not been fully elucidated, but current thought is that 5hmC is involved in DNA demethylation and also plays a role in active gene expression . A reasonable presumption is that these two activities are linked at times.
Dynamic changes in DNA methylation are programmed during early development beginning with fertilization  and continue at a much lower rate after development reflecting life exposures [11–13]. Changes over the life span have reported for 5mC in human blood , nonhuman primate brain , and mouse tissues [16, 17]. The mouse studies suggested a degree of tissue-specificity [16, 17].
In the present study, we used an unbiased genome-wide DNA methylation approach to determine the extent, persistence, and tissue specificity (brain versus heart) of genomic 5mC and 5hmC changes in mice following proton irradiation, which is increasingly used in cancer therapy [18–20] and is of particular interest to NASA because protons are abundant in galactic cosmic rays and solar particle events (SPE) . The brain was chosen because proton irradiation affects this tissue in humans as part of cancer treatment [22, 23], and specifically the hippocampus was chosen because it might be especially sensitive to effects of proton irradiation [24–26]. The heart was chosen as a second tissue of interest because cardiovascular (CV) disease is a latent effect from radiotherapy in cancer patients [27, 28] and has been reported in Hiroshima and Nagasaki atomic bomb survivors [29, 30].
We report persistent changes in 5mC and 5hmC in both tissues as a result of exposure, that these changes are not distributed randomly, and they reflect both tissue specific and tissue independent responses to the proton exposure. The results also suggest that the retention versus loss of 5hmC that forms from 5mC in response to proton irradiation is not random.
DNA methylation in the left ventricle and hippocampus
DNA methylation in the left ventricle and hippocampus 22 weeks after proton irradiation
The brain is unique among differentiated tissues because many brain regions have high levels of 5hmC that persist throughout development. In particular, up to 20 % of modified CpGs have been proposed to be 5hmC in hippocampus. Our data indicate that, in contrast to what is seen in the left ventricle, the most significant spatial correlation in the hippocampus was for regions with increased 5hmC and 5mC. Thus, these data indicate that in the hippocampus 5hmC accumulation is not causally linked to local DNA methylation. The co-localization of upregulated DMRs and DHMRs is consistent with previous observations suggesting that 5hmC is an abundant and persistent mark in brain [31, 37]. Moreover, it raises the possibility that deposition of hippocampal 5mC and 5hmC may be mechanistically coupled. And finally, the overall patterns of change for the hippocampus and ventricle suggest differences in the epigenomic responses of both tissues to proton exposure.
In contrast to regions associated with decreased 5mC and 5hmC, radiation-regulated regions linked to increased 5mC and 5hmC in heart and hippocampus did not show highly significant enrichment for gene ontology categories (no categories below FDR-adjusted p < 0.02). Moreover, modestly significant gene categories were largely comprised of metabolic and general signaling pathways (e.g. regulation of transcription, regulation of RNA-metabolism, regulation of biosynethic process, G-protein signaling, cytoskeleton etc.). These results suggest that proton radiation-induced epigenetic remodeling induces a general transcriptional response.
In this study, we examined the genome-wide distribution of 5mC and 5hmC in two different tissues (left ventricle and hippocampus) from sham and proton irradiated mice using an unbiased sliding window approach to identify and merge regions enriched for these marks. Consistent with previous studies by others [38, 39], both 5hmC and 5mC-enriched regions were predominantly found in intragenic domains while 5hmC was enriched in gene bodies and at the 5 prime ends of genes. In hippocampus and ventricle, 5hmC was enriched in the gene bodies of actively transcribed genes. Interestingly, 5mC was enriched inside genes transcribed at low levels in hippocampus but not in heart. This is consistent with other studies that found global differences in methylation in brain versus blood . Results from studies involving stem cells suggest that intragenic methylation correlates with active transcription . Thus, the association of methylation with repressed genes in hippocampus suggests that this mark may have a repressive role in brain. Interestingly, intragenic methylation in brain has been linked to suppression of elongation and alternative splicing [41, 42].
We next examined the genome-wide distribution of 5mC and 5hmC relative to repetitive DNA. Both 5hmC and 5mC were detected in major repeat classes with greatest enrichment in SINEs and LINEs. These results are consistent with previous studies  and suggest that, like 5mC, 5hmC may play a role in repression of repeats and maintenance of genomic stability in these tissues. Interestingly, we observed a significant increase in 5hmC and decrease in 5mC at tRNA repeats in ventricle (relative to hippocampus) suggesting that the Tet/5hmC pathway may differentially regulate transcribed RNA repeats in the heart. Consistent with this idea, 5mC was significantly depleted at rRNA repeats in ventricle and there was a trend towards 5hmC depletion at rRNA repeats in hippocampus (p < 0.1). Similar regulation of tRNA-associated DMRs and DHRs was observed with subsets of the data indicating that epigenetic regulation of this class of repeats is global. Because regulation of tRNA transcription can regulate protein biogenesis this global epigenetic regulation may be biologically meaningful . Thus, it is possible that differential Tet-mediated oxidation of tRNA and rRNA repeats in ventricle regulates transcription of these genes and potentially protein biogenesis.
Differential methylation in response to proton radiation was examined using merged regions at an FDR-adjusted p < 0.01. Because oxidation of 5mC into 5hmC is a sequential process believed to contribute to active demethylation, we examined the overlap of these two marks in hippocampus and heart. The inverse relationship between 5hmC and 5mC in heart we observed was anticipated because 5hmC is formed from 5 mC via sequential oxidation. Likewise, coordinated downregulation of 5hmC and 5mC in the heart is consistent with active demethylation occurring. The high-degree of overlap between regions that showed increased 5hmC and 5mC in brain is surprising because it suggests an active “maintenance” process. The brain is unique because it is the only tissue where high-levels of 5hmC are maintained throughout post-natal development [38, 45, 46]. Thus, we speculate that radiation-induced increases in 5hmC are similarly stabilized via an active process. Regardless, our data show that acute radiation exposure stably remodels the heart and brain epigenomes. Future studies with single nucleotide resolution could determine the degree to which de novo deposition of 5mC and 5hmC is regulated in a coordinated fashion.
The persistent epigenomic changes we observed were not random. Gene pathway analyses of domains that showed decreased 5mC in response to proton radiation revealed striking enrichment for key tissue-specific pathways, suggesting that epigenetic remodeling was associated with cellular differentiation responses. Moreover, these pathways were highly enriched for genes that are key regulators of cell-fate identity for brain and heart, respectively. For example in heart, SRF, Nkx2-5, Myocardin, and Myocardin-like are transcriptional master-regulators of heart development and differentiation that co-regulate overlapping gene pathways [47, 48]. All showed decreased accumulation of 5mC after exposure. Further, regions with decreased 5hmC in the ventricle were also enriched for muscle and heart-specific gene pathways. Given the role of these factors in cardiomyocyte and vascular differentiation, we hypothesize that epigenetic regulation of these genes represents a radiation-induced differentiation response. Interestingly, a recent study found that Tet2 was highly expressed in heart and that deletion of Tet2 resulted in hypermethylation of Myocardin and SRF and exacerbation of cardiovascular injury .
In hippocampus, genes associated with axon growth, neuronal differentiation, neurogenesis and synaptic proteins were enriched at domains with decreased 5mC in response to radiation. These results suggest epigenetic remodeling of pathways that regulate neuronal plasticity and may represent a compensatory response to damage. Hippocampal tissue also showed enrichment for genes linked to small G-protein signaling and cytoskeletal remodeling at regions associated with increased 5hmC. The association with cytoskeletal remodeling is consistent with alterations in spine measures seen 30 days following proton irradiation  and 60 days following 56Fe irradiation .
Most importantly, our data highlight that proton irradiation generates a tissue-specific response that targets key regulators of differentiation and plasticity in heart and brain. As noted in the Introduction, ionizing radiation is just one of many forms of environmental exposures. A logical, albeit speculative, extension of our data is that other forms of environmental exposures also cause tissue-specific epigenomic responses, at least in post-mitotic cells. Presumably, in addition to tissue specific responses, exposure specific responses would also be observed because different agents and stressors induce different cellular responses. If so, our cells are repositories of exposures accumulated over a lifetime.
In summary, our data present clear evidence of tissue-dependent epigenetic effects of proton irradiation, as well as some shared effects that are consistent with a common response to radiation damage. The gene methylation data in both tissues revealed significant major pathway changes that are related to known pathophysiologic processes. The tissue-dependent results are unique in the context of response to radiation and, combined with the major pathway changes identified, support the power of this approach.
Animals and study design
Six-month-old C57BL/6J male mice (n = 10 mice) were obtained from Jackson Laboratories, Bar Harbor Maine. The mice were shipped from Jackson Laboratories to Brookhaven National Laboratory (BNL), Upton, Long Island, New York, and allowed to accommodate to the housing facility there for one week. Subsequently, the mice were irradiated with 1 Gy of 150 MeV protons or sham-irradiated. For irradiation, mice were loaded into 8 x 3 x 3 cm plastic square enclosures with air holes and placed in a foam fixture in the beam line of the NASA Space Radiation Laboratory (NSRL). They were exposed to a rectangular beam of approximately 20 x 20 cm. The focused beam of high-energy was generated by the Booster accelerator at BNL and transferred to the experimental beam line at the NSRL facility. Dose calibration was performed to ensure that the desired dose was delivered. Sham-irradiated mice were placed into the plastic enclosures for the same time as the irradiated mice. Mice were randomly assigned to the experimental groups. One week after the irradiation or sham-irradiation, the mice were shipped to Oregon Health & Science University (OHSU) and were killed by cervical dislocation for analyses 22 weeks after the irradiation date. The hippocampus of one hemibrain and left ventricle of 10 mice were divided in separate tissues for DNA methylation analyses. All protocols were reviewed and approved by the Institutional Animal Care and Use Committees (IACUC) of OHSU and BNL and were in compliance with all Federal regulations.
DNA methylation sequencing
DNA was isolated from the left ventricle and hippocampus. Antibodies against 5mC and 5hmC were used to immunoprecipitate DNA preparations for methyl-DNA immunoprecipitation (meDIP) and hydroxymethyl-DNA immuno precipitation, respectively, from eight pools of tissues (2 x 2 pools of hippocampal tissues and 2 x 2 pools of left ventricle tissues, or 2 pools/tissue/radiation condition) (see Fig. 1 for a diagram of the protocol). The antibodies used against 5mC and 5hmC do not cross react. These antibodies were used to precipitate genomic regions that are enriched for either 5mC or 5hmC. Following immunoprecipitation, high throughput genomic sequencing was used to identify these enriched genomic regions. For DIP-Seq library preparation, RNAse-treated DNA was isolated using the Qiagen Allprep DNA/RNA protocol. The DNA was sonicated using a Cole Parmer CPX-132 sonicator (75 % amplitude, 3x10’) and polished using the DNA terminator end repair kit (Lucigen). DNA fragments were A-tailed using Klenow exo-(Epicenter) and ligated to un-methylated HT TrueSeq indexed adapters and purified. The resulting purified DNA was denatured at 95 C, resuspended in 100 ul of DIP IP buffer, and immunoprecipitated with 1 μg of the highly specific 5-methylcytosine antibody (Eurogentec) or 2 ul of 5-hydroxymethylcytosine (Active Motif) antibody and Dynal anti-mouse IgG beads. Beads were rinsed 7 times with IP buffer, eluted with 1 % SDS at room temperature and the eluted DNA is purified and subjected to limited amplification (~18 cycles). Libraries were sequenced on the HiSeq2000 platform at the OHSU Massively Parallel Sequencing Shared Resource or the Oregon State University Center for Genome Research and Biocomputing.
Bioinformatics and statistics
35 bp single read sequence data was mapped to the mouse reference genome (UCSC mm9) using the Bowtie algorithm using standard flags and allowing 2 mismatches . Sequences that map to a single location were selected and domains enriched for 5mC or 5hmC were selected using a parameter-optimized Monte-Carlo-based segmentation algorithm . A 1000 bp sliding-window was used based on iterative analyses that maximized the number of enriched regions. A comparison of different high-throughput sequencing based methods to study DNA methylation concluded that MeDIP-Seq covers ~ 67 % of genomic CpGs .
For statistical comparisons of biological samples, regions of methylation enrichment were merged and differences in methylation interrogated with FDR-adjusted chi-square or negative binomial statistics . Statistical and visualization studies involved the R programming language and Bioconductor packages . Gene ontology analyses utilized the bioconductor Goseq package, which adjusts for RNA-Seq length bias artifacts . For gene ontology analyses the top 2000 DMRs or DHRs (FDR-adjusted p < 0.01) within 50kb of a transcriptional start site were non-redundantly annotated. Pathway analyses involved standard bioconductor packages (e.g. cmap, keggraph, gsea). DIP sequence-tag heatmaps were generated in R by plotting median-normalized DIP-Seq tag density in gene bodies and indicated flanking regions with color-maps scaled to the 80 % quantile. Statistical analyses of pathway data were conducted via FDR-adjusted Fisher exact or KS-tests. We considered p < 0.05 as statistically significant.
None of the authors has competing financial interests or other conflicts of interest. We thank Peter Guida, Adam Rusek, and other NSRL physics staffs for their invaluable help at BNL. We also thank Dr. Robert Searles, the Director of the Massively Parallel Sequencing Shared Resource and Associate Director Integrated Genomics Laboratory at OHSU, for providing his expertise for the design and interpretation of the DNA methylation and RNAseq experiments in this study. This work was supported by NASA grant NNJ12ZSA001N. All authors confirm that they have no conflict of interest to report
NASA; Grant Number: NNJ12ZSA001N
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