Genomic DNA was isolated using previously published methods [20]. Animals were chosen through an extensive screening process in which gene expression and histology were measured, and the best representatives from each group were used for sequencing. Complementary MeDIP-seq and MRE-seq were then performed using previously published protocols [20]. Briefly, MeDIP utilizes antibodies against 5-methylcytidine to quantify methylated DNA sequences, while MRE-seq uses restriction enzymes that cut at unmethylated CpG sites. MeDIP-seq provides better coverage and MRE-seq offers superior resolution, so that when combined the methylome can be quantified with high accuracy [21,22]. Antibodies, restriction enzymes, DNA fragmentation, and library preparation procedures have been detailed by Li et al. [23].
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