Abstract
DNA methylation is a heritable modification of genomic DNA central to development, imprinting, transcriptional regulation, chromatin structure, and overall genomic stability. Aberrant DNA methylation of individual genes is a hallmark of cancer and has been shown to play an important role in neurological disorders such as Rett syndrome. Here, we asked whether normal DNA methylation might distinguish individual brain regions. We determined the quantitative DNA methylation levels of 1,505 CpG sites representing 807 genes with diverse functions, including proliferation and differentiation, previously shown to be implicated in human cancer. We initially analyzed 76 brain samples representing cerebral cortex (n=35), cerebellum (n=34), and pons (n=7), along with liver samples (n=3) from 43 individuals. Unsupervised hierarchical analysis showed clustering of 33 of 35 cerebra distinct from the clustering of 33 of 34 cerebella, 7 of 7 pons, and all 3 livers. By use of comparative marker selection and permutation testing, 156 loci representing 118 genes showed statistically significant differences--a >or=17% absolute change in DNA methylation (P<.004)--among brain regions. These results were validated for all six genes tested in a replicate set of 57 samples. Our data suggest that DNA methylation signatures distinguish brain regions and may help account for region-specific functional specialization.
MeSH Terms
Adolescent
Adult
Aged
Brain/physiology
Brain Neoplasms/genetics
CpG Islands/genetics
DNA/genetics,isolation & purification
DNA Methylation
Female
Humans
Liver/physiology
Male
Middle Aged
Pedigree
Polymorphism, Single Nucleotide
Authors & Affiliations
10 authors, click to expand affiliations / ORCID
Ladd-Acosta Christine
Center for Epigenetics, Johns Hopkins University School of Medicine, Baltimore, MD 21287, USA.
Pevsner Jonathan
Sabunciyan Sarven
Yolken Robert H
Webster Maree J
Dinkins Tiffany
Callinan Pauline A
Fan Jian-Bing
Potash James B
Feinberg Andrew P
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