DNA methylation in demyelinated multiple sclerosis hippocampus

Sci Rep. 2017 Aug 18;7(1):8696. doi: 10.1038/s41598-017-08623-5.

Abstract

Multiple Sclerosis (MS) is an immune-mediated demyelinating disease of the human central nervous system (CNS). Memory impairments and hippocampal demyelination are common features in MS patients. Our previous data have shown that demyelination alters neuronal gene expression in the hippocampus. DNA methylation is a common epigenetic modifier of gene expression. In this study, we investigated whether DNA methylation is altered in MS hippocampus following demyelination. Our results show that mRNA levels of DNA methyltransferase were increased in demyelinated MS hippocampus, while de-methylation enzymes were decreased. Comparative methylation profiling identify hypo-methylation within upstream sequences of 6 genes and hyper-methylation of 10 genes in demyelinated MS hippocampus. Genes identified in the current study were also validated in an independent microarray dataset generated from MS hippocampus. Independent validation using RT-PCR revealed that DNA methylation inversely correlated with mRNA levels of the candidate genes. Queries across cell-specific databases revealed that a majority of the candidate genes are expressed by astrocytes and neurons in mouse and human CNS. Taken together, our results expands the list of genes previously identified in MS hippocampus and establish DNA methylation as a mechanism of altered gene expression in MS hippocampus.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aged
  • Animals
  • CpG Islands / genetics
  • DNA (Cytosine-5-)-Methyltransferases / metabolism
  • DNA Methylation / genetics*
  • Demyelinating Diseases / genetics*
  • Demyelinating Diseases / pathology
  • Female
  • Hippocampus / pathology*
  • Humans
  • Male
  • Mice
  • Middle Aged
  • Multiple Sclerosis / genetics*
  • Myelin Sheath / metabolism
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • Transcription Initiation Site

Substances

  • RNA, Messenger
  • DNA (Cytosine-5-)-Methyltransferases