C9orf72 promoter hypermethylation is reduced while hydroxymethylation is acquired during reprogramming of ALS patient cells

Exp Neurol. 2016 Mar:277:171-177. doi: 10.1016/j.expneurol.2015.12.022. Epub 2015 Dec 31.

Abstract

Among several genetic mutations known to cause amyotrophic lateral sclerosis (ALS), a hexanucleotide repeat expansion in the C9orf72 gene is the most common. In approximately 30% of C9orf72-ALS cases, 5-methylcytosine (5mC) levels within the C9orf72 promoter are increased, resulting in a modestly attenuated phenotype. The developmental timing of C9orf72 promoter hypermethylation and the reason why it occurs in only a subset of patients remain unknown. In order to model the acquisition of C9orf72 hypermethylation and examine the potential role of 5-hydroxymethylcytosine (5hmC), we generated induced pluripotent stem cells (iPSCs) from an ALS patient with C9orf72 promoter hypermethylation. Our data show that 5mC levels are reduced by reprogramming and then re-acquired upon neuronal specification, while 5hmC levels increase following reprogramming and are highest in iPSCs and motor neurons. We confirmed the presence of 5hmC within the C9orf72 promoter in post-mortem brain tissues of hypermethylated patients. These findings show that iPSCs are a valuable model system for examining epigenetic perturbations caused by the C9orf72 mutation and reveal a potential role for cytosine demethylation.

Keywords: Amyotrophic lateral sclerosis; C9orf72; Cytosine hydroxymethylation; Repeat expansion.

Publication types

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

MeSH terms

  • 5-Methylcytosine / metabolism
  • Amyotrophic Lateral Sclerosis / genetics*
  • Amyotrophic Lateral Sclerosis / pathology*
  • Brain / pathology
  • C9orf72 Protein
  • Coculture Techniques
  • CpG Islands / physiology
  • Cytosine / analogs & derivatives
  • DNA Methylation / genetics
  • Green Fluorescent Proteins / genetics
  • Green Fluorescent Proteins / metabolism
  • Homeodomain Proteins / metabolism
  • Humans
  • Induced Pluripotent Stem Cells / physiology*
  • Lymphocytes / physiology
  • Motor Neurons / physiology
  • Mutation / genetics*
  • Nanog Homeobox Protein
  • Nestin / metabolism
  • Promoter Regions, Genetic / physiology*
  • Proteins / genetics*
  • RNA, Messenger / metabolism
  • SOXB1 Transcription Factors / metabolism
  • Time Factors

Substances

  • C9orf72 Protein
  • C9orf72 protein, human
  • Homeodomain Proteins
  • NANOG protein, human
  • Nanog Homeobox Protein
  • Nestin
  • Proteins
  • RNA, Messenger
  • SOX2 protein, human
  • SOXB1 Transcription Factors
  • 5-hydroxymethylcytosine
  • Green Fluorescent Proteins
  • 5-Methylcytosine
  • Cytosine