DNA methylation and human disease

Nat Rev Genet. 2005 Aug;6(8):597-610. doi: 10.1038/nrg1655.

Abstract

DNA methylation is a crucial epigenetic modification of the genome that is involved in regulating many cellular processes. These include embryonic development, transcription, chromatin structure, X chromosome inactivation, genomic imprinting and chromosome stability. Consistent with these important roles, a growing number of human diseases have been found to be associated with aberrant DNA methylation. The study of these diseases has provided new and fundamental insights into the roles that DNA methylation and other epigenetic modifications have in development and normal cellular homeostasis.

Publication types

  • Research Support, U.S. Gov't, P.H.S.
  • Review

MeSH terms

  • DNA Methylation*
  • Genetic Diseases, Inborn / genetics*
  • Genomic Imprinting / genetics*
  • Genomic Instability / genetics*
  • Humans
  • Neoplasms / genetics*
  • Neoplasms / metabolism