X chromosome inactivation and autoimmunity

Clin Rev Allergy Immunol. 2010 Aug;39(1):20-9. doi: 10.1007/s12016-009-8167-5.

Abstract

Autoimmune diseases appear to have multiple contributing factors including genetics, epigenetics, environmental factors, and aging. The predominance of females among patients with autoimmune diseases suggests possible involvement of the X chromosome and X chromosome inactivation. X chromosome inactivation is an epigenetic event resulting in multiple levels of control for modulation of the expression of X-linked genes in normal female cells such that there remains only one active X chromosome in the cell. The extent of this control is unique among the chromosomes and has the potential for problems when regulation is disrupted. Here we discuss the X chromosome inactivation process and how the X chromosome and X chromosome inactivation may be involved in development of autoimmune disorders.

Publication types

  • Review

MeSH terms

  • Animals
  • Autoimmune Diseases / genetics*
  • Autoimmune Diseases / immunology
  • Autoimmune Diseases / metabolism
  • Chromosomes, Human, X* / immunology
  • DNA Methylation
  • Disease Susceptibility
  • Female
  • Gene Silencing / immunology
  • Granulomatous Disease, Chronic / genetics
  • Humans
  • Hydrolases / immunology
  • Hydrolases / metabolism
  • Protein-Arginine Deiminase Type 4
  • Sex Chromosome Disorders / genetics*
  • Sex Chromosome Disorders / immunology
  • Sex Chromosome Disorders / metabolism
  • Sex Factors
  • Signal Transduction / immunology
  • Spermine / immunology
  • X Chromosome Inactivation*

Substances

  • Spermine
  • Hydrolases
  • Protein-Arginine Deiminase Type 4