The inactivation of the π gene in chicken erythroblasts of adult lineage is not mediated by packaging of the embryonic part of the α-globin gene domain into a repressive heterochromatin-like structure

Epigenetics. 2011 Dec;6(12):1481-8. doi: 10.4161/epi.6.12.18215.

Abstract

The developmental switch of globin gene expression is a characteristic feature of vertebrate organisms. The switch of β-globin expression is believed to depend on reconfiguration of the active chromatin hub, which contains transcribed genes and regulatory elements. Mechanisms controlling the switch of α-globin gene expression are less clear. Here, we studied the mode of chromatin packaging of the chicken α-globin gene domain in red blood cells (RBCs) of primitive and definite lineages and the spatial configuration of this domain in RBCs of primitive lineage. It has been demonstrated that RBCs of primitive lineage already contain the adult-type active chromatin hub but the embryonal α-type globin π gene is not recruited to this hub. Distribution of active and repressive histone modifications over the α-globin gene domain in RBCs of definite and primitive lineages does not corroborate the hypothesis that inactivation of the π gene in RBCs of adult lineage is mediated via formation of a local repressed chromatin domain. This conclusion is supported by the demonstration that in chicken erythroblasts of adult lineage, the embryonal and adult segments of the α-globin gene domain show similar elevated sensitivities to DNase I.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Lineage
  • Chick Embryo
  • Chickens / genetics*
  • Chromatin Assembly and Disassembly
  • CpG Islands / genetics
  • DNA Methylation
  • DNA Packaging*
  • Deoxyribonuclease I / chemistry
  • Embryonic Development / genetics
  • Erythroblasts / metabolism*
  • Erythrocytes / metabolism
  • Gene Expression Regulation, Developmental*
  • Gene Silencing*
  • Heterochromatin / genetics
  • Histones / genetics
  • Histones / metabolism*
  • Nucleic Acid Conformation
  • zeta-Globins / genetics*

Substances

  • Heterochromatin
  • Histones
  • zeta-Globins
  • Deoxyribonuclease I