Lineage-specific activators affect beta-globin locus chromatin in multipotent hematopoietic progenitors

EMBO J. 2006 Aug 9;25(15):3586-95. doi: 10.1038/sj.emboj.7601232. Epub 2006 Jul 13.

Abstract

During development, the regulated expression of tissue-specific genes can be preceded by their potentiation, that is, by chromatin activation in progenitor cells. For example, the human beta-like globin genes are potentiated in a gene- and developmental-specific manner in hematopoietic progenitors. Developmental regulation of human beta-gene expression in erythroid cells is mostly determined by transcriptional activators; however, it is not clear how gene-specific potentiation is set in hematopoietic progenitors. Using human and transgenic multipotent hematopoietic progenitors, we demonstrate that human beta-globin locus activation is characterized by TBP, NF-E2, CBP and BRG1 recruitment at both the Locus Control Region and human beta-gene promoter. Our results further indicate that in hematopoietic progenitors, EKLF influences chromatin organization at the human beta-globin locus and is instrumental for human beta-gene potentiation. Thus, we show that lineage-specific transcriptional activators expressed at basal levels in progenitor cells can participate in gene potentiation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Lineage / physiology
  • Chromatin / genetics*
  • Chromatin / metabolism
  • DNA Helicases
  • Female
  • Gene Expression Regulation, Developmental*
  • Globins / genetics*
  • Globins / metabolism
  • Hematopoietic Stem Cells / metabolism*
  • Histones / metabolism
  • Humans
  • Kruppel-Like Transcription Factors / metabolism*
  • Male
  • Mice
  • Mice, Transgenic
  • Models, Biological
  • NF-E2 Transcription Factor, p45 Subunit / metabolism
  • Nuclear Proteins / metabolism
  • Promoter Regions, Genetic
  • Transcription Factors / metabolism
  • Transcriptional Activation*

Substances

  • Chromatin
  • Histones
  • Kruppel-Like Transcription Factors
  • NF-E2 Transcription Factor, p45 Subunit
  • Nuclear Proteins
  • Transcription Factors
  • erythroid Kruppel-like factor
  • Globins
  • SMARCA4 protein, human
  • Smarca4 protein, mouse
  • DNA Helicases