Role of AP1/NFE2 binding sites in endogenous alpha-globin gene transcription

Blood. 2003 Dec 1;102(12):4223-8. doi: 10.1182/blood-2003-02-0574. Epub 2003 Aug 14.

Abstract

High-level alpha-globin expression depends on cis-acting regulatory sequences located far upstream of the alpha-globin cluster. Sequences that contain the alpha-globin positive regulatory element (PRE) activate alpha-globin expression in transgenic mice. The alpha-globin PRE contains a pair of composite binding sites for the transcription factors activating protein 1 and nuclear factor erythroid 2 (AP1/NFE2). To determine the role of these binding sites in alpha-globin gene transcription, we mutated the AP1/NFE2 sites in the alpha-globin PRE in mice. We replaced the AP1/NFE2 sites with a neomycin resistance gene (neo) that is flanked by LoxP sites (floxed). Mice with this mutation exhibited increased embryonic death and alpha-thalassemia intermedia. Next, we removed the neo gene by Cre-mediated recombination, leaving a single LoxP site in place of the AP1/NFE2 sites. These mice were phenotypically normal. However, alpha-globin expression, measured by allele-specific RNA polymerase chain reaction (PCR), was decreased 25%. We examined the role of the hematopoietic-restricted transcription factor p45Nfe2 in activating expression through these sites and found that it is not required. Thus, we have demonstrated that AP1/NFE2 binding sites in the murine alpha-globin PRE contribute to long-range alpha-globin gene activation. The proteins that mediate this effect remain to be determined.

Publication types

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

MeSH terms

  • Animals
  • Archaeal Proteins*
  • Binding Sites / genetics
  • Binding Sites / physiology
  • Bone Marrow / metabolism
  • DNA-Binding Proteins / physiology*
  • Embryo, Mammalian
  • Erythrocyte Indices
  • Erythrocytes / metabolism
  • Erythroid-Specific DNA-Binding Factors
  • Gene Expression Regulation
  • Globins / genetics*
  • Liver / metabolism
  • Mice
  • Mutagenesis, Site-Directed
  • NF-E2 Transcription Factor, p45 Subunit
  • Ribosomal Proteins / chemistry*
  • Ribosomal Proteins / genetics
  • Ribosomal Proteins / physiology
  • Transcription Factors / physiology*
  • Transcription, Genetic*
  • Transcriptional Activation

Substances

  • Archaeal Proteins
  • DNA-Binding Proteins
  • Erythroid-Specific DNA-Binding Factors
  • NF-E2 Transcription Factor, p45 Subunit
  • Nfe2 protein, mouse
  • Ribosomal Proteins
  • Transcription Factors
  • ribosomal protein HS26, Haloarcula marismortui
  • Globins