A novel erythroid differentiation related gene EDRF1 upregulating globin gene expression in HEL cells

Chin Med J (Engl). 2002 Nov;115(11):1701-5.

Abstract

Objective: To further characterize the differentiation inducing properties of EDRF1 and demonstrate its functional pathway involved in regulation of globin gene expression.

Methods: By transfecting EDRF1 sense and antisense constructs into HEL cells, we identified the expression of globin and erythropoietin receptor genes by Northern blot analysis. RT-PCR and EMSA (electrophoresis mobility shift assay) were performed to monitor the expression and DNA-binding activity of erythroid specific transcription factors GATA-1 and NF-E2.

Results: It was shown that when EDRF1 was overexpressed, production of alpha-globin increased. In antisense EDRF1, overexpression of HEL cells, significant loss of alpha-, gamma-globin mRNA synthesis was observed. The transcription of endogenous GATA-1 and NF-E2 mRNA expression were maintained at the same levels compared with control experiments. However, the transcription activity of GATA-1 was severely impaired. Expression of erythropoietin receptor gene was not influenced by EDRF1 gene overexpression.

Conclusion: The results suggested that EDRF1 regulated alpha- and gamma-globin gene synthesis by modulating DNA-binding activity of GATA-1 transcription factor.

MeSH terms

  • Cell Differentiation
  • Cells, Cultured
  • DNA-Binding Proteins / genetics
  • Erythroid-Specific DNA-Binding Factors
  • Erythropoiesis / physiology*
  • GATA1 Transcription Factor
  • Gene Expression Regulation*
  • Globins / genetics*
  • Humans
  • NF-E2 Transcription Factor
  • NF-E2 Transcription Factor, p45 Subunit
  • RNA, Messenger / analysis
  • Transcription Factors / genetics
  • Up-Regulation

Substances

  • DNA-Binding Proteins
  • Erythroid-Specific DNA-Binding Factors
  • GATA1 Transcription Factor
  • GATA1 protein, human
  • NF-E2 Transcription Factor
  • NF-E2 Transcription Factor, p45 Subunit
  • NFE2 protein, human
  • RNA, Messenger
  • Transcription Factors
  • Globins