Different sequence requirements for expression in erythroid and megakaryocytic cells within a regulatory element upstream of the GATA-1 gene

Paresh Vyas, Micheal A. McDevitt, Alan B. Cantor, Samuel G. Katz, Yuko Fujiwara, Stuart H. Orkin

Research output: Contribution to journalArticle

Abstract

The lineage-restricted transcription factor GATA-1 is required for differentiation of erythroid and megakaryocytic cells. We have localized a 317 base pair cis-acting regulatory element, HS I, associated with a hematopoietic-specific DNase I hypersensitive site, which lies approx. 3.7 kilobases upstream of the murine hematopoietic-specific GATA-1 IE promoter. HS I directs high-level expression of reporter GATA-1/lacZ genes to primitive and definitive erythroid cells and megakaryocytes in transgenic mice. Comparative sequence analysis of HS I between human and mouse shows approx. 63% nucleotide identity with a more conserved core of 169 base pairs (86% identity). This core contains a GATA site separated by 10 base pairs from an E-box motif. The composite motif binds a multi-protein hematopoietic-specific transcription factor complex which includes GATA-1, SCL/tal-1, E2A, Lmo2 and Ldb-1. Point mutations of the GATA site abolishes HS I function, whereas mutation of the E-box motif still allows reporter gene expression in both lineages. Strict dependence of HS I activity on a GATA site implies that assembly of a protein complex containing a GATA-factor, presumably GATA-1 or GATA-2, is critical to activating or maintaining its function. Further dissection of the 317 base pair region demonstrates that, whereas all 317 base pairs are required for expression in megakaryocytes, only the 5' 62 base pairs are needed for erythroid-specific reporter expression. These findings demonstrate differential lineage requirements for expression within the HS I element.

Original languageEnglish (US)
Pages (from-to)2799-2811
Number of pages13
JournalDevelopment
Volume126
Issue number12
StatePublished - Jun 1999
Externally publishedYes

Fingerprint

Erythroid Cells
Base Pairing
E-Box Elements
GATA Transcription Factors
Genes
Megakaryocytes
Lac Operon
Deoxyribonuclease I
Reporter Genes
Point Mutation
Transgenic Mice
Sequence Analysis
Dissection
Proteins
Transcription Factors
Nucleotides
Gene Expression
Mutation

Keywords

  • Cell lineage
  • Cis-elements
  • GATA-1
  • Hematopoiesis
  • Mouse
  • Transcriptional regulation

ASJC Scopus subject areas

  • Anatomy
  • Cell Biology

Cite this

Vyas, P., McDevitt, M. A., Cantor, A. B., Katz, S. G., Fujiwara, Y., & Orkin, S. H. (1999). Different sequence requirements for expression in erythroid and megakaryocytic cells within a regulatory element upstream of the GATA-1 gene. Development, 126(12), 2799-2811.

Different sequence requirements for expression in erythroid and megakaryocytic cells within a regulatory element upstream of the GATA-1 gene. / Vyas, Paresh; McDevitt, Micheal A.; Cantor, Alan B.; Katz, Samuel G.; Fujiwara, Yuko; Orkin, Stuart H.

In: Development, Vol. 126, No. 12, 06.1999, p. 2799-2811.

Research output: Contribution to journalArticle

Vyas, P, McDevitt, MA, Cantor, AB, Katz, SG, Fujiwara, Y & Orkin, SH 1999, 'Different sequence requirements for expression in erythroid and megakaryocytic cells within a regulatory element upstream of the GATA-1 gene', Development, vol. 126, no. 12, pp. 2799-2811.
Vyas, Paresh ; McDevitt, Micheal A. ; Cantor, Alan B. ; Katz, Samuel G. ; Fujiwara, Yuko ; Orkin, Stuart H. / Different sequence requirements for expression in erythroid and megakaryocytic cells within a regulatory element upstream of the GATA-1 gene. In: Development. 1999 ; Vol. 126, No. 12. pp. 2799-2811.
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