Abstract

The functional interaction between the human ε globin promoter and an erythroid-specific transcription enhancer, 5′ HS-2, has been analyzed by transient expression assay. While stepwise deletion of DNA sequences between −852 and −122 had only small effects, removal of the CACC box at position −111 greatly decreased ε-globin promoter activity, as well as its response to the enhancer function of 5′ HS-2 in erythroid cells. Our data demonstrated that the three ubiquitous promoter elements, the CACC, CCAAT, and TATA boxes, of the ε-globin-encoding gene together form a minimal promoter that would interact efficiently with 5′ HS-2, and that at least the CACC box is an essential functional component of this enhancer-promoter interaction.

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