The TR2 and TR4 orphan nuclear receptors comprise the DNA-binding core of direct repeat erythroid definitive, a protein complex that binds to direct repeat elements in the embryonic and fetal β-type globin gene promoters. Silencing of both the embryonic and fetal β-type globin genes is delayed in definitive erythroid cells of Tr2 and Tr4 null mutant mice, whereas in transgenic mice that express dominant-negative TR4 (dnTR4), human embryonic ε-globin is activated in primitive and definitive erythroid cells. In contrast, human fetal γ-globin is activated by dnTR4 only in definitive, but not in primitive, erythroid cells, implicating TR2/TR4 as a stage-selective repressor. Forced expression of wild-type TR2 and TR4 leads to precocious repression of ε-globin, but in contrast to induction of γ-globin in definitive erythroid cells. These temporally specific, gene-selective alterations in ε- and γ-globin gene expression by gain and loss of TR2/TR4 function provide the first genetic evidence for a role for these nuclear receptors in sequential, gene-autonomous silencing of the ε- and γ-globin genes during development, and suggest that their differential utilization controls stage-specific repression of the human ε- and γ-globin genes.
ASJC Scopus subject areas
- Molecular Biology
- Biochemistry, Genetics and Molecular Biology(all)
- Immunology and Microbiology(all)