Cooperation and Competition between the Binding of COUP-TFII and NF-Y on Human ε- and γ-Globin Gene Promoters

Chiara Liberati, Maria Rosaria Cera, Paola Secco, Claudio Santoro, Roberto Mantovani, Sergio Ottolenghi, Antonella Ronchi

Research output: Contribution to journalArticlepeer-review


The nuclear receptor COUP-TFII was recently shown to bind to the promoter of the ε- and γ-globin genes and was identified as the nuclear factor NF-E3. Transgenic experiments and genetic evidence from humans affected with hereditary persistence of fetal hemoglobin suggest that NF-E3 may be a repressor of adult ε and γ expression. We show that, on the ε-promoter, recombinant COUP-TFII binds to two sites, the more downstream of which overlaps with an NF-Y binding CCAAT box. Binding occurs efficiently to either the 5′ or the 3′ COUP-TFII site but not to both sites simultaneously. However, adding recombinant NF-Y induces the formation of a stable COUP-TFII·NF-Y-promoter complex at concentrations of COUP-TFII that would not give significant binding in the absence of NF-Y. Mutations of the promoter indicate that COUP-TFII cooperates with NF-Y when bound to the 5′ site, whereas binding at the 3′ site is mutually exclusive. Likewise, in the γ-promoter, COUP-TFII binds to a site overlapping the distal member of a duplicated CCAAT box, competing with NF-Y binding. Transfections in K562 cells show that both the mutation of the 5′ COUP-TFII or of the NF-Y site on the ε-promoter decrease the activity of a luciferase reporter; the mutation of the 3′ COUP-TFII site has little effect. These results, together with transgenic experiments suggesting a repressive activity of COUP-TFII on the ε-promoter and the observation that, on the 3′ site, COUP-TFII and NF-Y binding is mutually exclusive, suggest that COUP-TFII may exert different effects on ε transcription depending on whether it binds to the 5′ or to the 3′ site. At the 5′ site, COUP-TFII might cooperate with NF-Y, forming a stable complex, and stimulate transcription; at the 3′ site, COUP-TFII might compete for binding with NF-Y and, directly or indirectly, decrease gene activity.

Original languageEnglish
Pages (from-to)41700-41709
Number of pages10
JournalJournal of Biological Chemistry
Issue number45
Publication statusPublished - Nov 9 2001

ASJC Scopus subject areas

  • Biochemistry


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