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Nucleic Acids Research, 1988, Vol. 16, No. 10 4299-4313
© 1988


Articles

An erythroid specific nuclear factor binding to the proximal CACCC box of the ß-globin gene promoter

Roberto Mantovani1, Nicoletta Malgaretti1, Silvia Nicolis1, Barbara Giglioni2, Paola Comi2,3, Nica Cappellini4, Maria Tiziana Bertero5, Federico Caligaris-Cappio5 and Sergio Ottolenghi1,2

1Dipartimento di Genetica e di Biologia dei Microrganismi, Università di Milano Italy 2Centro sullo Studio della Patologia Cellulare, CNR, Milano Italy 3Istituto di Patologia Generale, Università di Milano Italy 4Istituto di Medicina Interna, Università di Milano Italy 5Dipartimento di Scienze Biomediche e Oncologia Umana, Università di Torino Italy

Received March 1, 1988. Revised April 22, 1988. Accepted April 22, 1988.

We have used the gel retardation and DNAase I assays to investigate the binding of nuclear proteins to the human ß-globin promoter. Upon incubation with ß-globin promoter fragments containing the duplicated CACCC boxes, nuclear proteins from human erythroid cells generate complexes yielding four retarded bands in acrylamide gels; the three slowest bands are common to both erythroid and non erythroid cells. The fast band is present only in K562 erythroleukemic cells induced to differentiation and hemogloblin accumulation and in fetal and adult erythroblasts, but absent in uninduced K562 cells. Binding occurs on a short DNA region including the proximal CACCC box, and is not significantly competed by excess {gamma}-globin fragments containing the CACCC box; the CACCC box appears to be essential for this binding, as shown by the failure of a fragment containing a natural ß-thalassemic mutation (–87, C >G) to bind significantly to nuclear factors. These data suggest that the erythroid specific CACCC binding factor might play a role in the developmental activation of ß-globin transcription.


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