ARROYO DANIELA SOLEDAD
Congresos y reuniones científicas
Título:
“LA FOSFORILACIÓN INDUCIDA POR PKC REGULA LA UNIÓN DE ZFHEP A SUS PROMOTORES”.
Autor/es:
ARROYO D, ALLIER S, KNUBEL C, MALDONADO N, DARLING D.S & CABANILLAS A.M.
Lugar:
Villa Giardino, Córdoba
Reunión:
Congreso; XV Jornada Científica de la Sociedad de Biología de Córdoba; 2005
Institución organizadora:
Sociedad de Biología de Córdoba
Resumen:
REGULATION OF ZFHEP BINDING BY PKC-INDUCED PHOSPHORYLATION Arroyo D, Allier M., Knübel C, Maldonado N., Darling D.S†. & Cabanillas, A.M. CIBICI-CONICET, Facultad de Ciencias Químicas, Universidad Nacional de Córdoba.†University of Louisville, KY, USA. The activity of a transcription factor (TF) can be controlled, for instance by post-translational modification such as phosphorylation. Zfhep (Zinc Finger Homeodomain Enhancer-binding Protein) is a TF involved in lymphopoiesis, neurogenesis and myogenesis and it is expressed as two isoforms, Zfhep -1 and -2 which lacks the N-terminal DNA-binding domain of the larger Zfhep-1. Zfhep exists as two phosphorylated forms. Our goal was to examine the effect of phosphorylation on Zfhep binding to its promoters. Zfhep expressing cell lines were treated with 10 ng/ml phorbol esters (PMA) and 500 ng/ml ionomycin (IO) for 30 min. Nuclear extracts (NE) from untreated cells were incubated with calf intestinal phosphatase (CIP) or with CIP + phosphate. Band shift assays were performed with Jurkat/CHO-K1/COS-7 NE (CIP, CIP+phosphate or PMA/IO treated) and Zfhep-2 programmed rabbit reticulocyte lysates in the presence of [P]-labeled oligonucleotides harboring Zfhep binding sites from Zfhep, alfa4integrin, CD4 and p73 promoters. Probes and NE were incubated for 1 h at 20ºC. CIP- treated samples have an increased binding capacity to all the probes assayed. Retardation complexes were competed by either anti-Zfhep antibodies or an excess of cold probe. PMA/IO- treated cells shown no band of retardation. The results show that phosphorylation changes the affinity of Zfhep for its physiologically important target genes. Zfhep activity can be regulated by a signaling pathway such as PKC. It is possible that such a modification may modulate the activity of Zfhep under different conditions of cell development.