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Gene Expression

Convergence of Protein Kinase C and JAK-STAT Signaling on Transcription Factor GATA-4

, , , , , & show all
Pages 9829-9844 | Received 21 Mar 2005, Accepted 10 Aug 2005, Published online: 27 Mar 2023
 

Abstract

Angiotensin II (AII), a potent vasoactive hormone, acts on numerous organs via G-protein-coupled receptors and elicits cell-specific responses. At the level of the heart, AII stimulation alters gene transcription and leads to cardiomyocyte hypertrophy. Numerous intracellular signaling pathways are activated in this process; however, which of these directly link receptor activation to transcriptional regulation remains undefined. We used the atrial natriuretic factor (ANF) gene (NPPA) as a marker to elucidate the signaling cascades involved in AII transcriptional responses. We show that ANF transcription is activated directly by the AII type 1 receptor and precedes the development of myocyte hypertrophy. This response maps to STAT and GATA binding sites, and the two elements transcriptionally cooperate to mediate signaling through the JAK-STAT and protein kinase C (PKC)-GATA-4 pathways. PKC phosphorylation enhances GATA-4 DNA binding activity, and STAT-1 functionally and physically interacts with GATA-4 to synergistically activate AII and other growth factor-inducible promoters. Moreover, GATA factors are able to recruit STAT proteins to target promoters via GATA binding sites, which are sufficient to support synergy. Thus, STAT proteins can act as growth factor-inducible coactivators of tissue-specific transcription factors. Interactions between STAT and GATA proteins may provide a general paradigm for understanding cell specificity of cytokine and growth factor signaling.

ACKNOWLEDGMENTS

This work was supported by grants from the Canadian Institutes of Health Research (MGP-13056 and MOP36382) and Génome-Québec. H.W. is the recipient of an AstraZeneca Canada/HSFC Research Fellowship, and M.N. holds a Canada Research Chair in Molecular Biology.

We thank S. Karnik, D. Richard, and T. Hoang for sharing various DNA vectors, Walter G. Thomas for generously providing the adenovirus AT1aR vector, Lise Laroche for secretarial assistance, and the Nemer Lab for helpful discussions.

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