J Biol Chem, Vol. 274, Issue 35, 24449-24452, August 27, 1999

COMMUNICATION
GRF, a Novel Regulator of Calcium Signaling, Is Expressed in Pancreatic Beta Cells and Brain

Yoav Arava, Rony Seger^§, and Michael D. Walker

From the  Department of Biological Chemistry and the ^§ Department of Biological Regulation, Weizmann Institute of Science, Rehovot, Israel 76100

By screening for genes expressed differentially in pancreatic beta cells, we have isolated a cDNA encoding GRF, a novel 178-amino acid protein whose N terminus is identical to that of GRF1, a calcium-dependent guanine nucleotide exchange factor, and whose C terminus is unrelated to known proteins. We show that both GRF1 and GRF are expressed selectively in beta cell lines, pancreatic islet cells and brain. Treatment of beta cell lines (TC1 and HIT) with calcium ionophore led to a significant elevation in activity of the Ras signal transduction pathway, as determined by phosphorylation of extracellular signal-related kinase (ERK). Transfection of beta cells with a plasmid encoding a dominant negative variant of GRF1 led to 70% reduction in ERK phosphorylation, consistent with a role for GRF1 in calcium-dependent Ras signaling in these cells. To examine the possible function of GRF, cultured cells were transfected with a GRF expression vector. This led to a significant reduction in both GRF1-dependent ERK phosphorylation and AP1-dependent reporter gene activity. The results suggest that GRF1 plays a role in mediating calcium-dependent signal transduction in beta cells and that GRF represents a novel dominant negative modulator of Ras signaling.