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J Biol Chem, Vol. 274, Issue 28, 19985-19991, July 9, 1999

A Cytoskeletal Localizing Domain in the Cyclase-associated Protein, CAP/Srv2p, Regulates Access to a Distant SH3-binding Site

Jong YuDagger , Christopher WangDagger , Stephen J. Palmieri§, Brian K. Haarer§, and Jeffrey FieldDagger

From the Dagger  Department of Pharmacology, University of Pennsylvania School of Medicine, Philadelphia, Pennsylvania 19104 and the § Section of Cell and Developmental Biology, University of Texas, Austin, Texas 78712

In the yeast, Saccharomyces cerevisiae, adenylyl cyclase consists of a 200-kDa catalytic subunit (CYR1) and a 70-kDa subunit (CAP/SRV2). CAP/Srv2p assists the small G protein Ras to activate adenylyl cyclase. CAP also regulates the cytoskeleton through an actin sequestering activity and is directed to cortical actin patches by a proline-rich SH3-binding site (P2). In this report we analyze the role of the actin cytoskeleton in Ras/cAMP signaling. Two alleles of CAP, L16P(Srv2) and R19T (SupC), first isolated in genetic screens for mutants that attenuate cAMP levels, reduced adenylyl cyclase binding, and cortical actin patch localization. A third mutation, L27F, also failed to localize but showed no loss of either cAMP signaling or adenylyl cyclase binding. However, all three N-terminal mutations reduced CAP-CAP multimer formation and SH3 domain binding, although the SH3-binding site is about 350 amino acids away. Finally, disruption of the actin cytoskeleton with latrunculin-A did not affect the cAMP phenotypes of the hyperactive Ras2Val19 allele. These data identify a novel region of CAP that controls access to the SH3-binding site and demonstrate that cytoskeletal localization of CAP or an intact cytoskeleton per se is not necessary for cAMP signaling.

Copyright © 1999 by The American Society for Biochemistry and Molecular Biology, Inc.
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