The functional interaction of 14-3-3 proteins with the ERK1/2 scaffold KSR1 occurs in an isoform-specific manner

Abstract

Identifying 14-3-3 isoform-specific substrates and functions may be of broad relevance to cell signaling research because of the key role played by this family of proteins in many vital processes. A multitude of ligands have been identified, but the extent to which they are isoform-specific is a matter of debate. Herein we demonstrate, both in vitro and in vivo, a specific, functionally relevant interaction of human 14-3-3γ with the molecular scaffold KSR1, which is mediated by the C-terminal stretch of 14-3-3γ. Specific binding to 14-3-3γ protected KSR1 from epidermal growth factor-induced dephosphorylation and impaired its ability to activate ERK2 and facilitate Ras signaling in Xenopus oocytes. Furthermore, RNA interference-mediated inhibition of 14-3-3́ resulted in the accumulation of KSR1 in the plasma membrane, all in accordance with 14-3-3́ being the cytosolic anchor that keeps KSR1 inactive. We also provide evidence that KSR1-bound 14-3-3́ heterodimerized preferentially with selected isoforms and that KSR1 bound monomeric 14-3-3́. In sum, we have demonstrated ligand discrimination among 14-3-3 isoforms and shed light on molecular mechanisms of 14-3-3 functional specificity and KSR1 regulation. © 2008 by The American Society for Biochemistry and Molecular Biology, Inc.