Human CNK1 acts as a scaffold protein, linking Rho and Ras signal transduction pathways

• Rho family GTPases act as molecular switches to control a variety of cellular responses, including cytoskeletal rearrangements, changes in gene expression, and cell transformation. In the active, GTP-bound state, Rho interacts with an ever-growing number of effector molecules, which promote distinct biochemical pathways. Here, we describe the isolation of hCNK1, the human homologue of Drosophila connector enhancer of ksr, as an effector for Rho. hCNK1 contains several protein-protein interaction domains, and Rho interacts with one of these, the PH domain, in a GTP-dependent manner. A mutant hCNK1, which is unable to bind to Rho, or depletion of endogenous hCNK1 by using RNA interference inhibits Rho-induced gene expression via serum response factor but has no apparent effect on Rho-induced stress fiber formation, suggesting that it acts as a specific effector for transcriptional, but not cytoskeletal, activation pathways. Finally, hCNK1 associates with Rhophilin and RalGDS, Rho and Ras effector molecules, respectively, suggesting that it acts as a scaffold protein to mediate cross talk between the two pathways.

Nyckelord

Adaptor Proteins; Signal Transducing

Animals

COS Cells

Carrier Proteins/chemistry/genetics/*metabolism

Drosophila Proteins

Hela Cells

Humans

Mutation; Missense

Oncogene Protein p21(ras)/*metabolism

Protein Binding

Protein Structure; Tertiary

Protein-Serine-Threonine Kinases/metabolism

Research Support; Non-U.S. Gov't

Sequence Deletion

Serum Response Factor/metabolism

Signal Transduction

Stress Fibers/metabolism

Transcription; Genetic

ral Guanine Nucleotide Exchange Factor/metabolism

rho GTP-Binding Proteins/*metabolism

rhoA GTP-Binding Protein/metabolism

Publikations- och innehållstyp

ref (ämneskategori)

art (ämneskategori)