Kinase Suppressor of Ras (KSR) Is a Scaffold Which Facilitates Mitogen-Activated Protein Kinase Activation In Vivo

Author:

Nguyen AnhCo1,Burack W. Richard1,Stock Jeffrey L.2,Kortum Robert3,Chaika Oleg V.3,Afkarian Maryam4,Muller William J.5,Murphy Kenneth M.4,Morrison Deborah K.6,Lewis Robert E.3,McNeish John2,Shaw Andrey S.1

Affiliation:

1. Department of Pathology and Immunology

2. Department of Exploratory Medicinal Sciences, Central Research, Pfizer, Inc., Groton, Connecticut 06340

3. Eppley Institute for Research in Cancer and Allied Diseases, Department of Biochemistry and Molecular Biology, Omaha, Nebraska 68198

4. Department of Pathology and Immunology, Howard Hughes Medical Institute, Washington University School of Medicine, St. Louis, Missouri 63110

5. Institute for Molecular Biology and Biotechnology, Department of Biology, McMaster University, Hamilton, Ontario L8S 4K1, Canada

6. Regulation of Cell Growth Laboratory, National Cancer Institute, Frederick Cancer Research and Development Center, Frederick, Maryland 21702

Abstract

ABSTRACT While scaffold proteins are thought to be key components of signaling pathways, their exact function is unknown. By preassembling multiple components of signaling cascades, scaffolds are predicted to influence the efficiency and/or specificity of signaling events. Here we analyze a potential scaffold of the Ras/mitogen-activated protein kinase (MAPK) pathway, kinase suppressor of Ras (KSR), by generating KSR-deficient mice. KSR-deficient mice were grossly normal even though ERK kinase activation was attenuated to a degree sufficient to block T-cell activation and inhibit tumor development. Consistent with its role as a scaffold, high-molecular-weight complexes containing KSR, MEK, and ERK were lost in the absence of KSR. This demonstrates that KSR is a bona fide scaffold that is not required for but enhances signaling via the Ras/MAPK signaling pathway.

Publisher

American Society for Microbiology

Subject

Cell Biology,Molecular Biology

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