KSR is a scaffold required for activation of the ERK/MAPK module

  1. François Roy,
  2. Gino Laberge,
  3. Mélanie Douziech,
  4. David Ferland-McCollough, and
  5. Marc Therrien1
  1. Clinical Research Institute of Montreal, Laboratory of Intracellular Signaling, Montreal, PQ Canada H2W 1R7

Abstract

Mechanisms that regulate signal propagation through the ERK/MAPK pathway are still poorly understood. Several proteins are suspected to play critical roles in this process. One of these is Kinase Suppressor of Ras (KSR), a component previously identified in RAS-dependent genetic screens in Drosophila and Caenorhabditis elegans. Here, we show that KSR functions upstream of MEK within the ERK/MAPK module. In agreement with this, we found that KSR facilitates the phosphorylation of MEK by RAF. We further show that KSR associates independently with RAF and MEK, and that these interactions lead to the formation of a RAF/MEK complex, thereby positioning RAF in close proximity to its substrate MEK. These findings suggest that KSR functions as a scaffold that assembles the RAF/MEK functional pair.

Keywords

Footnotes

  • 1 Corresponding author.

  • E-MAIL therrim{at}ircm.qc.ca; FAX (514) 987-5591.

  • Article and publication are at http://www.genesdev.org/cgi/doi/10.1101/gad.962902.

    • Received November 15, 2001.
    • Accepted December 21, 2001.
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