Tiam1 mediates Ras activation of Rac by a PI(3)K-independent mechanism

John M. Lambert, Que T. Lambert, Gary W. Reuther, Angeliki Malliri, David P. Siderovski, John Sondek, John G. Collard, Chaning J. Der

Research output: Contribution to journalArticlepeer-review


Rac is a member of the Ras superfamily of GTPases and functions as a GDP/GTP-regulated switch1. Formation of active Rac-GTP is stimulated by Dbl family guanine nucleotide exchange factors (GEFs), such as Tiam1 (ref. 2). Once activated, Rac stimulates signalling pathways that regulate actin organization, gene expression and cellular proliferation. Rac also functions downstream of the Ras oncoprotein in pathways that stimulate membrane ruffling3, growth transformation4,5, activation of the c-Jun amino-terminal kinase (JNK) mitogen-activated protein kinase6, activation of the NF-κB transcription factor and promotion of cell survival7,8. Although recent studies support phosphatidylinositol 3-OH kinase (PI(3)K)-dependent mechanisms through which Ras might activate Rac (refs 9,10), the precise mechanism remains to be determined. Here we demonstrate that Tiam1, a Rac-specific GEF, preferentially associates with activated GTP-bound Ras through a Ras-binding domain. Furthermore, activated Ras and Tiam1 cooperate to cause synergistic formation of Rac-GTP in a PI(3)K-independent manner. Thus, Tiam1 can function as an effector that directly mediates Ras activation of Rac.
Original languageEnglish
Pages (from-to)621-625
Number of pages4
JournalNature Cell Biology
Issue number8
Publication statusPublished - 2002


  • metabolism: 1-Phosphatidylinositol 3-Kinase
  • 3T3 Cells
  • Animals
  • Binding Sites
  • Cell Line
  • Humans
  • Mice
  • Protein Structure, Tertiary
  • chemistry: Proteins
  • chemistry: Recombinant Proteins
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.
  • metabolism: rac GTP-Binding Proteins
  • metabolism: ras Proteins


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