1. Academic Validation
  2. ASK1 is essential for JNK/SAPK activation by TRAF2

ASK1 is essential for JNK/SAPK activation by TRAF2

  • Mol Cell. 1998 Sep;2(3):389-95. doi: 10.1016/s1097-2765(00)80283-x.
H Nishitoh 1 M Saitoh Y Mochida K Takeda H Nakano M Rothe K Miyazono H Ichijo
Affiliations

Affiliation

  • 1 Department of Biochemistry, Cancer Institute, Tokyo, Japan.
Abstract

Tumor necrosis factor (TNF)-induced activation of the c-jun N-terminal kinase (JNK, also known as SAPK; stress-activated protein kinase) requires TNF receptor-associated factor 2 (TRAF2). The Apoptosis signal-regulating kinase 1 (ASK1) is activated by TNF and stimulates JNK activation. Here we show that ASK1 interacts with members of the TRAF family and is activated by TRAF2, TRAF5, and TRAF6 overexpression. A truncated derivative of TRAF2, which inhibits JNK activation by TNF, blocks TNF-induced ASK1 activation. A catalytically inactive mutant of ASK1 is a dominant-negative inhibitor of TNF- and TRAF2-induced JNK activation. In untransfected mammalian cells, ASK1 rapidly associates with TRAF2 in a TNF-dependent manner. Thus, ASK1 is a mediator of TRAF2-induced JNK activation.

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