Activation of Apoptosis Signal-Regulating Kinase 1 (ASK1) by the Adapter Protein Daxx

Author:

Chang Howard Y.1,Nishitoh Hideki1,Yang Xiaolu1,Ichijo Hidenori1,Baltimore David1

Affiliation:

1. H. Y. Chang and X. Yang, Department of Biology, Massachusetts Institute of Technology, Cambridge, MA 02138, USA. H. Nishitoh and H. Ichijo, Department of Biomaterials Science, Faculty of Dentistry, Tokyo Medical and Dental University, 1-5-45 Yushima, Bunkyo-ku, Tokyo 113-8549, and Department of Biochemistry, Cancer Institute, Tokyo, Japanese Foundation for Cancer Research, 1-37-1 Kami-Ikebukuro, Toshima-ku, Tokyo 170, Japan. D. Baltimore, Department of Biology, Massachusetts Institute of Technology,...

Abstract

The Fas death receptor can activate the Jun NH 2 -terminal kinase (JNK) pathway through the receptor-associated protein Daxx. Daxx was found to activate the JNK kinase kinase ASK1, and overexpression of a kinase-deficient ASK1 mutant inhibited Fas- and Daxx-induced apoptosis and JNK activation. Fas activation induced Daxx to interact with ASK1, which consequently relieved an inhibitory intramolecular interaction between the amino- and carboxyl-termini of ASK1, activating its kinase activity. The Daxx-ASK1 connection completes a signaling pathway from a cell surface death receptor to kinase cascades that modulate nuclear transcription factors.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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