Induction of Apoptosis by ASK1, a Mammalian MAPKKK That Activates SAPK/JNK and p38 Signaling Pathways

Author:

Ichijo Hidenori1,Nishida Eisuke2,Irie Kenji3,Dijke Peter ten4,Saitoh Masao1,Moriguchi Tetsuo2,Takagi Minoru5,Matsumoto Kunihiro3,Miyazono Kohei1,Gotoh Yukiko2

Affiliation:

1. H. Ichijo, M. Saitoh, K. Miyazono, Department of Biochemistry, The Cancer Institute, Tokyo, Japanese Foundation for Cancer Research, 1-37-1 Kami-Ikebukuro, Toshima-ku, Tokyo 170, Japan.

2. E. Nishida, T. Moriguchi, Y. Gotoh, Department of Genetics and Molecular Biology, Institute for Virus Research, Kyoto University, Sakyo-ku, Kyoto 606-01, Japan.

3. K. Irie and K. Matsumoto, Department of Molecular Biology, Faculty of Science, Nagoya University, Chikusa-ku, Nagoya 464-01, Japan.

4. P. ten Dijke, Ludwig Institute for Cancer Research, Box 595, Biomedical Center, S-751 24, Uppsala, Sweden.

5. M. Takagi, Department of Oral Pathology, Tokyo Medical and Dental University, 1-5-45 Yushima, Bunkyo-ku, Tokyo 113, Japan.

Abstract

Mitogen-activated protein (MAP) kinase cascades are activated in response to various extracellular stimuli, including growth factors and environmental stresses. A MAP kinase kinase kinase (MAPKKK), termed ASK1, was identified that activated two different subgroups of MAP kinase kinases (MAPKK), SEK1 (or MKK4) and MKK3/MAPKK6 (or MKK6), which in turn activated stress-activated protein kinase (SAPK, also known as JNK; c-Jun amino-terminal kinase) and p38 subgroups of MAP kinases, respectively. Overexpression of ASK1 induced apoptotic cell death, and ASK1 was activated in cells treated with tumor necrosis factor-α (TNF-α). Moreover, TNF-α-induced apoptosis was inhibited by a catalytically inactive form of ASK1. ASK1 may be a key element in the mechanism of stress- and cytokine-induced apoptosis.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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