Noxa, a BH3-Only Member of the Bcl-2 Family and Candidate Mediator of p53-Induced Apoptosis

Author:

Oda Eri1,Ohki Rieko1,Murasawa Hideki1,Nemoto Jiro1,Shibue Tsukasa1,Yamashita Toshiharu2,Tokino Takashi2,Taniguchi Tadatsugu1,Tanaka † Nobuyuki1

Affiliation:

1. Department of Immunology, Graduate School of Medicine and Faculty of Medicine, University of Tokyo, Hongo 7-3-1, Bunkyo-ku, Tokyo 113-0033, Japan.

2. Department of Molecular Biology, Cancer Research Institute, Sapporo Medical University School of Medicine, S1 W17, Chuo-Ku, Sapporo 060-8543, Japan.

Abstract

A critical function of tumor suppressor p53 is the induction of apoptosis in cells exposed to noxious stresses. We report a previously unidentified pro-apoptotic gene, Noxa . Expression of Noxa induction in primary mouse cells exposed to x-ray irradiation was dependent on p53. Noxa encodes a Bcl-2 homology 3 (BH3)–only member of the Bcl-2 family of proteins; this member contains the BH3 region but not other BH domains. When ectopically expressed, Noxa underwent BH3 motif–dependent localization to mitochondria and interacted with anti-apoptotic Bcl-2 family members, resulting in the activation of caspase-9. We also demonstrate that blocking the endogenous Noxa induction results in the suppression of apoptosis. Noxa may thus represent a mediator of p53-dependent apoptosis.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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