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

Eri Oda(The University of Tokyo), Rieko Ohki(The University of Tokyo), Hideki Murasawa(The University of Tokyo), Jiro Nemoto(The University of Tokyo), Tsukasa Shibue(The University of Tokyo), Toshiharu Yamashita(Sapporo Medical University), Takashi Tokino(Sapporo Medical University), Tadatsugu Taniguchi(The University of Tokyo), Nobuyuki Tanaka(The University of Tokyo)
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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.


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