BID, BIM, and PUMA are essential for activation of the BAX- and BAK-dependent cell death program

Decheng Ren, Ho Chou Tu, Hyungjin Kim, Gary X. Wang, Gregory R. Bean, Osamu Takeuchi, John R. Jeffers, Gerard P. Zambetti, James J.D. Hsieh, Emily H.Y. Cheng

Research output: Contribution to journalArticlepeer-review

358 Scopus citations

Abstract

Although the proteins BAX and BAK are required for initiation of apoptosis at the mitochondria, how BAX and BAK are activated remains unsettled. We provide in vivo evidence demonstrating an essential role of the proteins BID, BIM, and PUMA in activating BAX and BAK. Bid, Bim, and Puma triple-knockout mice showed the same developmental defects that are associated with deficiency of Bax and Bak, including persistent interdigital webs and imperforate vaginas. Genetic deletion of Bid, Bim, and Puma prevented the homo-oligomerization of BAX and BAK, and thereby cytochrome c-mediated activation of caspases in response to diverse death signals in neurons and T lymphocytes, despite the presence of other BH3-only molecules. Thus, many forms of apoptosis require direct activation of BAX and BAK at the mitochondria by a member of the BID, BIM, or PUMA family of proteins.

Original languageEnglish
Pages (from-to)1390-1393
Number of pages4
JournalScience
Volume330
Issue number6009
DOIs
StatePublished - Dec 3 2010

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