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


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.

SUBMITTER: Ren D 

PROVIDER: S-EPMC3163443 | biostudies-literature | 2010 Dec

REPOSITORIES: biostudies-literature

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

Ren Decheng D   Tu Ho-Chou HC   Kim Hyungjin H   Wang Gary X GX   Bean Gregory R GR   Takeuchi Osamu O   Jeffers John R JR   Zambetti Gerard P GP   Hsieh James J-D JJ   Cheng Emily H-Y EH  

Science (New York, N.Y.) 20101201 6009


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  ...[more]

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