Induction of apoptosis by the Bcl-2 homologue Bak (original) (raw)
- Letter
- Published: 20 April 1995
- Elizabeth A. Harrington1 na1,
- Rosemary O'Connor1,
- Cathy Remington1,
- Robert J. Lutz1,
- Gerard I. Evan1 na1 &
- …
- Braydon C. Guild1
Nature volume 374, pages 733–736 (1995)Cite this article
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Abstract
CELLS are eliminated in a variety of physiological settings by apoptosis, a genetically encoded process of cellular suicide1,2. Apoptosis comprises an intrinsic cellular defence against tumorigenesis, which, when suppressed, may contribute to the development of malignancies3. The _bcl_-2oncogene, which is activated in follicular lymphomas, functions as a potent suppressor of apoptosis under diverse conditions4. Here we describe the complementary DNA cloning and functional analysis of a new Bcl-2 homologue, Bak, which promotes cell death and counteracts the protection from apoptosis provided by Bcl-2. Moreover, enforced expression of Bak induces rapid and extensive apoptosis of serum-deprived fibroblasts. This raises the possibility that Bak is directly involved in activating the cell death machinery.
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Author notes
- Elizabeth A. Harrington and Gerard I. Evan: Imperial Cancer Research Fund Laboratories, 44 Lincoln's Inn Fields, London WC2A 3PX, UK
Authors and Affiliations
- Apoptosis Technology Inc., 148 Sidney Street, Cambridge, Massachusetts, 02139, USA
Thomas Chittenden, Elizabeth A. Harrington, Rosemary O'Connor, Cathy Remington, Robert J. Lutz, Gerard I. Evan & Braydon C. Guild
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- Thomas Chittenden
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Chittenden, T., Harrington, E., O'Connor, R. et al. Induction of apoptosis by the Bcl-2 homologue Bak.Nature 374, 733–736 (1995). https://doi.org/10.1038/374733a0
- Received: 26 October 1994
- Accepted: 02 March 1995
- Issue Date: 20 April 1995
- DOI: https://doi.org/10.1038/374733a0