Published August 28, 1998 | Version public
Journal Article

Essential Role of CED-4 Oligomerization in CED-3 Activation and Apoptosis

Abstract

Control of the activation of apoptosis is important both in development and in protection against cancer. In the classic genetic model Caenorhabditis elegans, the pro-apoptotic protein CED-4 activates the CED-3 caspase and is inhibited by the Bcl-2–like protein CED-9. Both processes are mediated by protein-protein interaction. Facilitating the proximity of CED-3 zymogen molecules was found to induce caspase activation and cell death. CED-4 protein oligomerized in cells and in vitro. This oligomerization induced CED-3 proximity and competed with CED-4:CED-9 interaction. Mutations that abolished CED-4 oligomerization inactivated its ability to activate CED-3. Thus, the mechanism of control is that CED-3 in CED-3:CED-4 complexes is activated by CED-4 oligomerization, which is inhibited by binding of CED-9 to CED-4.

Additional Information

© 1998 American Association for the Advancement of Science. Received 3 June 1998; accepted 13 July 1998. We thank F. Chen and H. R. Horvitz for reagents and discussions, P. Svec and A. Darbinian for technical support, and V. M. Dixit, M. Gilman, S. L. Schreiber, and X. Wang for reagents. Supported by the Leukemia Society of America (to X.Y.), the Medical Scientist Training Program (to H.Y.C.), and NIH grant CA51462.

Additional details

Identifiers

Eprint ID
52093
Resolver ID
CaltechAUTHORS:20141124-102100187

Funding

Leukemia Society of America
NIH
CA51462

Dates

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2014-11-24
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2021-11-10
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