FADD: Essential for Embryo Development and Signaling from Some, But Not All, Inducers of Apoptosis

Author:

Yeh Wen-Chen1234,Pompa José Luis de la1234,McCurrach Mila E.1234,Shu Hong-Bing1234,Elia Andrew J.1234,Shahinian Arda1234,Ng Michelle1234,Wakeham Andrew1234,Khoo Wilson1234,Mitchell Kyran1234,El-Deiry Wafik S.1234,Lowe Scott W.1234,Goeddel David V.1234,Mak Tak W.1234

Affiliation:

1. W.-C. Yeh, J. L. de la Pompa, A. J. Elia, A. Shahinian, M. Ng, A. Wakeham, W. Khoo, T. W. Mak, Amgen Institute, Departments of Medical Biophysics and Immunology, University of Toronto, and Ontario Cancer Institute, 610 University Avenue, Toronto, Ontario M5G 2C1, Canada.

2. M. E. McCurrach and S. W. Lowe, Cold Spring Harbor Laboratories, 1 Bungtown Road, Cold Spring Harbor, NY 11724, USA.

3. H.-B. Shu and D. V. Goeddel, Tularik, 2 Corporate Drive, South San Francisco, CA 94080, USA.

4. K. Mitchell and W. S. El-Deiry, Howard Hughes Medical Institute, University of Pennsylvania School of Medicine CRB 437A, Philadelphia, PA 19104, USA.

Abstract

FADD (also known as Mort-1) is a signal transducer downstream of cell death receptor CD95 (also called Fas). CD95, tumor necrosis factor receptor type 1 (TNFR-1), and death receptor 3 (DR3) did not induce apoptosis in FADD-deficient embryonic fibroblasts, whereas DR4, oncogenes E1A and c- myc , and chemotherapeutic agent adriamycin did. Mice with a deletion in the FADD gene did not survive beyond day 11.5 of embryogenesis; these mice showed signs of cardiac failure and abdominal hemorrhage. Chimeric embryos showing a high contribution of FADD null mutant cells to the heart reproduce the phenotype of FADD-deficient mutants. Thus, not only death receptors, but also receptors that couple to developmental programs, may use FADD for signaling.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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