The BioGRID | PUBLICATION VIEW

	Science Jan (1999); 283(5401):543-6
Prevention of constitutive TNF receptor 1 signaling by silencer of death domains.
Jiang Y, Woronicz JD, Liu W, Goeddel DV
Tularik, Two Corporate Drive, South San Francisco, CA 94080, USA.
Abstract: Tumor necrosis factor receptor type 1 (TNF-R1) contains a cytoplasmic death domain that is required for the signaling of TNF activities such as apoptosis and nuclear factor kappa B (NF-kappaB) activation. Normally, these signals are generated only after TNF-induced receptor aggregation. However, TNF-R1 self-associates and signals independently of ligand when overexpressed. This apparent paradox may be explained by silencer of death domains (SODD), a widely expressed approximately 60-kilodalton protein that was found to be associated with the death domain of TNF-R1. TNF treatment released SODD from TNF-R1, permitting the recruitment of proteins such as TRADD and TRAF2 to the active TNF-R1 signaling complex. SODD also interacted with death receptor-3 (DR3), another member of the TNF receptor superfamily. Thus, SODD association may be representative of a general mechanism for preventing spontaneous signaling by death domain-containing receptors.
[PUBMED: 9915703]