Protection against Fas/APO-1- and tumor necrosis factor-mediated cell death by a novel protein, sentrin

Fas/APO-1 and TNF receptor 1 share a common signaling motif in their cytoplasmic tail called the "death domain." Using the death domain as bait in the yeast two-hybrid system, several death domain-containing proteins that participate in cell death signaling have been identified. Here we re...

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Veröffentlicht in:The Journal of immunology (1950) 1996-11, Vol.157 (10), p.4277-4281
Hauptverfasser: Okura, T, Gong, L, Kamitani, T, Wada, T, Okura, I, Wei, CF, Chang, HM, Yeh, ET
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Sprache:eng
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Zusammenfassung:Fas/APO-1 and TNF receptor 1 share a common signaling motif in their cytoplasmic tail called the "death domain." Using the death domain as bait in the yeast two-hybrid system, several death domain-containing proteins that participate in cell death signaling have been identified. Here we report the isolation of a novel protein, sentrin, which interacts with Fas/APO-1 and TNF receptor 1 but not with FADD/MORT1 or CD40. Two-hybrid interaction assays reveal that sentrin associates only with the signal-competent forms of Fas/APO-1 or TNF receptor 1 death domains. Sentrin is a novel protein of 101 amino acids with homology to ubiquitin, Nedd8, and a Saccharomyces cerevisiae protein, Smt3. When overexpressed, sentrin provides protection against both anti-Fas/APO-1 and TNF-induced cell death.
ISSN:0022-1767
1550-6606
DOI:10.4049/jimmunol.157.10.4277