1. Academic Validation
  2. A novel receptor for Apo2L/TRAIL contains a truncated death domain

A novel receptor for Apo2L/TRAIL contains a truncated death domain

  • Curr Biol. 1997 Dec 1;7(12):1003-6. doi: 10.1016/s0960-9822(06)00422-2.
S A Marsters 1 J P Sheridan R M Pitti A Huang M Skubatch D Baldwin J Yuan A Gurney A D Goddard P Godowski A Ashkenazi
Affiliations

Affiliation

  • 1 Department of Molecular Oncology, Genentech Inc., 1 DNA Way, South San Francisco, California 94080-4918, USA.
Abstract

Apo2 ligand (Apo2L [1], also called TRAIL for tumor necrosis factor (TNF)-related apoptosis-inducing ligand [2]) belongs to the TNF family and activates Apoptosis in tumor cells. Three closely related receptors bind Apo2L: DR4 and DR5, which contain cytoplasmic death domains and signal Apoptosis, and DcR1, a decoy receptor that lacks a cytoplasmic tail and inhibits Apo2L function [3-5]. By cross-hybridization with DcR1, we have identified a fourth Apo2L receptor, which contains a cytoplasmic region with a truncated death domain. We subsequently named this protein Decoy Receptor 2 (DcR2). The DcR2 gene mapped to human chromosome 8p21, as did the genes encoding DR4, DR5 and DcR1. A single DcR2 mRNA transcript showed a unique expression pattern in human tissues and was particularly abundant in fetal liver and adult testis. Upon overexpression, DcR2 did not activate Apoptosis or nuclear factor-kappaB; however, it substantially reduced cellular sensitivity to Apo2L-induced Apoptosis. These results suggest that DcR2 functions as an inhibitory Apo2L receptor.

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