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A Novel Protein That Interacts with the Death Domain of Fas/APO1 Contains a Sequence Motif Related to the Death Domain
- Source :
- Journal of Biological Chemistry. 270:7795-7798
- Publication Year :
- 1995
- Publisher :
- Elsevier BV, 1995.
-
Abstract
- Signaling for cell death by Fas/APO1 occurs via a distinct region in its intracellular domain. This region contains a conserved sequence motif, the death domain motif, that is also found in the intracellular domains of the p55 tumor necrosis factor receptor and the low affinity nerve growth factor receptor, as well as in the regulatory domain of the ankyrins. A novel protein that specifically binds to the death domain of Fas/APO1 but not to Fas/APO1 molecules with a loss of function point mutation occurring in lprcg mice was cloned by a two-hybrid screen of a HeLa cells' cDNA library. The cloned protein itself contains a death domain motif, and this region binds to the death domain of Fas/APO1, while the region upstream to the death domain prompts self-association of the protein. Induced expression of the protein results in ligand-independent triggering of cytotoxicity, suggesting that it is involved in cell death induction by Fas/APO1.
- Subjects :
- DNA, Complementary
Fas-Associated Death Domain Protein
Molecular Sequence Data
Apoptosis
Biochemistry
Pyrin domain
Mice
EVH1 domain
Animals
Humans
Amino Acid Sequence
fas Receptor
FADD
Cloning, Molecular
Molecular Biology
Adaptor Proteins, Signal Transducing
Death domain
Sequence Homology, Amino Acid
biology
Proteins
Cell Biology
Fas receptor
Molecular biology
Antigens, Surface
biology.protein
Fas signaling pathway
Death effector domain
GRB2
Carrier Proteins
HeLa Cells
Subjects
Details
- ISSN :
- 00219258
- Volume :
- 270
- Database :
- OpenAIRE
- Journal :
- Journal of Biological Chemistry
- Accession number :
- edsair.doi.dedup.....f96924bcaaf76d649104bf733e3b0fe5