| Literature DB >> 9743501 |
H Y Chang1, H Nishitoh, X Yang, H Ichijo, D Baltimore.
Abstract
The Fas death receptor can activate the Jun NH2-terminal kinase (JNK) pathway through the receptor-associated protein Daxx. Daxx was found to activate the JNK kinase kinase ASK1, and overexpression of a kinase-deficient ASK1 mutant inhibited Fas- and Daxx-induced apoptosis and JNK activation. Fas activation induced Daxx to interact with ASK1, which consequently relieved an inhibitory intramolecular interaction between the amino- and carboxyl-termini of ASK1, activating its kinase activity. The Daxx-ASK1 connection completes a signaling pathway from a cell surface death receptor to kinase cascades that modulate nuclear transcription factors.Entities:
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Year: 1998 PMID: 9743501 DOI: 10.1126/science.281.5384.1860
Source DB: PubMed Journal: Science ISSN: 0036-8075 Impact factor: 47.728