ASK1
死亡相关蛋白6
细胞周期蛋白依赖激酶9
MAP激酶激酶激酶
细胞生物学
丝裂原活化蛋白激酶激酶
地图2K7
激酶
蛋白激酶R
c-Raf公司
癌症研究
信号转导
细胞周期蛋白依赖激酶2
蛋白激酶A
化学
生物
转录因子
生物化学
核蛋白
基因
作者
Howard Y. Chang,Hideki Nishitoh,Xiaolu Yang,Hidenori Ichijo,David Baltimore
出处
期刊:Science
[American Association for the Advancement of Science (AAAS)]
日期:1998-09-18
卷期号:281 (5384): 1860-1863
被引量:596
标识
DOI:10.1126/science.281.5384.1860
摘要
The Fas death receptor can activate the Jun NH 2 -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.
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