Chemical genetic analysis of the time course of signal transduction by JNK

被引:275
作者
Ventura, JJ
Hübner, A
Zhang, C
Flavel, RA
Shokat, KM
Davis, RJ [1 ]
机构
[1] Univ Massachusetts, Sch Med, Howard Hughes Med Inst, Worcester, MA 01605 USA
[2] Univ Massachusetts, Sch Med, Program Mol Med, Worcester, MA 01605 USA
[3] Univ Calif San Francisco, Howard Hughes Med Inst, San Francisco, CA 94143 USA
[4] Univ Calif San Francisco, Dept Mol & Cellular Pharmacol, San Francisco, CA 94143 USA
[5] Yale Univ, Sch Med, Howard Hughes Med Inst, New Haven, CT 06520 USA
[6] Yale Univ, Sch Med, Immunobiol Sect, New Haven, CT 06520 USA
基金
英国医学研究理事会;
关键词
D O I
10.1016/j.molcel.2006.01.018
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Exposure of primary murine embryonic fibroblasts to tumor necrosis factor (TNF) causes biphasic activation of the c-Jun NH2-terminal kinase (JNK) signaling pathway. The early phase (30 min) of the response to TNF is a large and transient increase in JNK activity. This response is followed by a second and more sustained phase of JNK activation that lasts many hours. We employed a chemical genetic strategy to dissect the functional consequences of these two phases of JNK activation. We report that both the early and late phases of JNK activation contribute to TNF-incluced gene expression. In contrast, the early transient phase of JNK activation (< 1 hr) can signal cell survival, while the later and more sustained phase of JNK activation (1-6 hr) can mediate proapoptotic signaling. These data indicate that the time course of JNK signaling can influence the biological response to JNK activation.
引用
收藏
页码:701 / 710
页数:10
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