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

被引:278
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
相关论文
共 70 条
[1]   Characterization of the c-Jun N-terminal kinase-BimEL signaling pathway in neuronal apoptosis [J].
Becker, EBE ;
Howell, J ;
Kodama, Y ;
Barker, PA ;
Bonni, A .
JOURNAL OF NEUROSCIENCE, 2004, 24 (40) :8762-8770
[2]   Acquisition of inhibitor-sensitive protein kinases through protein design [J].
Bishop, AC ;
Shokat, KM .
PHARMACOLOGY & THERAPEUTICS, 1999, 82 (2-3) :337-346
[3]   A chemical switch for inhibitor-sensitive alleles of any protein kinase [J].
Bishop, AC ;
Ubersax, JA ;
Petsch, DT ;
Matheos, DP ;
Gray, NS ;
Blethrow, J ;
Shimizu, E ;
Tsien, JZ ;
Schultz, PG ;
Rose, MD ;
Wood, JL ;
Morgan, DO ;
Shokat, KM .
NATURE, 2000, 407 (6802) :395-401
[4]   Role of MLK3 in the regulation of mitogen-activated protein kinase signaling cascades [J].
Brancho, D ;
Ventura, JJ ;
Jaeschke, A ;
Doran, B ;
Flavell, RA ;
Davis, RJ .
MOLECULAR AND CELLULAR BIOLOGY, 2005, 25 (09) :3670-3681
[5]   ACTIVATION OF MAP KINASE KINASE IS NECESSARY AND SUFFICIENT FOR PC12 DIFFERENTIATION AND FOR TRANSFORMATION OF NIH 3T3 CELLS [J].
COWLEY, S ;
PATERSON, H ;
KEMP, P ;
MARSHALL, CJ .
CELL, 1994, 77 (06) :841-852
[6]   Tpl2/Cot signals activate ERK, JNK, and NF-κB in a cell-type and stimulus-specific manner [J].
Das, S ;
Cho, J ;
Lambertz, I ;
Kelliher, MA ;
Eliopoulos, AG ;
Du, KY ;
Tsichlis, PN .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2005, 280 (25) :23748-23757
[7]   Signal transduction by the JNK group of MAP kinases [J].
Davis, RJ .
CELL, 2000, 103 (02) :239-252
[8]   Induction of gadd45β by NF-κB downregulates pro-apoptotic JNK signalling [J].
De Smaele, E ;
Zazzeroni, F ;
Papa, S ;
Nguyen, DU ;
Jin, RG ;
Jones, J ;
Cong, R ;
Franzoso, G .
NATURE, 2001, 414 (6861) :308-313
[9]   A JNK-dependent pathway is required for TNFα-induced apoptosis [J].
Deng, YB ;
Ren, XY ;
Yang, L ;
Lin, YH ;
Wu, XW .
CELL, 2003, 115 (01) :61-70
[10]   JNK phosphorylation and activation of BAD couples the stress-activated signaling pathway to the cell death machinery [J].
Donovan, N ;
Becker, EBE ;
Konishi, Y ;
Bonni, A .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (43) :40944-40949