Dual engagement of 14-3-3 proteins controls signal relay from ASK2 to the ASK1 signalosome

作者：Cockrell L M; Puckett M C; Goldman E H; Khuri F R; Fu H^*

来源：Oncogene, 2010, 29(6): 822-830.

DOI：10.1038/onc.2009.382

• ASK1
• ASK2
• 14-3-3
• apoptosis
• mitogen-activated protein kinase

Faithful and efficient transmission of biological signals through mitogen-activated protein kinase (MAPK) pathways requires engagement of highly regulated cellular machinery in response to diverse environmental cues. Here, we report a novel mechanism controlling signal relay between two MAP3Ks, apoptosis signal-regulating kinase (ASK) 1 and ASK2. We show that ASK2 specifically interacts with 14-3-3 proteins through phosphorylated S964. Although a 14-3-3-binding defective mutant of ASK1 (S967A) has no effect on the ASK2/14-3-3 interaction, both overexpression of the analogous ASK2 (S964A) mutant and knockdown of ASK2 dramatically reduced the amount of ASK1 complexed with 14-3-3. These data suggest a dominant role of ASK2 in 14-3-3 control of ASK1 function. Indeed, ASK2 S964A-induced dissociation of 14-3-3 from ASK1 correlated with enhanced phosphorylation of ASK1 at T838 and increased c-Jun N-terminal kinase phosphorylation, the two biological readouts of ASK1 activation. Our results suggest a model in which upstream signals couple ASK2 S964 phosphorylation to the ASK1 signalosome through dual engagement of 14-3-3. Oncogene (2010) 29, 822-830; doi:10.1038/onc.2009.382; published online 23 November 2009

• 出版日期2010-2-11