Activation of MEK kinase 1 by the c-Abl protein tyrosine kinase in response to DNA damage

被引:76
作者
Kharbanda, S
Pandey, P
Yamauchi, T
Kumar, S
Kaneki, M
Kumar, V
Bharti, A
Yuan, ZM
Ghanem, L
Rana, A
Weichselbaum, R
Johnson, G
Kufe, D
机构
[1] Harvard Univ, Sch Med, Dana Farber Canc Inst, Boston, MA 02115 USA
[2] Harvard Univ, Sch Med, Massachusetts Gen Hosp, Dept Mol Biol,Diabet Res Lab, Boston, MA 02114 USA
[3] Univ Chicago, Dept Radiat & Cellular Oncol, Chicago, IL 60637 USA
[4] Natl Jewish Ctr Immunol & Resp Med, Div Basic Sci, Denver, CO 80262 USA
关键词
D O I
10.1128/MCB.20.14.4979-4989.2000
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
The c-Abl protein tyrosine kinase is activated by certain DNA-damaging agents and regulates induction of the stress-activated c-Jun N-terminal protein kinase (SAPK). Here we show that nuclear c-Abl associates with MEK kinase 1 (MEKK-1), an upstream effector of the SEK1-->SAPK pathway, in the response of cells to genotoxic stress. The results demonstrate that the nuclear c-Abl binds to MEKK-1 and that c-Abl phosphorylates MEKK-1 in vitro and in vivo. Transient-transfection studies with wild-type and kinase-inactive c-Abl demonstrate c-Abl kinase-dependent activation of MEKK-1. Moreover, c-Abl activates MEKK-1 in vitro and in response to DNA damage. The results also demonstrate that c-AbI induces MEKK-1-mediated phosphorylation and activation of SEK1-SAPK in coupled kinase assays. These findings indicate that c-Abl functions upstream of MEKK-1-dependent activation of SAPK in the response to genotoxic stress.
引用
收藏
页码:4979 / 4989
页数:11
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