A NOVEL KINASE CASCADE TRIGGERED BY STRESS AND HEAT-SHOCK THAT STIMULATES MAPKAP KINASE-2 AND PHOSPHORYLATION OF THE SMALL HEAT-SHOCK PROTEINS

被引:1577
作者
ROUSE, J
COHEN, P
TRIGON, S
MORANGE, M
ALONSOLLAMAZARES, A
ZAMANILLO, D
HUNT, T
NEBREDA, AR
机构
[1] ECOLE NORMALE SUPER, DEPT BIOL, MOLEC GENET UNIT, F-75230 PARIS 05, FRANCE
[2] IMPERIAL CANC RES FUND, CLARE HALL LABS, S MIMMS EN6 3LD, HERTS, ENGLAND
基金
英国医学研究理事会;
关键词
D O I
10.1016/0092-8674(94)90277-1
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
MAPK-activated protein kinase-2 (MAPKAP kinase-2) is activated in vitro by the p42 and p44 isoforms of MAPK (p42/p44(MAPK)). In several cell lines, however, MAPKAP kinase-2 is activated by sodium arsenite, heat shock, or osmotic stress and not by agonists that activate p42/p44(MAPK). We have identified a MAPK-like enzyme that acts as a MAPKAP kinase-a reactivating kinase (RK). RK is recognized by an antiserum raised against a Xenopus MAPK (Mpk2), which is most similar to HOG1 from S. cerevisiae. We also identified a RK kinase (RKK) on the basis of its ability to activate either RK or a GST-Mpk2 fusion protein. The RKK, RK, and MAPKAP kinase-2 constitute a new stress-activated signal transduction pathway in vertebrates that is distinct from the classical MAPK cascade.
引用
收藏
页码:1027 / 1037
页数:11
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