PEA-15 mediates cytoplasmic sequestration of ERK MAP kinase

被引:267
作者
Formstecher, E
Ramos, JW [1 ]
Fauquet, M
Calderwood, DA
Hsieh, JC
Canton, B
Nguyen, XT
Barnier, JV
Camonis, J
Ginsberg, MH
Chneiweiss, H
机构
[1] Coll France, INSERM, U114, F-75231 Paris 05, France
[2] Scripps Res Inst, Dept Vasc Biol, La Jolla, CA 92037 USA
[3] Inst Curie, Sect Rech, INSERM, U528, F-75248 Paris 05, France
[4] Inst Alfred Fessard, CNRS, UPR 2212, F-91198 Gif Sur Yvette, France
关键词
D O I
10.1016/S1534-5807(01)00035-1
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The ERK 1/2 MAP kinase pathway controls cell growth and survival and modulates integrin function. Here, we report that PEA-15, a protein variably expressed in multiple cell types, blocks ERK-dependent transcription and proliferation by binding ERKs and preventing their localization in the nucleus. PEA-15 contains a nuclear export sequence required for its capacity to anchor ERK in the cytoplasm. Genetic deletion of PEA-15 results in increased ERK nuclear localization with consequent increased cFos transcription and cell proliferation. Thus, PEA-15 can redirect the biological outcome of MAP kinase signaling by regulating the subcellular localization of ERK MAP kinase.
引用
收藏
页码:239 / 250
页数:12
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