Formstecher E, Ramos J W, Fauquet M, Calderwood D A, Hsieh J C, Canton B, Nguyen X T, Barnier J V, Camonis J, Ginsberg M H, Chneiweiss H
INSERM U114, Collège de France, Paris.
Dev Cell. 2001 Aug;1(2):239-50. doi: 10.1016/s1534-5807(01)00035-1.
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.
ERK 1/2丝裂原活化蛋白激酶通路控制细胞生长与存活,并调节整合素功能。在此,我们报告称,PEA-15是一种在多种细胞类型中表达各异的蛋白质,它通过结合ERK并阻止其定位于细胞核,从而阻断ERK依赖的转录和增殖。PEA-15含有一个核输出序列,该序列是其将ERK锚定在细胞质中所必需的。PEA-15的基因缺失导致ERK核定位增加,从而导致cFos转录和细胞增殖增加。因此,PEA-15可通过调节ERK丝裂原活化蛋白激酶的亚细胞定位来改变丝裂原活化蛋白激酶信号的生物学结果。