Morley S J, McKendrick L
Biochemistry Laboratory, School of Biological Sciences, University of Sussex, Falmer, Brighton BN1 9QG, United Kingdom.
J Biol Chem. 1997 Jul 11;272(28):17887-93. doi: 10.1074/jbc.272.28.17887.
The initiation factor (eIF) 4E is regulated by modulating both the phosphorylation and the availability of the protein to participate in the initiation process. Here we show that either serum treatment or activation of the stress-activated protein kinase (JNK/SAPK) led to enhanced phosphorylation of eIF4E in quiescent NIH 3T3 cells. Although the immunosuppressant, rapamycin, was found to stabilize the association of eIF4E with its negative regulator, 4E-BP1, this drug did not prevent the early effects of serum stimulation on the overall rate of translation, polysome formation, the phosphorylation status of eIF4E, or the recruitment of eIF4E into the eIF4F complex. However, the rapid enhancement of eIF4E phosphorylation in response to serum was largely prevented by the inhibitor of mitogen-activated protein (MAP) kinase activation, PD98059. Activation of the JNK/SAPK signaling pathway with anisomycin resulted in enhanced phosphorylation of eIF4E, which was prevented by either rapamycin or the highly specific p38 MAP kinase inhibitor, SB203580. These data illustrate that multiple signaling pathways, including those of distinct members of the MAP kinase family, mediate the phosphorylation of eIF4E and that the association of eIF4E with 4E-BP1 does not necessarily prevent phosphorylation of eIF4E in vivo.
起始因子(eIF)4E通过调节磷酸化以及该蛋白参与起始过程的可用性来进行调控。在此我们表明,血清处理或应激激活蛋白激酶(JNK/SAPK)的激活均会导致静止的NIH 3T3细胞中eIF4E磷酸化增强。尽管发现免疫抑制剂雷帕霉素可稳定eIF4E与其负调节因子4E-BP1的结合,但该药物并不能阻止血清刺激对整体翻译速率、多核糖体形成、eIF4E的磷酸化状态或eIF4E募集到eIF4F复合物中的早期影响。然而,丝裂原活化蛋白(MAP)激酶激活抑制剂PD98059在很大程度上阻止了血清刺激引起的eIF4E磷酸化的快速增强。茴香霉素激活JNK/SAPK信号通路导致eIF4E磷酸化增强,而雷帕霉素或高度特异性的p38 MAP激酶抑制剂SB203580均可阻止这种增强。这些数据表明,包括MAP激酶家族不同成员的信号通路在内的多种信号通路介导了eIF4E的磷酸化,并且eIF4E与4E-BP1的结合并不一定能在体内阻止eIF4E的磷酸化。