Lopez-Bergami Pablo, Ronai Ze'ev
Signal Transduction Program, The Burnham Institute for Medical Research, 10901 N. Torrey Pines Road, La Jolla, CA 92037, USA.
Int J Biochem Cell Biol. 2008;40(5):1055-64. doi: 10.1016/j.biocel.2007.11.011. Epub 2007 Dec 3.
The c-Jun N-terminal kinases (JNKs) are activated in response to stress, DNA damage, and cytokines by MKK4 and MKK7. We recently demonstrated that PKC can augment the degree of JNK activation by phosphorylating JNK, which requires the adaptor protein RACK1. Here we report on the conditions required for PKC-dependent JNK activation. In vitro kinase assays reveal that PKC phosphorylation of JNK is not sufficient for its activation but rather augments JNK activation by canonical JNK upstream kinases MKK4 or MKK7 alone or in combination. Further, to enhance JNK activity, PKC phosphorylation of JNK should precede its phosphorylation by MKK4/7. Inhibition of PKC phosphorylation of JNK affects both early and late phases of JNK activation following UV-irradiation and reduces the apoptotic response mediated by JNK. These data provide important insight into the requirements for PKC activation of JNK signaling.
c-Jun氨基末端激酶(JNKs)在受到应激、DNA损伤以及细胞因子刺激时,会被MKK4和MKK7激活。我们最近证明,蛋白激酶C(PKC)可通过磷酸化JNK来增强JNK的激活程度,而这需要衔接蛋白RACK1的参与。在此我们报告PKC依赖性JNK激活所需的条件。体外激酶分析表明,PKC对JNK的磷酸化不足以激活JNK,而是单独或联合通过经典的JNK上游激酶MKK4或MKK7增强JNK的激活。此外,为增强JNK活性,PKC对JNK的磷酸化应先于MKK4/7对其的磷酸化。抑制PKC对JNK的磷酸化会影响紫外线照射后JNK激活的早期和晚期阶段,并减少由JNK介导的凋亡反应。这些数据为PKC激活JNK信号通路的要求提供了重要见解。