Bouchard Caroline, Marquardt Judith, Brás Alexandra, Medema René H, Eilers Martin
Institute for Molecular Biology and Tumor Research, Marburg, Germany.
EMBO J. 2004 Jul 21;23(14):2830-40. doi: 10.1038/sj.emboj.7600279. Epub 2004 Jul 8.
Myc synergizes with Ras and PI3-kinase in cell transformation, yet the molecular basis for this behavior is poorly understood. We now show that Myc recruits TFIIH, P-TEFb and Mediator to the cyclin D2 and other target promoters, while the PI3-kinase pathway controls formation of the pre-initiation complex and loading of RNA polymerase II. The PI3-kinase pathway involves Akt-mediated phosphorylation of FoxO transcription factors. In a nonphosphorylated state, FoxO factors inhibit induction of multiple Myc target genes, Myc-induced cell proliferation and transformation by Myc and Ras. Abrogation of FoxO function enables Myc to activate target genes in the absence of PI3-kinase activity and to induce foci formation in primary cells in the absence of oncogenic Ras. We suggest that the cooperativity between Myc and Ras is at least in part due to the fact that Myc and FoxO proteins control distinct steps in the activation of an overlapping set of critical target genes.
Myc在细胞转化过程中与Ras和PI3激酶协同作用,但其这种行为的分子基础却知之甚少。我们现在发现,Myc可将TFIIH、P-TEFb和中介体招募至细胞周期蛋白D2及其他靶启动子处,而PI3激酶途径则控制前起始复合物的形成以及RNA聚合酶II的装载。PI3激酶途径涉及Akt介导的FoxO转录因子磷酸化。处于非磷酸化状态时,FoxO因子会抑制多个Myc靶基因的诱导、Myc诱导的细胞增殖以及Myc和Ras介导的细胞转化。FoxO功能的缺失使Myc能够在缺乏PI3激酶活性的情况下激活靶基因,并在缺乏致癌性Ras的情况下诱导原代细胞中的病灶形成。我们认为,Myc与Ras之间的协同作用至少部分归因于Myc和FoxO蛋白控制一组重叠的关键靶基因激活过程中不同步骤这一事实。