Dhillon Amardeep S, Meikle Sharon, Peyssonnaux Carole, Grindlay Joan, Kaiser Christian, Steen Helge, Shaw Peter E, Mischak Harald, Eychène Alain, Kolch Walter
The Beatson Institute for Cancer Research, CR-UK Beatson Laboratories, Garscube Estate, Bearsden, Glasgow G61 1BD, Scotland, UK.
Mol Cell Biol. 2003 Mar;23(6):1983-93. doi: 10.1128/MCB.23.6.1983-1993.2003.
It is widely thought that the biological outcomes of Raf-1 activation are solely attributable to the activation of the MEK/extracellular signal-regulated kinase (ERK) pathway. However, an increasing number of reports suggest that some Raf-1 functions are independent of this pathway. In this report we show that mutation of the amino-terminal 14-3-3 binding site of Raf-1 uncouples its ability to activate the MEK/ERK pathway from the induction of cell transformation and differentiation. In NIH 3T3 fibroblasts and COS-1 cells, mutation of serine 259 resulted in Raf-1 proteins which activated the MEK/ERK pathway as efficiently as v-Raf. However, in contrast to v-Raf, RafS259 mutants failed to transform. They induced morphological alterations and slightly accelerated proliferation in NIH 3T3 fibroblasts but were not tumorigenic in mice and behaved like wild-type Raf-1 in transformation assays measuring loss of contact inhibition or anchorage-independent growth. Curiously, the RafS259 mutants inhibited focus induction by an activated MEK allele, suggesting that they can hyperactivate negative-feedback pathways. In primary cultures of postmitotic chicken neuroretina cells, RafS259A was able to sustain proliferation to a level comparable to that sustained by the membrane-targeted transforming Raf-1 protein, RafCAAX. In contrast, RafS259A was only a poor inducer of neurite formation in PC12 cells in comparison to RafCAAX. Thus, RafS259 mutants genetically separate MEK/ERK activation from the ability of Raf-1 to induce transformation and differentiation. The results further suggest that RafS259 mutants inhibit signaling pathways required to promote these biological processes.
人们普遍认为,Raf-1激活的生物学结果完全归因于MEK/细胞外信号调节激酶(ERK)途径的激活。然而,越来越多的报道表明,Raf-1的某些功能独立于该途径。在本报告中,我们表明,Raf-1氨基末端14-3-3结合位点的突变使其激活MEK/ERK途径的能力与诱导细胞转化和分化的能力脱钩。在NIH 3T3成纤维细胞和COS-1细胞中,丝氨酸259的突变产生的Raf-1蛋白激活MEK/ERK途径的效率与v-Raf相同。然而,与v-Raf不同的是,RafS259突变体未能诱导转化。它们在NIH 3T3成纤维细胞中诱导形态改变并略微加速增殖,但在小鼠中不具有致瘤性,并且在测量接触抑制丧失或不依赖贴壁生长的转化试验中表现得与野生型Raf-1相似。奇怪的是,RafS259突变体抑制了由激活的MEK等位基因诱导的集落形成,这表明它们可以过度激活负反馈途径。在有丝分裂后鸡神经视网膜细胞的原代培养中,RafS259A能够将增殖维持在与膜靶向转化Raf-1蛋白RafCAAX所维持的水平相当的水平。相比之下,与RafCAAX相比,RafS259A在PC12细胞中只是一种较差的神经突形成诱导剂。因此,RafS259突变体在基因上使MEK/ERK激活与Raf-1诱导转化和分化的能力分离。结果进一步表明,RafS259突变体抑制了促进这些生物学过程所需的信号通路。