Inder Kerry, Harding Angus, Plowman Sarah J, Philips Mark R, Parton Robert G, Hancock John F
Institute for Molecular Bioscience, University of Queensland, Brisbane 4072, Australia.
Mol Biol Cell. 2008 Nov;19(11):4776-84. doi: 10.1091/mbc.e08-04-0407. Epub 2008 Sep 10.
The Ras/Raf/MEK/ERK (MAPK) pathway directs multiple cell fate decisions within a single cell. How different system outputs are generated is unknown. Here we explore whether activating the MAPK module from different membrane environments can rewire system output. We identify two classes of nanoscale environment within the plasma membrane. The first, which corresponds to nanoclusters occupied by GTP-loaded H-, N- or K-Ras, supports Raf activation and amplifies low Raf kinase input to generate a digital ERKpp output. The second class, which corresponds to nanoclusters occupied by GDP-loaded Ras, cannot activate Raf and therefore does not activate the MAPK module, illustrating how lateral segregation on plasma membrane influences signal output. The MAPK module is activated at the Golgi, but in striking contrast to the plasma membrane, ERKpp output is analog. Different modes of Raf activation precisely correlate with these different ERKpp system outputs. Intriguingly, the Golgi contains two distinct membrane environments that generate ERKpp, but only one is competent to drive PC12 cell differentiation. The MAPK module is not activated from the ER. Taken together these data clearly demonstrate that the different nanoscale environments available to Ras generate distinct circuit configurations for the MAPK module, bestowing cells with a simple mechanism to generate multiple system outputs from a single cascade.
Ras/Raf/MEK/ERK(丝裂原活化蛋白激酶)信号通路指导单个细胞内的多种细胞命运决定。不同的系统输出是如何产生的尚不清楚。在这里,我们探讨从不同的膜环境激活丝裂原活化蛋白激酶模块是否能重新连接系统输出。我们在质膜内确定了两类纳米级环境。第一类对应于由结合GTP的H-Ras、N-Ras或K-Ras占据的纳米簇,支持Raf激活并放大低水平的Raf激酶输入以产生数字式的细胞外信号调节激酶磷酸化(ERKpp)输出。第二类对应于由结合GDP的Ras占据的纳米簇,不能激活Raf,因此也不能激活丝裂原活化蛋白激酶模块,这说明了质膜上的侧向分离如何影响信号输出。丝裂原活化蛋白激酶模块在高尔基体被激活,但与质膜形成鲜明对比的是,ERKpp输出是模拟式的。不同的Raf激活模式与这些不同的ERKpp系统输出精确相关。有趣的是,高尔基体包含两种不同的膜环境可产生ERKpp,但只有一种能够驱动PC12细胞分化。丝裂原活化蛋白激酶模块不会从内质网被激活。综上所述,这些数据清楚地表明,Ras可利用的不同纳米级环境为丝裂原活化蛋白激酶模块产生了不同的电路配置,赋予细胞一种简单的机制,使其能从单个级联反应中产生多种系统输出。