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2
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本文引用的文献

1
Using plasma membrane nanoclusters to build better signaling circuits.利用质膜纳米簇构建更好的信号传导回路。
Trends Cell Biol. 2008 Aug;18(8):364-71. doi: 10.1016/j.tcb.2008.05.006. Epub 2008 Jul 10.
2
Electrostatic interactions positively regulate K-Ras nanocluster formation and function.静电相互作用正向调节K-Ras纳米簇的形成与功能。
Mol Cell Biol. 2008 Jul;28(13):4377-85. doi: 10.1128/MCB.00050-08. Epub 2008 May 5.
3
A novel switch region regulates H-ras membrane orientation and signal output.一个新的开关区域调节H-ras膜方向和信号输出。
EMBO J. 2008 Mar 5;27(5):727-35. doi: 10.1038/emboj.2008.10. Epub 2008 Feb 14.
4
Ras nanoclusters: combining digital and analog signaling.Ras纳米簇:数字信号与模拟信号的结合
Cell Cycle. 2008 Jan 15;7(2):127-34. doi: 10.4161/cc.7.2.5237. Epub 2007 Oct 26.
5
Palmitoylation and localisation of RAS isoforms are modulated by the hypervariable linker domain.RAS亚型的棕榈酰化和定位受高变连接域调控。
J Cell Sci. 2008 Feb 15;121(Pt 4):421-7. doi: 10.1242/jcs.020107. Epub 2008 Jan 22.
6
Spatial regulation of Raf kinase signaling by RKTG.RKTG对Raf激酶信号传导的空间调控
Proc Natl Acad Sci U S A. 2007 Sep 4;104(36):14348-53. doi: 10.1073/pnas.0701298104. Epub 2007 Aug 27.
7
Plasma membrane nanoswitches generate high-fidelity Ras signal transduction.质膜纳米开关可产生高保真的Ras信号转导。
Nat Cell Biol. 2007 Aug;9(8):905-14. doi: 10.1038/ncb1615. Epub 2007 Jul 8.
8
Integrating signals from RTKs to ERK/MAPK.整合从受体酪氨酸激酶到细胞外信号调节激酶/丝裂原活化蛋白激酶的信号。
Oncogene. 2007 May 14;26(22):3113-21. doi: 10.1038/sj.onc.1210394.
9
Growth factor-induced MAPK network topology shapes Erk response determining PC-12 cell fate.生长因子诱导的MAPK网络拓扑结构塑造决定PC-12细胞命运的Erk反应。
Nat Cell Biol. 2007 Mar;9(3):324-30. doi: 10.1038/ncb1543. Epub 2007 Feb 18.
10
CK2 Is a component of the KSR1 scaffold complex that contributes to Raf kinase activation.CK2是KSR1支架复合物的一个组成部分,该复合物有助于Raf激酶的激活。
Curr Biol. 2007 Jan 23;17(2):179-84. doi: 10.1016/j.cub.2006.11.061. Epub 2006 Dec 14.

从不同空间位置激活丝裂原活化蛋白激酶模块会产生不同的系统输出。

Activation of the MAPK module from different spatial locations generates distinct system outputs.

作者信息

Inder Kerry, Harding Angus, Plowman Sarah J, Philips Mark R, Parton Robert G, Hancock John F

机构信息

Institute for Molecular Bioscience, University of Queensland, Brisbane 4072, Australia.

出版信息

Mol Biol Cell. 2008 Nov;19(11):4776-84. doi: 10.1091/mbc.e08-04-0407. Epub 2008 Sep 10.

DOI:10.1091/mbc.e08-04-0407
PMID:18784252
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2575182/
Abstract

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.

摘要

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。