Matheny Sharon A, White Michael A
Zimmer Biologics, Austin, Texas 78729, USA.
J Biol Chem. 2009 Apr 24;284(17):11007-11. doi: 10.1074/jbc.R800082200. Epub 2008 Dec 17.
The Ras effector and E3 ligase family member IMP (impedes mitogenic signal propagation) acts as a steady-state resistor within the Raf-MEK-ERK kinase module. IMP concentrations are directly regulated by Ras, through induction of autoubiquitination, to permit productive Raf-MEK complex assembly. Inhibition of Raf-MEK pathway activation by IMP occurs through the inactivation of KSR, a scaffold/adapter protein that couples activated Raf to its substrate MEK1. The capacity of IMP to inhibit signal propagation through Raf to MEK is, in part, a consequence of disrupting KSR1 homo-oligomerization and c-Raf-B-Raf hetero-oligomerization. These observations suggest that IMP functions as a threshold modulator, controlling sensitivity of the cascade to stimulus by directly limiting the assembly of functional KSR1-dependent Raf-MEK complexes.
Ras效应器和E3连接酶家族成员IMP(抑制有丝分裂信号传播)在Raf-MEK-ERK激酶模块中充当稳态电阻器。IMP的浓度由Ras直接调节,通过自泛素化的诱导,以允许形成有活性的Raf-MEK复合物。IMP对Raf-MEK途径激活的抑制是通过KSR(一种将活化的Raf与其底物MEK1偶联的支架/衔接蛋白)的失活来实现的。IMP抑制信号从Raf向MEK传播的能力,部分是破坏KSR1同源寡聚化和c-Raf-B-Raf异源寡聚化的结果。这些观察结果表明,IMP作为阈值调节剂,通过直接限制功能性KSR1依赖性Raf-MEK复合物的组装来控制级联对刺激的敏感性。