Murphy Leon O, Blenis John
Developmental and Molecular Pathways, Novartis Institutes for BioMedical Research, 250 Massachusetts Avenue, Cambridge, MA 02139, USA.
Trends Biochem Sci. 2006 May;31(5):268-75. doi: 10.1016/j.tibs.2006.03.009. Epub 2006 Apr 17.
Although the mechanisms that lead to activation of the Ras, extracellular-signal-regulated kinase mitogen-activated protein kinase (Ras/ERK-MAPK) signaling pathway have been studied intensively, the fundamental principles that determine how activation of ERK signaling can result in distinct biological outcomes have only recently received attention. Factors such as cell-surface receptor density, expression of scaffolding proteins, the surrounding extracellular matrix, and the interplay between kinases and phosphatases modulate the strength and duration of ERK signaling. Furthermore, the spatial distribution and temporal qualities of ERK can markedly alter the qualitative and quantitative features of downstream signaling to immediate early genes (IEG) and the expression of IEG-encoded protein products. As a result, IEG products provide a molecular interpretation of ERK dynamics, enabling the cell to program an appropriate biological response.
尽管导致Ras(一种原癌基因)、细胞外信号调节激酶丝裂原活化蛋白激酶(Ras/ERK-MAPK)信号通路激活的机制已得到深入研究,但决定ERK信号激活如何导致不同生物学结果的基本原理直到最近才受到关注。诸如细胞表面受体密度、支架蛋白表达、周围细胞外基质以及激酶与磷酸酶之间的相互作用等因素,会调节ERK信号的强度和持续时间。此外,ERK的空间分布和时间特性可显著改变对即刻早期基因(IEG)的下游信号传导的定性和定量特征,以及IEG编码蛋白产物的表达。因此,IEG产物为ERK动态变化提供了分子解读,使细胞能够规划适当的生物学反应。