Shaul Yoav D, Seger Rony
Department of Biological Regulation, The Weizmann Institute of Science, 76100 Rehovot, Israel.
Biochim Biophys Acta. 2007 Aug;1773(8):1213-26. doi: 10.1016/j.bbamcr.2006.10.005. Epub 2006 Oct 19.
The ERK signaling cascade is a central MAPK pathway that plays a role in the regulation of various cellular processes such as proliferation, differentiation, development, learning, survival and, under some conditions, also apoptosis. The ability of this cascade to regulate so many distinct, and even opposing, cellular processes, raises the question of signaling specificity determination by this cascade. Here we describe mechanisms that cooperate to direct MEK-ERK signals to their appropriate downstream destinations. These include duration and strength of the signals, interaction with specific scaffolds, changes in subcellular localization, crosstalk with other signaling pathways, and presence of multiple components with distinct functions in each tier of the cascade. Since many of the mechanisms do not function properly in cancer cells, understanding them may shed light not only on the regulation of normal cell proliferation, but also on mechanisms of oncogenic transformation.
ERK信号级联是一条核心的丝裂原活化蛋白激酶(MAPK)通路,在多种细胞过程的调控中发挥作用,如增殖、分化、发育、学习、存活,并且在某些情况下还参与细胞凋亡。该信号级联能够调控如此众多不同甚至相反的细胞过程,这就引发了关于其信号特异性决定机制的问题。在此,我们描述了协同作用将MEK-ERK信号导向其适当下游靶点的机制。这些机制包括信号的持续时间和强度、与特定支架的相互作用、亚细胞定位的变化、与其他信号通路的串扰,以及在信号级联的每一层中存在具有不同功能的多个组分。由于许多机制在癌细胞中不能正常发挥作用,对它们的理解不仅可能有助于阐明正常细胞增殖的调控机制,还能揭示致癌转化的机制。