Program in Developmental Biology, Sloan-Kettering Institute, Memorial Sloan-Kettering Cancer Center, New York, New York, United States of America; Instituto de Neurosciencias de Alicante, Consejo Superior de Investigaciones Científicas/University Miguel Hernandez, Unidad de Neurobiología del Desarrollo, Alicante, Spain.
PLoS One. 2006 Dec 20;1(1):e66. doi: 10.1371/journal.pone.0000066.
Over the past few years, it has become increasingly apparent that signal transduction pathways are not merely linear cascades; they are organized into complex signaling networks that require high levels of regulation to generate precise and unique cell responses. However, the underlying regulatory mechanisms by which signaling pathways cross-communicate remain poorly understood. Here we show that the Ras-binding protein Canoe (Cno)/AF-6, a PDZ protein normally associated with cellular junctions, is a key modulator of Wingless (Wg)/Wnt, Ras-Mitogen Activated Protein Kinase (MAPK) and Notch (N) signaling pathways cross-communication. Our data show a repressive effect of Cno/AF-6 on these three signaling pathways through physical interactions with Ras, N and the cytoplasmic protein Dishevelled (Dsh), a key Wg effector. We propose a model in which Cno, through those interactions, actively coordinates, at the membrane level, Ras-MAPK, N and Wg signaling pathways during progenitor specification.
在过去的几年中,越来越明显的是,信号转导途径不仅仅是线性级联;它们被组织成复杂的信号网络,需要高水平的调节才能产生精确和独特的细胞反应。然而,信号通路交叉通讯的潜在调节机制仍知之甚少。在这里,我们表明 Ras 结合蛋白 Canoe(Cno)/AF-6,一种通常与细胞连接相关的 PDZ 蛋白,是 Wingless(Wg)/Wnt、Ras-MAPK 和 Notch(N)信号通路交叉通讯的关键调节剂。我们的数据表明,Cno/AF-6 通过与 Ras、N 和细胞质蛋白 Dishevelled(Dsh)的物理相互作用,对这三个信号通路产生抑制作用,Dsh 是 Wg 的关键效应物。我们提出了一个模型,其中 Cno 通过这些相互作用,在膜水平上主动协调祖细胞特化过程中的 Ras-MAPK、N 和 Wg 信号通路。