Bhattacharyya Roby P, Reményi Attila, Yeh Brian J, Lim Wendell A
Department of Cellular and Molecular Pharmacology, University of California, San Francisco, California 94143, USA.
Annu Rev Biochem. 2006;75:655-80. doi: 10.1146/annurev.biochem.75.103004.142710.
Living cells display complex signal processing behaviors, many of which are mediated by networks of proteins specialized for signal transduction. Here we focus on the question of how the remarkably diverse array of eukaryotic signaling circuits may have evolved. Many of the mechanisms that connect signaling proteins into networks are highly modular: The core catalytic activity of a signaling protein is physically and functionally separable from molecular domains or motifs that determine its linkage to both inputs and outputs. This high degree of modularity may make these systems more evolvable-in principle, novel circuits, and therefore highly innovative regulatory behaviors, can arise from relatively simple genetic events such as recombination, deletion, or insertion. In support of this hypothesis, recent studies show that such modular systems can be exploited to engineer nonnatural signaling proteins and pathways with novel behavior.
活细胞表现出复杂的信号处理行为,其中许多行为是由专门用于信号转导的蛋白质网络介导的。在这里,我们关注的问题是,真核生物信号传导回路这一极其多样的阵列是如何进化的。将信号蛋白连接成网络的许多机制具有高度模块化:信号蛋白的核心催化活性在物理和功能上与决定其与输入和输出连接的分子结构域或基序是可分离的。这种高度的模块化可能使这些系统更具可进化性——原则上,新的回路以及因此产生的高度创新的调控行为,可以源自相对简单的基因事件,如重组、缺失或插入。为支持这一假设,最近的研究表明,这种模块化系统可被用于设计具有新行为的非天然信号蛋白和信号通路。