Department of Microbiology and Immunology, Geisel School of Medicine at Dartmouth, Hanover, New Hampshire 03755; email:
Annu Rev Microbiol. 2017 Sep 8;71:179-195. doi: 10.1146/annurev-micro-090816-093325. Epub 2017 Jun 23.
Cyclic diguanylate (c-di-GMP) is a near universal signaling molecule produced by diguanylate cyclases that can direct a variety of bacterial behaviors. A major area of research over the last several years has been aimed at understanding how a cell with dozens of diguanylate cyclases can deploy a given subset of them to produce a desired phenotypic outcome without undesired cross talk between c-di-GMP-dependent systems. Several models have been put forward to address this question, including specificity of cyclase activation, tuned binding constants of effector proteins, and physical interaction between cyclases and effectors. Additionally, recent evidence has suggested that there may be a link between the catalytic state of a cyclase and its physical contact with an effector. This review highlights several key studies, examines the proposed global and local models of c-di-GMP signaling specificity in bacteria, and attempts to identify the most fruitful steps that can be taken to better understand how dynamic networks of sibling cyclases and effector proteins result in sensible outputs that govern cellular behavior.
环二鸟苷酸(c-di-GMP)是一种由双鸟苷酸环化酶产生的近普遍存在的信号分子,可以指导细菌的各种行为。过去几年来的一个主要研究领域是了解一个拥有数十种双鸟苷酸环化酶的细胞如何在没有 c-di-GMP 依赖性系统之间的不良串扰的情况下,选择特定的一组环化酶来产生所需的表型结果。已经提出了几种模型来解决这个问题,包括环化酶激活的特异性、效应蛋白结合常数的调节,以及环化酶和效应蛋白之间的物理相互作用。此外,最近的证据表明,环化酶的催化状态与其与效应蛋白的物理接触之间可能存在联系。本文综述了几项关键研究,考察了细菌中环二鸟苷酸信号特异性的全局和局部模型,并试图确定可以采取的最有成效的步骤,以更好地了解同胞环化酶和效应蛋白的动态网络如何产生控制细胞行为的合理输出。