Department of Cellular and Molecular Pharmacology, University of California, San Francisco, 600 16th Street, San Francisco, CA 94158, USA; Howard Hughes Medical Institute, University of California, San Francisco, San Francisco, CA 94158, USA.
Department of Cellular and Molecular Pharmacology, University of California, San Francisco, 600 16th Street, San Francisco, CA 94158, USA; Howard Hughes Medical Institute, University of California, San Francisco, San Francisco, CA 94158, USA; Cell Design Initiative, University of California, San Francisco, San Francisco, CA 94158, USA.
Cell Syst. 2019 Sep 25;9(3):297-308.e2. doi: 10.1016/j.cels.2019.07.008. Epub 2019 Sep 11.
Many cellular responses for which timing is critical display temporal filtering-the ability to suppress response until stimulated for longer than a given minimal time. To identify biochemical circuits capable of kinetic filtering, we comprehensively searched the space of three-node enzymatic networks. We define a metric of "temporal ultrasensitivity," the steepness of activation as a function of stimulus duration. We identified five classes of core network motifs capable of temporal filtering, each with distinct functional properties such as rejecting high-frequency noise, committing to response (bistability), and distinguishing between long stimuli. Combinations of the two most robust motifs, double inhibition (DI) and positive feedback with AND logic (PF), underlie several natural timer circuits involved in processes such as cell cycle transitions, T cell activation, and departure from the pluripotent state. The biochemical network motifs described in this study form a basis for understanding common ways cells make dynamic decisions.
许多对时间敏感的细胞反应表现出时间滤波的能力——即在受到刺激超过给定最小时间之前,抑制反应的能力。为了识别能够进行动力学滤波的生化电路,我们全面搜索了三节点酶网络的空间。我们定义了“时间超敏性”的度量标准,即作为刺激持续时间函数的激活陡峭度。我们确定了五类能够进行时间滤波的核心网络基元,每个基元都具有不同的功能特性,例如拒绝高频噪声、响应承诺(双稳性)和区分长刺激。两种最稳健的基元——双抑制(DI)和具有 AND 逻辑的正反馈(PF)的组合——是参与细胞周期转换、T 细胞激活和从多能状态脱离等过程的几个自然计时器电路的基础。本研究中描述的生化网络基元为理解细胞做出动态决策的常见方式提供了基础。