Suderman Ryan, Deeds Eric J
Center for Computational Biology, University of Kansas, Lawrence, KS 66047, USA.
Department of Molecular Biosciences, University of Kansas, Lawrence, KS 66047, USA.
Interface Focus. 2018 Dec 6;8(6):20180039. doi: 10.1098/rsfs.2018.0039. Epub 2018 Oct 19.
All living things have evolved to sense changes in their environment in order to respond in adaptive ways. At the cellular level, these sensing systems generally involve receptor molecules at the cell surface, which detect changes outside the cell and relay those changes to the appropriate response elements downstream. With the advent of experimental technologies that can track signalling at the single-cell level, it has become clear that many signalling systems exhibit significant levels of 'noise,' manifesting as differential responses of otherwise identical cells to the same environment. This noise has a large impact on the capacity of cell signalling networks to transmit information from the environment. Application of information theory to experimental data has found that all systems studied to date encode less than 2.5 bits of information, with the majority transmitting significantly less than 1 bit. Given the growing interest in applying information theory to biological data, it is crucial to understand whether the low values observed to date represent some sort of intrinsic limit on information flow given the inherently stochastic nature of biochemical signalling events. In this work, we used a series of computational models to explore how much information a variety of common 'signalling motifs' can encode. We found that the majority of these motifs, which serve as the basic building blocks of cell signalling networks, can encode far more information (4-6 bits) than has ever been observed experimentally. In addition to providing a consistent framework for estimating information-theoretic quantities from experimental data, our findings suggest that the low levels of information flow observed so far in living system are not necessarily due to intrinsic limitations. Further experimental work will be needed to understand whether certain cell signalling systems actually can approach the intrinsic limits described here, and to understand the sources and purpose of the variation that reduces information flow in living cells.
所有生物都经过进化以感知环境变化,从而以适应性方式做出反应。在细胞水平上,这些传感系统通常涉及细胞表面的受体分子,它们检测细胞外的变化,并将这些变化传递给下游适当的反应元件。随着能够在单细胞水平追踪信号传导的实验技术的出现,很明显许多信号系统表现出显著水平的“噪声”,表现为原本相同的细胞对相同环境的不同反应。这种噪声对细胞信号网络从环境中传输信息的能力有很大影响。将信息论应用于实验数据发现,迄今为止研究的所有系统编码的信息都少于2.5比特,大多数系统传输的信息远少于1比特。鉴于将信息论应用于生物数据的兴趣日益浓厚,了解迄今为止观察到的低数值是否代表生化信号事件固有随机性所导致的信息流的某种内在限制至关重要。在这项工作中,我们使用了一系列计算模型来探索各种常见的“信号基序”能够编码多少信息。我们发现,这些作为细胞信号网络基本构建块的基序中的大多数能够编码比以往实验观察到的多得多的信息(4 - 6比特)。除了为从实验数据估计信息论量提供一个一致的框架外,我们的发现表明,迄今为止在生命系统中观察到的低信息流水平不一定是由于内在限制。需要进一步的实验工作来了解某些细胞信号系统是否真的能够接近这里描述的内在极限,以及了解减少活细胞中信息流的变化的来源和目的。