Department of Mathematics, Uppsala University, SE-751 06 Uppsala, Sweden.
Nat Commun. 2011 Aug 9;2:419. doi: 10.1038/ncomms1422.
Direct negative feedback decreases fluctuations and is a ubiquitous mechanism for homoeostatic control. However, intracellular regulation frequently operates indirectly, resulting in delayed responses. Here we derive an analytical expression that quantifies the consequences from delayed negative feedback resulting from typical multistep synthesis pathways, for example, transcription or translation. We find that indirect feedback leads to more fluctuations than without feedback for intermediate delays, but surprisingly not for long delays. The anomalous fluctuations at intermediate delays emerge from positive correlations between the delayed regulatory events, and are shown to be equivalent to an increased stoichiometry in the synthesis of new molecules. The results primarily give us insight about the design principles of delayed stochastic control systems and why a fixed feedback delay gives more fluctuations than a broadly distributed feedback delay. It is also shown that the feedback delay of auto-repressed regulators can result in more sensitive regulation of downstream processes through stochastic focusing.
直接负反馈可减少波动,是内稳态控制的普遍机制。然而,细胞内的调节常常是间接进行的,导致响应延迟。在这里,我们推导出一个解析表达式,用于量化典型多步合成途径(如转录或翻译)中延迟负反馈的后果。我们发现,间接反馈会导致中间延迟时的波动比没有反馈时更大,但奇怪的是,长延迟时则不是。中间延迟的异常波动源自延迟调节事件之间的正相关,并且被证明相当于新分子合成中增加了化学计量。这些结果主要让我们了解延迟随机控制系统的设计原则,以及为什么固定的反馈延迟会比广泛分布的反馈延迟产生更多的波动。还表明,自动抑制调节因子的反馈延迟可以通过随机聚焦导致下游过程的更敏感调节。