昼夜节律稳健性分析的系统生物学方法

F. Doyle
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引用次数: 1

摘要

只提供摘要形式。理解调控是解开复杂生物系统的关键障碍。随着基因水平的结构逐渐为人所知,公开的挑战是将可预测的行为分配给已知的结构,即所谓的“基因型到表型”问题。为了应对这一挑战,系统生物学学科以一种综合的视角出现,以确定复杂系统的行为。一个特别有趣的特性是生物物理网络的鲁棒性:在存在不确定性和/或扰动的情况下保持某种目标水平的行为或性能的能力。在生物系统中,这些干扰可以是环境(热,pH等)或生物固有的(动力学参数的变化)。虽然对简单的(低维的,确定性的)生物系统有初步的结果,但分析这些权衡的通用工具是积极研究的主题。作为昼夜节律基础的基因网络是鲁棒性研究的理想系统,因为它在高度不确定的环境中表现出色。在控制理论分析中,果蝇的假设结构的主要元素包括嵌套的负自我调节反馈回路,控制着永恒(tim)和周期(per)的表达,与通过dClock基因建立的正反馈回路互锁。复杂的形成,调控易位和降解这些基因产物中的一些,这是额外的控制(和延迟)由蛋白质磷酸化,增加了系统的复杂性的进一步水平。在这次演讲中,系统理论中的一些定量工具被提出作为揭示健壮的生物调控系统的使能方法,重点是敏感性分析。我们对果蝇昼夜节律基因网络的建模和分析工作进行了详细的介绍,并对哺乳动物的类似物和更一般的基因调控网络进行了概括。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A system biology approach to robustness analysis of circadian rhythm
Summary form only given. Understanding regulation is a critical hurdle in unraveling complex biological systems. As gene-level architectures become known, the open challenge is to assign predictable behavior to a known structure, the so-called "genotype-to-phenotype" problem. In response to this challenge, the discipline of systems biology has emerged with an integrative perspective towards determining complex systems behavior. A property of particular interest is the robustness of the biophysical network: the ability to maintain some target level of behavior or performance in the presence of uncertainty and/or perturbations. In biological systems, these disturbances can be environmental (heat, pH, etc.) or intrinsic to the organism (changes in kinetic parameters). While preliminary results are available for simple (low-dimensional, deterministic) biological systems, general tools for analyzing these tradeoffs are the subject of active research. The gene network which underlies circadian rhythms is an ideal system for robustness studies, owing to its remarkable performance in a highly uncertain environment. Of interest for control theoretic analyses, the dominant elements of the postulated architecture for Drosophila consist of nested negative autoregulatory feedback loops controlling the expression of timeless (tim) and period (per) interlocked with a positive feedback loop established via the dClock gene. Complex formation, regulated translocation and degradation of several of these gene products, which is additionally controlled (and delayed) by protein phosphorylation, add further levels of complexity to the system. In this talk, a number of quantitative tools from systems theory are presented as enabling methodologies for unraveling robust biological regulatory systems, with an emphasis on sensitivity analysis. Our work on modeling and analysis of the Drosophila circadian rhythm gene network are detailed, and generalizations are be drawn for the mammalian analog and for more general gene regulatory networks.
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