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Measuring the degree of modularity in gene regulatory networks from the relaxation of finite perturbations

机译:通过有限扰动的松弛来测量基因调控网络中的模块化程度

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In gene regulatory networks, transcription factors regulate downstream sites by binding or unbinding to specific promoter regions. It is known that the binding-unbinding process can affect factor life times, and thus response times. This change in the dynamical properties depends on the number of sites that the transcription factor binds to as well as the factor concentration level. To estimate how the dynamics of a given transcription factor will be affected by the number of binding sites, we previously devised a measure called the fan-out - complimentary measure to retroactivity - that indicates the maximum number of the binding sites before the dynamic response is significantly affected. We provided an efficient method to measure the fan-out and retroactivity experimentally by exploiting gene expression noise. In this presentation, we provide another efficient measurement method for retroactivity and fan-out at the population level. The method resorts to finite-size perturbations in system parameters or concentrations. The equivalent analysis method at the single cell level that is based on gene expression noise is also presented.
机译:在基因调节网络中,转录因子通过与特定启动子区域结合或不结合来调节下游位点。众所周知,绑定-解绑定过程会影响因子的寿命,从而影响响应时间。动力学特性的这种变化取决于转录因子结合的位点数量以及因子浓度水平。为了估计给定转录因子的动力学将如何受结合位点数目的影响,我们先前设计了一种称为扇出的措施-追溯性的互补措施-指示动态响应发生之前结合位点的最大数目。受到很大影响。我们提供了一种有效的方法,可以通过利用基因表达噪声来实验性地测量扇出和追溯性。在此演示文稿中,我们提供了另一种有效的测量方法,可用于总体水平的追溯性和扇出度。该方法诉诸于系统参数或浓度的有限大小扰动。还提出了基于基因表达噪声的单细胞水平等效分析方法。

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