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A simple model for Lutz and Bujard’s controllable promoters and its application for analyzing a simple genetic oscillator

机译:Lutz和Bujard可控启动子的简单模型及其在分析简单遗传振荡器中的应用

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摘要

We develop an exact and flexible mathematical model for Lutz and Bujard’s controllable promoters. It can be used as a building block for modeling genetic systems based on them. Special attention is paid to deduce all the model parameters from reported (in vitro) experimental data. We validate our model by comparing the regulatory ranges measured in vivo by Lutz and Bujard against the ranges predicted by the model, and which are calculated as the reporter activity obtained under inducing conditions divided by the activity measured under maximal repression. In particular, we verify Bond et al. assertion that the cooperativity between two lac operators can be assumed to be negligible when their central base pairs are separated by 22 or 32 bp [Gene repression by minimal lac loops in vivo, Nucleic Acids Res, >38 (2010) 8072–8082]. Moreover, we also find that the probability that two repressors LacI bind to these operators at the same time can be assumed to be negligible as well. We finally use the model for the promoter PLlacO-1 to analyze a synthetic genetic oscillator recently build by Stricker et al. [A fast, robust and tunable synthetic gene oscillator, Nature, >456 (2008) 516–519].
机译:我们为Lutz和Bujard的可控启动子开发了精确而灵活的数学模型。它可以用作基于遗传系统建模的基础。要特别注意从报告的(体外)实验数据中推断所有模型参数。我们通过将Lutz和Bujard在体内测得的调节范围与模型预测的范围进行比较,验证了我们的模型,该范围被计算为诱导条件下获得的报道基因活性除以最大阻抑下测得的活性。特别是,我们验证Bond等人。断言,当两个lac操纵子的中央碱基对相隔22或32 bp时,它们的协同作用可以忽略不计[体内最小lac环对基因的抑制,Nucleic Acids Res,> 38 (2010年)8072–8082]。此外,我们还发现,两个阻遏物LacI同时与这些操纵子结合的概率也可以认为是微不足道的。我们最终将启动子PLlacO-1的模型用于分析Stricker等人最近建立的合成遗传振荡器。 [快速,健壮和可调的合成基因振荡器,自然,> 456 (2008)516-519]。

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