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本文引用的文献

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Theoretical and experimental dissection of DNA loop-mediated repression.DNA 环介导抑制的理论和实验剖析。
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DNA looping in prokaryotes: experimental and theoretical approaches.原核生物中的 DNA 环化:实验和理论方法。
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Tuning promoter strength through RNA polymerase binding site design in Escherichia coli.通过 RNA 聚合酶结合位点设计在大肠杆菌中调节启动子强度。
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Operator sequence alters gene expression independently of transcription factor occupancy in bacteria.操作序列独立于转录因子占据改变细菌中的基因表达。
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A regulatory role for repeated decoy transcription factor binding sites in target gene expression.重复诱饵转录因子结合位点在靶基因表达中的调控作用。
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Gene regulatory logic for reading the Sonic Hedgehog signaling gradient in the vertebrate neural tube.脊椎动物神经管中 Sonic Hedgehog 信号梯度的基因调控逻辑。
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由于转录因子滴定导致多个启动子耦合转录的统计力学模型。

Statistical mechanical model of coupled transcription from multiple promoters due to transcription factor titration.

作者信息

Rydenfelt Mattias, Cox Robert Sidney, Garcia Hernan, Phillips Rob

机构信息

Department of Physics, California Institute of Technology, Pasadena, California 91125, USA.

Technology Research Association of Highly Efficient Gene Design, Kobe University, Hyogo 657-8501, Japan.

出版信息

Phys Rev E Stat Nonlin Soft Matter Phys. 2014 Jan;89(1):012702. doi: 10.1103/PhysRevE.89.012702. Epub 2014 Jan 6.

DOI:10.1103/PhysRevE.89.012702
PMID:24580252
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4043999/
Abstract

Transcription factors (TFs) with regulatory action at multiple promoter targets is the rule rather than the exception, with examples ranging from the cAMP receptor protein (CRP) in E. coli that regulates hundreds of different genes simultaneously to situations involving multiple copies of the same gene, such as plasmids, retrotransposons, or highly replicated viral DNA. When the number of TFs heavily exceeds the number of binding sites, TF binding to each promoter can be regarded as independent. However, when the number of TF molecules is comparable to the number of binding sites, TF titration will result in correlation ("promoter entanglement") between transcription of different genes. We develop a statistical mechanical model which takes the TF titration effect into account and use it to predict both the level of gene expression for a general set of promoters and the resulting correlation in transcription rates of different genes. Our results show that the TF titration effect could be important for understanding gene expression in many regulatory settings.

摘要

在多个启动子靶点具有调控作用的转录因子(TFs)是普遍现象而非个别情况,实例包括大肠杆菌中的环磷酸腺苷受体蛋白(CRP),它能同时调控数百个不同基因,以及涉及同一基因多个拷贝的情况,如质粒、逆转录转座子或高度复制的病毒DNA。当转录因子的数量大大超过结合位点的数量时,转录因子与每个启动子的结合可视为独立的。然而,当转录因子分子的数量与结合位点的数量相当,转录因子滴定将导致不同基因转录之间的相关性(“启动子纠缠”)。我们开发了一个统计力学模型,该模型考虑了转录因子滴定效应,并用它来预测一组通用启动子的基因表达水平以及不同基因转录速率之间的相关性。我们的结果表明,转录因子滴定效应对于理解许多调控环境中的基因表达可能很重要。