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Modulation of gene transcription noise by competing transcription factors

机译:竞争性转录因子对基因转录噪声的调控

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摘要

Sequence specific transcription factors (TFs) are critical to ensuring that genes are transcribed in the right cell at the right time. Often, the gene promoter is flanked by multiple binding sites, some of which can be bound by different types of TFs in the cell. To investigate how the transcription noise is modulated by the competition of these TFs at their shared binding sites, we model gene transcription as a renewal process where the time spent in each transcription cycle is assumed to be independently and identically distributed. With the help of the elementary renewal theorem and the central limit theorem, we prove that the stationary noise strength Φ of transcription frequency equals the noise η ~2 of the time spent in a single transcription cycle. Subsequent analysis shows that competitive TF binding could produce an unbounded spectrum of Φ, in sharp contrast to the estimate 1/3 ≤Φ < 1 for single binding pattern activated transcription. We predict several mechanisms by which genes could stay away from abnormally noisy transcription while living with multiple binding patterns. The most efficient one is to maintain a relatively long engaged time by transcription pausing, interrupting, or other means. Alternatively, high noise strength is prevented if all binding patterns activate transcription strongly. When some binding patterns activate transcription weakly, low noise strength is ensured if the binding pattern with the weakest activation strength is utilized frequently.
机译:序列特异性转录因子(TFs)对于确保基因在正确的时间在正确的细胞中转录至关重要。通常,基因启动子的侧面是多个结合位点,其中一些可以与细胞中不同类型的TF结合。为了研究如何通过这些TF在它们共享的结合位点上的竞争来调节转录噪声,我们将基因转录建模为一个更新过程,其中假设每个转录周期所花费的时间是独立且相同地分布的。借助基本更新定理和中心极限定理,我们证明了转录频率的平稳噪声强度Φ等于单个转录周期中所花费时间的噪声η〜2。随后的分析表明,竞争性TF结合可产生无限制的Φ光谱,这与单结合模式激活转录的估计值1/3≤Φ<1形成鲜明对比。我们预测几种机制,通过这些机制,基因可以远离异常嘈杂的转录,同时具有多种结合模式。最有效的一种方法是通过暂停,中断或其他方式来保持相对较长的接合时间。或者,如果所有结合模式都强烈激活转录,则可以防止高噪音强度。当一些结合模式弱地激活转录时,如果频繁使用具有最弱激活强度的结合模式,则可确保低噪声强度。

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