Department of Theory and Bio-Systems, Max Planck Institute of Colloids and Interfaces, D-14424 Potsdam, Germany.
Phys Biol. 2013 Aug;10(4):046008. doi: 10.1088/1478-3975/10/4/046008. Epub 2013 Jul 24.
Based on the experimental evidence that translating ribosomes stabilize the mRNAs, we introduce and study a theoretical model for the dynamic shielding of mRNA by ribosomes. We present an improved fitting of published decay assay data in E. coli and show that only one third of the decay patterns are exponential. Our new transcriptome-wide estimate of the average lifetimes and mRNA half-lives shows that these timescales are considerably shorter than previous estimates. We also explain why there is a negative correlation between mRNA length and average lifetime when the mRNAs are subdivided in classes sharing the same degradation parameters. As a by-product, our model indicates that co-transcriptional translation in E. coli may be less common than previously believed.
基于核糖体稳定 mRNA 的实验证据,我们引入并研究了核糖体对 mRNA 动态屏蔽的理论模型。我们对发表的大肠杆菌衰减测定数据进行了改进拟合,并表明只有三分之一的衰减模式是指数衰减。我们对转录组范围内平均寿命和 mRNA 半衰期的新估计表明,这些时间尺度比以前的估计要短得多。我们还解释了为什么当 mRNAs 按照具有相同降解参数的类别细分时,mRNA 长度与平均寿命之间存在负相关。作为副产品,我们的模型表明,原核生物中的共转录翻译可能比以前认为的不那么普遍。