Cao D, Parker R
Howard Hughes Medical Institute and Department of Molecular and Cellular Biology, University of Arizona, Tucson 85721, USA.
RNA. 2001 Sep;7(9):1192-212. doi: 10.1017/s1355838201010330.
The process of eukaryotic gene expression involves a diverse number of steps including transcription, RNA processing, transport, translation, and mRNA turnover. A critical step in understanding this process will be the development of mathematical models that quantitatively describe and predict the behavior of this complex system. We have simulated eukaryotic mRNA turnover in a linear multicomponent model based on the known mRNA decay pathways in yeast. Using rate constants based on experimental data for the yeast unstable MFA2 and stable PGK1 transcripts, the computational modeling reproduces experimental observations after minor adjustments. Subsequent analysis and a series of in silico experiments led to several conclusions. First, we demonstrate that mRNA half-life as commonly measured underestimates the average life span of an mRNA. Second, due to the properties of the pathways, the measurement of a half-life can predominantly measure different steps in the decay network. A corollary of this fact is that different mRNAs will be affected differentially by changes in specific rate constants. Third, the way to obtain the largest change of levels of mRNA for the smallest changes in rate is by changing the rate of deadenylation, where a large amount of regulation of mRNA decay occurs. Fourth, the 3'-to-5' degradation of mRNA shows mRNA-specific rates of degradation that are dependent on the 5' structure of the mRNA. These programs can be run over the Web, are adaptable to other eukaryotes, and provide outputs as graphs and virtual northern gels, which can be directly compared to experimental data. Therefore, this model constitutes a useful tool for the quantitative analysis of the process and control of mRNA degradation in eukaryotic cells.
真核基因表达过程涉及众多步骤,包括转录、RNA加工、转运、翻译以及mRNA周转。理解这一过程的关键步骤将是开发数学模型,以定量描述和预测这个复杂系统的行为。我们基于酵母中已知的mRNA衰变途径,在一个线性多组分模型中模拟了真核mRNA周转。利用基于酵母不稳定的MFA2和稳定的PGK1转录本实验数据的速率常数,经过微小调整后,计算模型重现了实验观察结果。后续分析和一系列计算机模拟实验得出了几个结论。首先,我们证明通常测量的mRNA半衰期低估了mRNA的平均寿命。其次,由于这些途径的特性,半衰期的测量主要可以测量衰变网络中的不同步骤。这一事实的一个推论是,不同的mRNA将受到特定速率常数变化的不同影响。第三,在速率变化最小的情况下获得mRNA水平最大变化的方法是改变去腺苷酸化速率,mRNA衰变的大量调控发生在此处。第四,mRNA的3'到5'降解显示出依赖于mRNA 5'结构的mRNA特异性降解速率。这些程序可以通过网络运行,适用于其他真核生物,并以图表和虚拟Northern杂交凝胶的形式提供输出结果,这些结果可以直接与实验数据进行比较。因此,该模型构成了定量分析真核细胞中mRNA降解过程和控制的有用工具。