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Computational modeling of eukaryotic mRNA turnover

Published online by Cambridge University Press:  25 September 2001

DAN CAO
Affiliation:
Howard Hughes Medical Institute and Department of Molecular and Cellular Biology, University of Arizona, Tucson, Arizona 85721, USA
ROY PARKER
Affiliation:
Howard Hughes Medical Institute and Department of Molecular and Cellular Biology, University of Arizona, Tucson, Arizona 85721, USA
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Abstract

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.

Type
Research Article
Information
RNA , Volume 7 , Issue 9 , September 2001 , pp. 1192 - 1212
Copyright
2001 RNA Society

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