Computational modeling of eukaryotic mRNA turnover
- 25 September 2001
- journal article
- research article
- Published by Cold Spring Harbor Laboratory in RNA
- Vol. 7 (9) , 1192-1212
- https://doi.org/10.1017/s1355838201010330
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.Keywords
This publication has 72 references indexed in Scilit:
- Defects in the mRNA export factors Rat7p, Gle1p, Mex67p, and Rat8p cause hyperadenylation during 3′-end formation of nascent transcriptsRNA, 2001
- Functional interactions in internal translation initiation directed by viral and cellular IRES elementsJournal of General Virology, 2001
- Bidirectional RNA helicase activity of eucaryotic translation initiation factors 4A and 4F.Molecular and Cellular Biology, 1990
- Immunoblot analysis of the structure of protein synthesis initiation factor eIF3 from HeLa cellsArchives of Biochemistry and Biophysics, 1990
- Internal initiation of translation of eukaryotic mRNA directed by a sequence derived from poliovirus RNANature, 1988
- Eukaryotic transient-expression system based on recombinant vaccinia virus that synthesizes bacteriophage T7 RNA polymerase.Proceedings of the National Academy of Sciences, 1986
- Eukaryotic protein synthesis initiation factor eIF-3: Determination of concentration and association with ribosomes in rabbit reticulocyte and HeLa cell lysatesBiochimica et Biophysica Acta (BBA) - Gene Structure and Expression, 1985
- Identification and quantitation of levels of protein synthesis initiation factors in crude HeLa cell lysates by two-dimensional polyacrylamide gel electrophoresis.Journal of Biological Chemistry, 1983
- Immunochemical characterization of mammalian protein synthesis initiation factorsBiochemistry, 1982
- Specific interaction of one subunit of eukaryotic initiation factor eIF-3 with 18S ribosomal RNA within the binary complex, eIF-3.small ribosomal subunit, as shown by cross-linking experimentsNucleic Acids Research, 1982