Literature DB >> 11565744

Computational modeling of eukaryotic mRNA turnover.

D Cao1, R Parker.   

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.

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Year:  2001        PMID: 11565744      PMCID: PMC1370166          DOI: 10.1017/s1355838201010330

Source DB:  PubMed          Journal:  RNA        ISSN: 1355-8382            Impact factor:   4.942


  85 in total

Review 1.  Functional interactions in internal translation initiation directed by viral and cellular IRES elements.

Authors:  Encarnación Martínez-Salas; Ricardo Ramos; Esther Lafuente; Sonia López de Quinto
Journal:  J Gen Virol       Date:  2001-05       Impact factor: 3.891

2.  Defects in the mRNA export factors Rat7p, Gle1p, Mex67p, and Rat8p cause hyperadenylation during 3'-end formation of nascent transcripts.

Authors:  P Hilleren; R Parker
Journal:  RNA       Date:  2001-05       Impact factor: 4.942

3.  Eukaryotic transient-expression system based on recombinant vaccinia virus that synthesizes bacteriophage T7 RNA polymerase.

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Journal:  Proc Natl Acad Sci U S A       Date:  1986-11       Impact factor: 11.205

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Journal:  Arch Biochem Biophys       Date:  1990-01       Impact factor: 4.013

5.  A segment of the 5' nontranslated region of encephalomyocarditis virus RNA directs internal entry of ribosomes during in vitro translation.

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Journal:  J Virol       Date:  1988-08       Impact factor: 5.103

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Journal:  Biochemistry       Date:  1982-08-31       Impact factor: 3.162

7.  Eukaryotic protein synthesis initiation factor eIF-3: determination of concentration and association with ribosomes in rabbit reticulocyte and HeLa cell lysates.

Authors:  G Mengod; H Trachsel
Journal:  Biochim Biophys Acta       Date:  1985-06-24

8.  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 experiments.

Authors:  O Nygård; P Westermann
Journal:  Nucleic Acids Res       Date:  1982-02-25       Impact factor: 16.971

9.  Identification and quantitation of levels of protein synthesis initiation factors in crude HeLa cell lysates by two-dimensional polyacrylamide gel electrophoresis.

Authors:  R Duncan; J W Hershey
Journal:  J Biol Chem       Date:  1983-06-10       Impact factor: 5.157

10.  Internal initiation of translation of eukaryotic mRNA directed by a sequence derived from poliovirus RNA.

Authors:  J Pelletier; N Sonenberg
Journal:  Nature       Date:  1988-07-28       Impact factor: 49.962

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  55 in total

1.  RiboSys, a high-resolution, quantitative approach to measure the in vivo kinetics of pre-mRNA splicing and 3'-end processing in Saccharomyces cerevisiae.

Authors:  Ross D Alexander; J David Barrass; Beatriz Dichtl; Martin Kos; Tomasz Obtulowicz; Marie-Cecile Robert; Michal Koper; Iwona Karkusiewicz; Luisa Mariconti; David Tollervey; Bernhard Dichtl; Joanna Kufel; Edouard Bertrand; Jean D Beggs
Journal:  RNA       Date:  2010-10-25       Impact factor: 4.942

2.  Genome-wide analysis of mRNA stability using transcription inhibitors and microarrays reveals posttranscriptional control of ribosome biogenesis factors.

Authors:  Jörg Grigull; Sanie Mnaimneh; Jeffrey Pootoolal; Mark D Robinson; Timothy R Hughes
Journal:  Mol Cell Biol       Date:  2004-06       Impact factor: 4.272

3.  Phosphorylation of tristetraprolin by MK2 impairs AU-rich element mRNA decay by preventing deadenylase recruitment.

Authors:  Sandra L Clement; Claudia Scheckel; Georg Stoecklin; Jens Lykke-Andersen
Journal:  Mol Cell Biol       Date:  2010-11-15       Impact factor: 4.272

4.  The yeast EDC1 mRNA undergoes deadenylation-independent decapping stimulated by Not2p, Not4p, and Not5p.

Authors:  Denise Muhlrad; Roy Parker
Journal:  EMBO J       Date:  2005-02-10       Impact factor: 11.598

5.  Sbp1p affects translational repression and decapping in Saccharomyces cerevisiae.

Authors:  Scott P Segal; Travis Dunckley; Roy Parker
Journal:  Mol Cell Biol       Date:  2006-07       Impact factor: 4.272

6.  Yeast transcripts cleaved by an internal ribozyme provide new insight into the role of the cap and poly(A) tail in translation and mRNA decay.

Authors:  Stacie Meaux; Ambro Van Hoof
Journal:  RNA       Date:  2006-05-19       Impact factor: 4.942

7.  Packaging of the virion host shutoff (Vhs) protein of herpes simplex virus: two forms of the Vhs polypeptide are associated with intranuclear B and C capsids, but only one is associated with enveloped virions.

Authors:  G Sullivan Read; Mary Patterson
Journal:  J Virol       Date:  2006-11-08       Impact factor: 5.103

8.  Pat1 contains distinct functional domains that promote P-body assembly and activation of decapping.

Authors:  Guy R Pilkington; Roy Parker
Journal:  Mol Cell Biol       Date:  2007-12-17       Impact factor: 4.272

Review 9.  Deadenylation and P-bodies.

Authors:  Chyi-Ying A Chen; Ann-Bin Shyu
Journal:  Adv Exp Med Biol       Date:  2013       Impact factor: 2.622

10.  mRNA deadenylation by PARN is essential for embryogenesis in higher plants.

Authors:  Sergei V Reverdatto; James A Dutko; Julia A Chekanova; Douglas A Hamilton; Dmitry A Belostotsky
Journal:  RNA       Date:  2004-07-09       Impact factor: 4.942

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