Literature DB >> 11101532

The Puf3 protein is a transcript-specific regulator of mRNA degradation in yeast.

W Olivas1, R Parker.   

Abstract

Eukaryotic post-transcriptional regulation is often specified by control elements within mRNA 3'- untranslated regions (3'-UTRs). In order to identify proteins that regulate specific mRNA decay rates in Saccharomyces cerevisae, we analyzed the role of five members of the Puf family present in the yeast genome (referred to as JSN1/PUF1, PUF2, PUF3, PUF4 and MPT5/PUF5). Yeast strains lacking all five Puf proteins showed differential expression of numerous yeast mRNAs. Examination of COX17 mRNA indicates that Puf3p specifically promotes decay of this mRNA by enhancing the rate of deadenylation and subsequent turnover. Puf3p also binds to the COX17 mRNA 3'-UTR in vitro. This indicates that the function of Puf proteins as specific regulators of mRNA deadenylation has been conserved throughout eukaryotes. In contrast to the case in Caenorhabditis elegans and Drosophila, yeast Puf3p does not affect translation of COX17 mRNA. These observations indicate that Puf proteins are likely to play a role in the control of transcript-specific rates of degradation in yeast by interacting directly with the mRNA turnover machinery.

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Year:  2000        PMID: 11101532      PMCID: PMC305854          DOI: 10.1093/emboj/19.23.6602

Source DB:  PubMed          Journal:  EMBO J        ISSN: 0261-4189            Impact factor:   11.598


  44 in total

1.  mRNA decapping in yeast requires dissociation of the cap binding protein, eukaryotic translation initiation factor 4E.

Authors:  D C Schwartz; R Parker
Journal:  Mol Cell Biol       Date:  2000-11       Impact factor: 4.272

2.  Two distinct destabilizing elements in the c-fos message trigger deadenylation as a first step in rapid mRNA decay.

Authors:  A B Shyu; J G Belasco; M E Greenberg
Journal:  Genes Dev       Date:  1991-02       Impact factor: 11.361

3.  The most abundant small cytoplasmic RNA of Saccharomyces cerevisiae has an important function required for normal cell growth.

Authors:  F Felici; G Cesareni; J M Hughes
Journal:  Mol Cell Biol       Date:  1989-08       Impact factor: 4.272

4.  Recruitment of Nanos to hunchback mRNA by Pumilio.

Authors:  J Sonoda; R P Wharton
Journal:  Genes Dev       Date:  1999-10-15       Impact factor: 11.361

5.  Maternal Pumilio acts together with Nanos in germline development in Drosophila embryos.

Authors:  M Asaoka-Taguchi; M Yamada; A Nakamura; K Hanyu; S Kobayashi
Journal:  Nat Cell Biol       Date:  1999-11       Impact factor: 28.824

6.  Glucose-regulated turnover of mRNA and the influence of poly(A) tail length on half-life.

Authors:  S Prieto; B J de la Cruz; I E Scheffler
Journal:  J Biol Chem       Date:  2000-05-12       Impact factor: 5.157

7.  Mammalian glucocorticoid receptor derivatives enhance transcription in yeast.

Authors:  M Schena; K R Yamamoto
Journal:  Science       Date:  1988-08-19       Impact factor: 47.728

Review 8.  Mechanisms and control of mRNA decapping in Saccharomyces cerevisiae.

Authors:  M Tucker; R Parker
Journal:  Annu Rev Biochem       Date:  2000       Impact factor: 23.643

9.  Identification and comparison of stable and unstable mRNAs in Saccharomyces cerevisiae.

Authors:  D Herrick; R Parker; A Jacobson
Journal:  Mol Cell Biol       Date:  1990-05       Impact factor: 4.272

10.  Binding of pumilio to maternal hunchback mRNA is required for posterior patterning in Drosophila embryos.

Authors:  Y Murata; R P Wharton
Journal:  Cell       Date:  1995-03-10       Impact factor: 41.582

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  134 in total

1.  Computational modeling of eukaryotic mRNA turnover.

Authors:  D Cao; R Parker
Journal:  RNA       Date:  2001-09       Impact factor: 4.942

2.  Decapping and decay of messenger RNA occur in cytoplasmic processing bodies.

Authors:  Ujwal Sheth; Roy Parker
Journal:  Science       Date:  2003-05-02       Impact factor: 47.728

3.  Purifying mRNAs with a high-affinity eIF4E mutant identifies the short 3' poly(A) end phenotype.

Authors:  Youkyung Hwang Choi; Curt H Hagedorn
Journal:  Proc Natl Acad Sci U S A       Date:  2003-05-30       Impact factor: 11.205

4.  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

5.  Identification of a conserved interface between PUF and CPEB proteins.

Authors:  Zachary T Campbell; Elena Menichelli; Kyle Friend; Joann Wu; Judith Kimble; James R Williamson; Marvin Wickens
Journal:  J Biol Chem       Date:  2012-04-11       Impact factor: 5.157

6.  Patterns and plasticity in RNA-protein interactions enable recruitment of multiple proteins through a single site.

Authors:  Cary T Valley; Douglas F Porter; Chen Qiu; Zachary T Campbell; Traci M Tanaka Hall; Marvin Wickens
Journal:  Proc Natl Acad Sci U S A       Date:  2012-03-30       Impact factor: 11.205

7.  Predicting in vivo binding sites of RNA-binding proteins using mRNA secondary structure.

Authors:  Xiao Li; Gerald Quon; Howard D Lipshitz; Quaid Morris
Journal:  RNA       Date:  2010-04-23       Impact factor: 4.942

Review 8.  Mechanisms and consequences of subcellular RNA localization across diverse cell types.

Authors:  Krysta L Engel; Ankita Arora; Raeann Goering; Hei-Yong G Lo; J Matthew Taliaferro
Journal:  Traffic       Date:  2020-04-29       Impact factor: 6.215

9.  Codon optimality is a major determinant of mRNA stability.

Authors:  Vladimir Presnyak; Najwa Alhusaini; Ying-Hsin Chen; Sophie Martin; Nathan Morris; Nicholas Kline; Sara Olson; David Weinberg; Kristian E Baker; Brenton R Graveley; Jeff Coller
Journal:  Cell       Date:  2015-03-12       Impact factor: 41.582

Review 10.  Here, there, everywhere. mRNA localization in budding yeast.

Authors:  Birgit Singer-Krüger; Ralf-Peter Jansen
Journal:  RNA Biol       Date:  2014-10-31       Impact factor: 4.652

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