Literature DB >> 14685270

Drosophila Cup is an eIF4E-binding protein that functions in Smaug-mediated translational repression.

Meryl R Nelson1, Andrew M Leidal, Craig A Smibert.   

Abstract

Translational regulation plays an essential role in development and often involves factors that interact with sequences in the 3' untranslated region (UTR) of specific mRNAs. For example, Nanos protein at the posterior of the Drosophila embryo directs posterior development, and this localization requires selective translation of posteriorly localized nanos mRNA. Spatial regulation of nanos translation requires Smaug protein bound to the nanos 3' UTR, which represses the translation of unlocalized nanos transcripts. While the function of 3' UTR-bound translational regulators is, in general, poorly understood, they presumably interact with the basic translation machinery. Here we demonstrate that Smaug interacts with the Cup protein and that Cup is an eIF4E-binding protein that blocks the binding of eIF4G to eIF4E. Cup mediates an indirect interaction between Smaug and eIF4E, and Smaug function in vivo requires Cup. Thus, Smaug represses translation via a Cup-dependent block in eIF4G recruitment.

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Year:  2003        PMID: 14685270      PMCID: PMC1271664          DOI: 10.1038/sj.emboj.7600026

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


  45 in total

1.  Cap-dependent translation initiation in eukaryotes is regulated by a molecular mimic of eIF4G.

Authors:  J Marcotrigiano; A C Gingras; N Sonenberg; S K Burley
Journal:  Mol Cell       Date:  1999-06       Impact factor: 17.970

2.  Synthesis of the posterior determinant Nanos is spatially restricted by a novel cotranslational regulatory mechanism.

Authors:  I E Clark; D Wyckoff; E R Gavis
Journal:  Curr Biol       Date:  2000-10-19       Impact factor: 10.834

3.  Overlapping but distinct RNA elements control repression and activation of nanos translation.

Authors:  S Crucs; S Chatterjee; E R Gavis
Journal:  Mol Cell       Date:  2000-03       Impact factor: 17.970

4.  Maskin is a CPEB-associated factor that transiently interacts with elF-4E.

Authors:  B Stebbins-Boaz; Q Cao; C H de Moor; R Mendez; J D Richter
Journal:  Mol Cell       Date:  1999-12       Impact factor: 17.970

Review 5.  eIF4 initiation factors: effectors of mRNA recruitment to ribosomes and regulators of translation.

Authors:  A C Gingras; B Raught; N Sonenberg
Journal:  Annu Rev Biochem       Date:  1999       Impact factor: 23.643

6.  A novel shuttling protein, 4E-T, mediates the nuclear import of the mRNA 5' cap-binding protein, eIF4E.

Authors:  J Dostie; M Ferraiuolo; A Pause; S A Adam; N Sonenberg
Journal:  EMBO J       Date:  2000-06-15       Impact factor: 11.598

7.  Poly(A)-independent regulation of maternal hunchback translation in the Drosophila embryo.

Authors:  D Chagnovich; R Lehmann
Journal:  Proc Natl Acad Sci U S A       Date:  2001-09-18       Impact factor: 11.205

8.  Smaug, a novel RNA-binding protein that operates a translational switch in Drosophila.

Authors:  A Dahanukar; J A Walker; R P Wharton
Journal:  Mol Cell       Date:  1999-08       Impact factor: 17.970

9.  Smaug, a novel and conserved protein, contributes to repression of nanos mRNA translation in vitro.

Authors:  C A Smibert; Y S Lie; W Shillinglaw; W J Henzel; P M Macdonald
Journal:  RNA       Date:  1999-12       Impact factor: 4.942

10.  Nanos interacts with cup in the female germline of Drosophila.

Authors:  A C Verrotti; R P Wharton
Journal:  Development       Date:  2000-12       Impact factor: 6.868

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  94 in total

Review 1.  New insights into the regulation of RNP granule assembly in oocytes.

Authors:  Jennifer A Schisa
Journal:  Int Rev Cell Mol Biol       Date:  2012       Impact factor: 6.813

2.  From cis-regulatory elements to complex RNPs and back.

Authors:  Fátima Gebauer; Thomas Preiss; Matthias W Hentze
Journal:  Cold Spring Harb Perspect Biol       Date:  2012-07-01       Impact factor: 10.005

3.  Smaug assembles an ATP-dependent stable complex repressing nanos mRNA translation at multiple levels.

Authors:  Mandy Jeske; Bodo Moritz; Alexander Anders; Elmar Wahle
Journal:  EMBO J       Date:  2010-11-16       Impact factor: 11.598

4.  Subunits of the Drosophila CCR4-NOT complex and their roles in mRNA deadenylation.

Authors:  Claudia Temme; Lianbing Zhang; Elisabeth Kremmer; Christian Ihling; Aymeric Chartier; Andrea Sinz; Martine Simonelig; Elmar Wahle
Journal:  RNA       Date:  2010-05-26       Impact factor: 4.942

Review 5.  Germ Line Versus Soma in the Transition from Egg to Embryo.

Authors:  S Zachary Swartz; Gary M Wessel
Journal:  Curr Top Dev Biol       Date:  2015-08-19       Impact factor: 4.897

Review 6.  Regulation of translation initiation in eukaryotes: mechanisms and biological targets.

Authors:  Nahum Sonenberg; Alan G Hinnebusch
Journal:  Cell       Date:  2009-02-20       Impact factor: 41.582

Review 7.  eIF4E: new family members, new binding partners, new roles.

Authors:  Robert E Rhoads
Journal:  J Biol Chem       Date:  2009-02-23       Impact factor: 5.157

8.  Differential phosphorylation controls Maskin association with eukaryotic translation initiation factor 4E and localization on the mitotic apparatus.

Authors:  Daron C Barnard; Quiping Cao; Joel D Richter
Journal:  Mol Cell Biol       Date:  2005-09       Impact factor: 4.272

9.  Vasa promotes Drosophila germline stem cell differentiation by activating mei-P26 translation by directly interacting with a (U)-rich motif in its 3' UTR.

Authors:  Niankun Liu; Hong Han; Paul Lasko
Journal:  Genes Dev       Date:  2009-12-01       Impact factor: 11.361

10.  Emx2 homeodomain transcription factor interacts with eukaryotic translation initiation factor 4E (eIF4E) in the axons of olfactory sensory neurons.

Authors:  Stéphane Nédélec; Isabelle Foucher; Isabelle Brunet; Colette Bouillot; Alain Prochiantz; Alain Trembleau
Journal:  Proc Natl Acad Sci U S A       Date:  2004-07-09       Impact factor: 11.205

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