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Dynamic changes in eIF4F-mRNA interactions revealed by global analyses of environmental stress responses.
Costello, Joseph L; Kershaw, Christopher J; Castelli, Lydia M; Talavera, David; Rowe, William; Sims, Paul F G; Ashe, Mark P; Grant, Christopher M; Hubbard, Simon J; Pavitt, Graham D.
Affiliation
  • Costello JL; Division of Molecular and Cellular Function, School of Biological Sciences, Faculty of Biology Medicine and Health, Manchester Academic Health Science Centre, The University of Manchester, Manchester, M13 9PT, UK.
  • Kershaw CJ; Present address: Biosciences, College of Life and Environmental Sciences, Geoffrey Pope Building, University of Exeter, Stocker Road, Exeter, EX4 4QD, UK.
  • Castelli LM; Division of Molecular and Cellular Function, School of Biological Sciences, Faculty of Biology Medicine and Health, Manchester Academic Health Science Centre, The University of Manchester, Manchester, M13 9PT, UK.
  • Talavera D; Division of Molecular and Cellular Function, School of Biological Sciences, Faculty of Biology Medicine and Health, Manchester Academic Health Science Centre, The University of Manchester, Manchester, M13 9PT, UK.
  • Rowe W; Present address: Sheffield Institute for Translational Neuroscience, The University of Sheffield, 385a Glossop Road, Sheffield, S10 2HQ, UK.
  • Sims PFG; Division of Cardiovascular Sciences, School of Medicine, Faculty of Biology Medicine and Health, Manchester Academic Health Science Centre, The University of Manchester, Manchester, M13 9PT, UK.
  • Ashe MP; Division of Molecular and Cellular Function, School of Biological Sciences, Faculty of Biology Medicine and Health, Manchester Academic Health Science Centre, The University of Manchester, Manchester, M13 9PT, UK.
  • Grant CM; Present address: Department of Chemistry, Loughborough University, Epinal Way, Loughborough, Leicestershire, LE11 3TU, UK.
  • Hubbard SJ; Manchester Institute of Biotechnology (MIB), The University of Manchester, 131 Princess Street, Manchester, M1 7DN, UK.
  • Pavitt GD; Division of Molecular and Cellular Function, School of Biological Sciences, Faculty of Biology Medicine and Health, Manchester Academic Health Science Centre, The University of Manchester, Manchester, M13 9PT, UK.
Genome Biol ; 18(1): 201, 2017 10 27.
Article de En | MEDLINE | ID: mdl-29078784
ABSTRACT

BACKGROUND:

Translation factors eIF4E and eIF4G form eIF4F, which interacts with the messenger RNA (mRNA) 5' cap to promote ribosome recruitment and translation initiation. Variations in the association of eIF4F with individual mRNAs likely contribute to differences in translation initiation frequencies between mRNAs. As translation initiation is globally reprogrammed by environmental stresses, we were interested in determining whether eIF4F interactions with individual mRNAs are reprogrammed and how this may contribute to global environmental stress responses.

RESULTS:

Using a tagged-factor protein capture and RNA-sequencing (RNA-seq) approach, we have assessed how mRNA associations with eIF4E, eIF4G1 and eIF4G2 change globally in response to three defined stresses that each cause a rapid attenuation of protein

synthesis:

oxidative stress induced by hydrogen peroxide and nutrient stresses caused by amino acid or glucose withdrawal. We find that acute stress leads to dynamic and unexpected changes in eIF4F-mRNA interactions that are shared among each factor and across the stresses imposed. eIF4F-mRNA interactions stabilised by stress are predominantly associated with translational repression, while more actively initiating mRNAs become relatively depleted for eIF4F. Simultaneously, other mRNAs are insulated from these stress-induced changes in eIF4F association.

CONCLUSION:

Dynamic eIF4F-mRNA interaction changes are part of a coordinated early translational control response shared across environmental stresses. Our data are compatible with a model where multiple mRNA closed-loop complexes form with differing stability. Hence, unexpectedly, in the absence of other stabilising factors, rapid translation initiation on mRNAs correlates with less stable eIF4F interactions.
Sujet(s)
Mots clés

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Initiation de la traduction / Stress physiologique / ARN messager / Facteur-4F d'initiation eucaryote Type d'étude: Prognostic_studies Langue: En Journal: Genome Biol Sujet du journal: BIOLOGIA MOLECULAR / GENETICA Année: 2017 Type de document: Article Pays d'affiliation: Royaume-Uni

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Initiation de la traduction / Stress physiologique / ARN messager / Facteur-4F d'initiation eucaryote Type d'étude: Prognostic_studies Langue: En Journal: Genome Biol Sujet du journal: BIOLOGIA MOLECULAR / GENETICA Année: 2017 Type de document: Article Pays d'affiliation: Royaume-Uni
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