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Identifying eIF4E-binding protein translationally-controlled transcripts reveals links to mRNAs bound by specific PUF proteins

eIF4E-binding proteins (4E-BPs) regulate translation of mRNAs in eukaryotes. However the extent to which specific mRNA targets are regulated by 4E-BPs remains unknown. We performed translational profiling by microarray analysis of polysome and monosome associated mRNAs in wild-type and mutant cells...

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Autores principales: Cridge, Andrew G., Castelli, Lydia M., Smirnova, Julia B., Selley, Julian N., Rowe, William, Hubbard, Simon J., McCarthy, John E.G., Ashe, Mark P., Grant, Christopher M., Pavitt, Graham D.
Formato: Texto
Lenguaje:English
Publicado: Oxford University Press 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3001062/
https://www.ncbi.nlm.nih.gov/pubmed/20705650
http://dx.doi.org/10.1093/nar/gkq686
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author Cridge, Andrew G.
Castelli, Lydia M.
Smirnova, Julia B.
Selley, Julian N.
Rowe, William
Hubbard, Simon J.
McCarthy, John E.G.
Ashe, Mark P.
Grant, Christopher M.
Pavitt, Graham D.
author_facet Cridge, Andrew G.
Castelli, Lydia M.
Smirnova, Julia B.
Selley, Julian N.
Rowe, William
Hubbard, Simon J.
McCarthy, John E.G.
Ashe, Mark P.
Grant, Christopher M.
Pavitt, Graham D.
author_sort Cridge, Andrew G.
collection PubMed
description eIF4E-binding proteins (4E-BPs) regulate translation of mRNAs in eukaryotes. However the extent to which specific mRNA targets are regulated by 4E-BPs remains unknown. We performed translational profiling by microarray analysis of polysome and monosome associated mRNAs in wild-type and mutant cells to identify mRNAs in yeast regulated by the 4E-BPs Caf20p and Eap1p; the first-global comparison of 4E-BP target mRNAs. We find that yeast 4E-BPs modulate the translation of >1000 genes. Most target mRNAs differ between the 4E-BPs revealing mRNA specificity for translational control by each 4E-BP. This is supported by observations that eap1Δ and caf20Δ cells have different nitrogen source utilization defects, implying different mRNA targets. To account for the mRNA specificity shown by each 4E-BP, we found correlations between our data sets and previously determined targets of yeast mRNA-binding proteins. We used affinity chromatography experiments to uncover specific RNA-stabilized complexes formed between Caf20p and Puf4p/Puf5p and between Eap1p and Puf1p/Puf2p. Thus the combined action of each 4E-BP with specific 3′-UTR-binding proteins mediates mRNA-specific translational control in yeast, showing that this form of translational control is more widely employed than previously thought.
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spelling pubmed-30010622010-12-13 Identifying eIF4E-binding protein translationally-controlled transcripts reveals links to mRNAs bound by specific PUF proteins Cridge, Andrew G. Castelli, Lydia M. Smirnova, Julia B. Selley, Julian N. Rowe, William Hubbard, Simon J. McCarthy, John E.G. Ashe, Mark P. Grant, Christopher M. Pavitt, Graham D. Nucleic Acids Res Gene Regulation, Chromatin and Epigenetics eIF4E-binding proteins (4E-BPs) regulate translation of mRNAs in eukaryotes. However the extent to which specific mRNA targets are regulated by 4E-BPs remains unknown. We performed translational profiling by microarray analysis of polysome and monosome associated mRNAs in wild-type and mutant cells to identify mRNAs in yeast regulated by the 4E-BPs Caf20p and Eap1p; the first-global comparison of 4E-BP target mRNAs. We find that yeast 4E-BPs modulate the translation of >1000 genes. Most target mRNAs differ between the 4E-BPs revealing mRNA specificity for translational control by each 4E-BP. This is supported by observations that eap1Δ and caf20Δ cells have different nitrogen source utilization defects, implying different mRNA targets. To account for the mRNA specificity shown by each 4E-BP, we found correlations between our data sets and previously determined targets of yeast mRNA-binding proteins. We used affinity chromatography experiments to uncover specific RNA-stabilized complexes formed between Caf20p and Puf4p/Puf5p and between Eap1p and Puf1p/Puf2p. Thus the combined action of each 4E-BP with specific 3′-UTR-binding proteins mediates mRNA-specific translational control in yeast, showing that this form of translational control is more widely employed than previously thought. Oxford University Press 2010-12 2010-08-12 /pmc/articles/PMC3001062/ /pubmed/20705650 http://dx.doi.org/10.1093/nar/gkq686 Text en © The Author(s) 2010. Published by Oxford University Press. http://creativecommons.org/licenses/by-nc/2.5 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/2.5), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Gene Regulation, Chromatin and Epigenetics
Cridge, Andrew G.
Castelli, Lydia M.
Smirnova, Julia B.
Selley, Julian N.
Rowe, William
Hubbard, Simon J.
McCarthy, John E.G.
Ashe, Mark P.
Grant, Christopher M.
Pavitt, Graham D.
Identifying eIF4E-binding protein translationally-controlled transcripts reveals links to mRNAs bound by specific PUF proteins
title Identifying eIF4E-binding protein translationally-controlled transcripts reveals links to mRNAs bound by specific PUF proteins
title_full Identifying eIF4E-binding protein translationally-controlled transcripts reveals links to mRNAs bound by specific PUF proteins
title_fullStr Identifying eIF4E-binding protein translationally-controlled transcripts reveals links to mRNAs bound by specific PUF proteins
title_full_unstemmed Identifying eIF4E-binding protein translationally-controlled transcripts reveals links to mRNAs bound by specific PUF proteins
title_short Identifying eIF4E-binding protein translationally-controlled transcripts reveals links to mRNAs bound by specific PUF proteins
title_sort identifying eif4e-binding protein translationally-controlled transcripts reveals links to mrnas bound by specific puf proteins
topic Gene Regulation, Chromatin and Epigenetics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3001062/
https://www.ncbi.nlm.nih.gov/pubmed/20705650
http://dx.doi.org/10.1093/nar/gkq686
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