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Deficiency in mTORC1-controlled C/EBPβ-mRNA translation improves metabolic health in mice

The mammalian target of rapamycin complex 1 (mTORC1) is a central regulator of physiological adaptations in response to changes in nutrient supply. Major downstream targets of mTORC1 signalling are the mRNA translation regulators p70 ribosomal protein S6 kinase 1 (S6K1p70) and the 4E-binding protein...

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Autores principales: Zidek, Laura M, Ackermann, Tobias, Hartleben, Götz, Eichwald, Sabrina, Kortman, Gertrud, Kiehntopf, Michael, Leutz, Achim, Sonenberg, Nahum, Wang, Zhao-Qi, von Maltzahn, Julia, Müller, Christine, Calkhoven, Cornelis F
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Ltd 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4552494/
https://www.ncbi.nlm.nih.gov/pubmed/26113365
http://dx.doi.org/10.15252/embr.201439837
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author Zidek, Laura M
Ackermann, Tobias
Hartleben, Götz
Eichwald, Sabrina
Kortman, Gertrud
Kiehntopf, Michael
Leutz, Achim
Sonenberg, Nahum
Wang, Zhao-Qi
von Maltzahn, Julia
Müller, Christine
Calkhoven, Cornelis F
author_facet Zidek, Laura M
Ackermann, Tobias
Hartleben, Götz
Eichwald, Sabrina
Kortman, Gertrud
Kiehntopf, Michael
Leutz, Achim
Sonenberg, Nahum
Wang, Zhao-Qi
von Maltzahn, Julia
Müller, Christine
Calkhoven, Cornelis F
author_sort Zidek, Laura M
collection PubMed
description The mammalian target of rapamycin complex 1 (mTORC1) is a central regulator of physiological adaptations in response to changes in nutrient supply. Major downstream targets of mTORC1 signalling are the mRNA translation regulators p70 ribosomal protein S6 kinase 1 (S6K1p70) and the 4E-binding proteins (4E-BPs). However, little is known about vertebrate mRNAs that are specifically controlled by mTORC1 signalling and are engaged in regulating mTORC1-associated physiology. Here, we show that translation of the CCAAT/enhancer binding protein beta (C/EBPβ) mRNA into the C/EBPβ-LIP isoform is suppressed in response to mTORC1 inhibition either through pharmacological treatment or through calorie restriction. Our data indicate that the function of 4E-BPs is required for suppression of LIP. Intriguingly, mice lacking the cis-regulatory upstream open reading frame (uORF) in the C/EBPβ-mRNA, which is required for mTORC1-stimulated translation into C/EBPβ-LIP, display an improved metabolic phenotype with features also found under calorie restriction. Thus, our data suggest that translational adjustment of C/EBPβ-isoform expression is one of the key processes that direct metabolic adaptation in response to changes in mTORC1 activity.
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spelling pubmed-45524942015-12-04 Deficiency in mTORC1-controlled C/EBPβ-mRNA translation improves metabolic health in mice Zidek, Laura M Ackermann, Tobias Hartleben, Götz Eichwald, Sabrina Kortman, Gertrud Kiehntopf, Michael Leutz, Achim Sonenberg, Nahum Wang, Zhao-Qi von Maltzahn, Julia Müller, Christine Calkhoven, Cornelis F EMBO Rep Articles The mammalian target of rapamycin complex 1 (mTORC1) is a central regulator of physiological adaptations in response to changes in nutrient supply. Major downstream targets of mTORC1 signalling are the mRNA translation regulators p70 ribosomal protein S6 kinase 1 (S6K1p70) and the 4E-binding proteins (4E-BPs). However, little is known about vertebrate mRNAs that are specifically controlled by mTORC1 signalling and are engaged in regulating mTORC1-associated physiology. Here, we show that translation of the CCAAT/enhancer binding protein beta (C/EBPβ) mRNA into the C/EBPβ-LIP isoform is suppressed in response to mTORC1 inhibition either through pharmacological treatment or through calorie restriction. Our data indicate that the function of 4E-BPs is required for suppression of LIP. Intriguingly, mice lacking the cis-regulatory upstream open reading frame (uORF) in the C/EBPβ-mRNA, which is required for mTORC1-stimulated translation into C/EBPβ-LIP, display an improved metabolic phenotype with features also found under calorie restriction. Thus, our data suggest that translational adjustment of C/EBPβ-isoform expression is one of the key processes that direct metabolic adaptation in response to changes in mTORC1 activity. John Wiley & Sons, Ltd 2015-08 2015-06-25 /pmc/articles/PMC4552494/ /pubmed/26113365 http://dx.doi.org/10.15252/embr.201439837 Text en © 2015 The Authors. Published under the terms of the CC BY NC ND 4.0 license http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.
spellingShingle Articles
Zidek, Laura M
Ackermann, Tobias
Hartleben, Götz
Eichwald, Sabrina
Kortman, Gertrud
Kiehntopf, Michael
Leutz, Achim
Sonenberg, Nahum
Wang, Zhao-Qi
von Maltzahn, Julia
Müller, Christine
Calkhoven, Cornelis F
Deficiency in mTORC1-controlled C/EBPβ-mRNA translation improves metabolic health in mice
title Deficiency in mTORC1-controlled C/EBPβ-mRNA translation improves metabolic health in mice
title_full Deficiency in mTORC1-controlled C/EBPβ-mRNA translation improves metabolic health in mice
title_fullStr Deficiency in mTORC1-controlled C/EBPβ-mRNA translation improves metabolic health in mice
title_full_unstemmed Deficiency in mTORC1-controlled C/EBPβ-mRNA translation improves metabolic health in mice
title_short Deficiency in mTORC1-controlled C/EBPβ-mRNA translation improves metabolic health in mice
title_sort deficiency in mtorc1-controlled c/ebpβ-mrna translation improves metabolic health in mice
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4552494/
https://www.ncbi.nlm.nih.gov/pubmed/26113365
http://dx.doi.org/10.15252/embr.201439837
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