Cargando…

Optimization of carbon and energy utilization through differential translational efficiency

Control of translation is vital to all species. Here we employ a multi-omics approach to decipher condition-dependent translational regulation in the model acetogen Clostridium ljungdahlii. Integration of data from cells grown autotrophically or heterotrophically revealed that pathways critical to c...

Descripción completa

Detalles Bibliográficos
Autores principales: Al-Bassam, Mahmoud M., Kim, Ji-Nu, Zaramela, Livia S., Kellman, Benjamin P., Zuniga, Cristal, Wozniak, Jacob M., Gonzalez, David J., Zengler, Karsten
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6203783/
https://www.ncbi.nlm.nih.gov/pubmed/30367068
http://dx.doi.org/10.1038/s41467-018-06993-6
_version_ 1783365932584796160
author Al-Bassam, Mahmoud M.
Kim, Ji-Nu
Zaramela, Livia S.
Kellman, Benjamin P.
Zuniga, Cristal
Wozniak, Jacob M.
Gonzalez, David J.
Zengler, Karsten
author_facet Al-Bassam, Mahmoud M.
Kim, Ji-Nu
Zaramela, Livia S.
Kellman, Benjamin P.
Zuniga, Cristal
Wozniak, Jacob M.
Gonzalez, David J.
Zengler, Karsten
author_sort Al-Bassam, Mahmoud M.
collection PubMed
description Control of translation is vital to all species. Here we employ a multi-omics approach to decipher condition-dependent translational regulation in the model acetogen Clostridium ljungdahlii. Integration of data from cells grown autotrophically or heterotrophically revealed that pathways critical to carbon and energy metabolism are under strong translational regulation. Major pathways involved in carbon and energy metabolism are not only differentially transcribed and translated, but their translational efficiencies are differentially elevated in response to resource availability under different growth conditions. We show that translational efficiency is not static and that it changes dynamically in response to mRNA expression levels. mRNAs harboring optimized 5′-untranslated region and coding region features, have higher translational efficiencies and are significantly enriched in genes encoding carbon and energy metabolism. In contrast, mRNAs enriched in housekeeping functions harbor sub-optimal features and have lower translational efficiencies. We propose that regulation of translational efficiency is crucial for effectively controlling resource allocation in energy-deprived microorganisms.
format Online
Article
Text
id pubmed-6203783
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-62037832018-10-29 Optimization of carbon and energy utilization through differential translational efficiency Al-Bassam, Mahmoud M. Kim, Ji-Nu Zaramela, Livia S. Kellman, Benjamin P. Zuniga, Cristal Wozniak, Jacob M. Gonzalez, David J. Zengler, Karsten Nat Commun Article Control of translation is vital to all species. Here we employ a multi-omics approach to decipher condition-dependent translational regulation in the model acetogen Clostridium ljungdahlii. Integration of data from cells grown autotrophically or heterotrophically revealed that pathways critical to carbon and energy metabolism are under strong translational regulation. Major pathways involved in carbon and energy metabolism are not only differentially transcribed and translated, but their translational efficiencies are differentially elevated in response to resource availability under different growth conditions. We show that translational efficiency is not static and that it changes dynamically in response to mRNA expression levels. mRNAs harboring optimized 5′-untranslated region and coding region features, have higher translational efficiencies and are significantly enriched in genes encoding carbon and energy metabolism. In contrast, mRNAs enriched in housekeeping functions harbor sub-optimal features and have lower translational efficiencies. We propose that regulation of translational efficiency is crucial for effectively controlling resource allocation in energy-deprived microorganisms. Nature Publishing Group UK 2018-10-26 /pmc/articles/PMC6203783/ /pubmed/30367068 http://dx.doi.org/10.1038/s41467-018-06993-6 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Al-Bassam, Mahmoud M.
Kim, Ji-Nu
Zaramela, Livia S.
Kellman, Benjamin P.
Zuniga, Cristal
Wozniak, Jacob M.
Gonzalez, David J.
Zengler, Karsten
Optimization of carbon and energy utilization through differential translational efficiency
title Optimization of carbon and energy utilization through differential translational efficiency
title_full Optimization of carbon and energy utilization through differential translational efficiency
title_fullStr Optimization of carbon and energy utilization through differential translational efficiency
title_full_unstemmed Optimization of carbon and energy utilization through differential translational efficiency
title_short Optimization of carbon and energy utilization through differential translational efficiency
title_sort optimization of carbon and energy utilization through differential translational efficiency
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6203783/
https://www.ncbi.nlm.nih.gov/pubmed/30367068
http://dx.doi.org/10.1038/s41467-018-06993-6
work_keys_str_mv AT albassammahmoudm optimizationofcarbonandenergyutilizationthroughdifferentialtranslationalefficiency
AT kimjinu optimizationofcarbonandenergyutilizationthroughdifferentialtranslationalefficiency
AT zaramelalivias optimizationofcarbonandenergyutilizationthroughdifferentialtranslationalefficiency
AT kellmanbenjaminp optimizationofcarbonandenergyutilizationthroughdifferentialtranslationalefficiency
AT zunigacristal optimizationofcarbonandenergyutilizationthroughdifferentialtranslationalefficiency
AT wozniakjacobm optimizationofcarbonandenergyutilizationthroughdifferentialtranslationalefficiency
AT gonzalezdavidj optimizationofcarbonandenergyutilizationthroughdifferentialtranslationalefficiency
AT zenglerkarsten optimizationofcarbonandenergyutilizationthroughdifferentialtranslationalefficiency