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Dynamic Metabolite Profiling in an Archaeon Connects Transcriptional Regulation to Metabolic Consequences

Previous work demonstrated that the TrmB transcription factor is responsible for regulating the expression of many enzyme-coding genes in the hypersaline-adapted archaeon Halobacterium salinarum via a direct interaction with a cis-regulatory sequence in their promoters. This interaction is abolished...

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Autores principales: Todor, Horia, Gooding, Jessica, Ilkayeva, Olga R., Schmid, Amy K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4540570/
https://www.ncbi.nlm.nih.gov/pubmed/26284786
http://dx.doi.org/10.1371/journal.pone.0135693
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author Todor, Horia
Gooding, Jessica
Ilkayeva, Olga R.
Schmid, Amy K.
author_facet Todor, Horia
Gooding, Jessica
Ilkayeva, Olga R.
Schmid, Amy K.
author_sort Todor, Horia
collection PubMed
description Previous work demonstrated that the TrmB transcription factor is responsible for regulating the expression of many enzyme-coding genes in the hypersaline-adapted archaeon Halobacterium salinarum via a direct interaction with a cis-regulatory sequence in their promoters. This interaction is abolished in the presence of glucose. Although much is known about the effects of TrmB at the transcriptional level, it remains unclear whether and to what extent changes in mRNA levels directly affect metabolite levels. In order to address this question, here we performed a high-resolution metabolite profiling time course during a change in nutrients using a combination of targeted and untargeted methods in wild-type and ΔtrmB strain backgrounds. We found that TrmB-mediated transcriptional changes resulted in widespread and significant changes to metabolite levels across the metabolic network. Additionally, the pattern of growth complementation using various purines suggests that the mis-regulation of gluconeogenesis in the ΔtrmB mutant strain in the absence of glucose results in low phosphoribosylpyrophosphate (PRPP) levels. We confirmed these low PRPP levels using a quantitative mass spectrometric technique and found that they are associated with a metabolic block in de novo purine synthesis, which is partially responsible for the growth defect of the ΔtrmB mutant strain in the absence of glucose. In conclusion, we show how transcriptional regulation of metabolism affects metabolite levels and ultimately, phenotypes.
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spelling pubmed-45405702015-08-24 Dynamic Metabolite Profiling in an Archaeon Connects Transcriptional Regulation to Metabolic Consequences Todor, Horia Gooding, Jessica Ilkayeva, Olga R. Schmid, Amy K. PLoS One Research Article Previous work demonstrated that the TrmB transcription factor is responsible for regulating the expression of many enzyme-coding genes in the hypersaline-adapted archaeon Halobacterium salinarum via a direct interaction with a cis-regulatory sequence in their promoters. This interaction is abolished in the presence of glucose. Although much is known about the effects of TrmB at the transcriptional level, it remains unclear whether and to what extent changes in mRNA levels directly affect metabolite levels. In order to address this question, here we performed a high-resolution metabolite profiling time course during a change in nutrients using a combination of targeted and untargeted methods in wild-type and ΔtrmB strain backgrounds. We found that TrmB-mediated transcriptional changes resulted in widespread and significant changes to metabolite levels across the metabolic network. Additionally, the pattern of growth complementation using various purines suggests that the mis-regulation of gluconeogenesis in the ΔtrmB mutant strain in the absence of glucose results in low phosphoribosylpyrophosphate (PRPP) levels. We confirmed these low PRPP levels using a quantitative mass spectrometric technique and found that they are associated with a metabolic block in de novo purine synthesis, which is partially responsible for the growth defect of the ΔtrmB mutant strain in the absence of glucose. In conclusion, we show how transcriptional regulation of metabolism affects metabolite levels and ultimately, phenotypes. Public Library of Science 2015-08-18 /pmc/articles/PMC4540570/ /pubmed/26284786 http://dx.doi.org/10.1371/journal.pone.0135693 Text en © 2015 Todor et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Todor, Horia
Gooding, Jessica
Ilkayeva, Olga R.
Schmid, Amy K.
Dynamic Metabolite Profiling in an Archaeon Connects Transcriptional Regulation to Metabolic Consequences
title Dynamic Metabolite Profiling in an Archaeon Connects Transcriptional Regulation to Metabolic Consequences
title_full Dynamic Metabolite Profiling in an Archaeon Connects Transcriptional Regulation to Metabolic Consequences
title_fullStr Dynamic Metabolite Profiling in an Archaeon Connects Transcriptional Regulation to Metabolic Consequences
title_full_unstemmed Dynamic Metabolite Profiling in an Archaeon Connects Transcriptional Regulation to Metabolic Consequences
title_short Dynamic Metabolite Profiling in an Archaeon Connects Transcriptional Regulation to Metabolic Consequences
title_sort dynamic metabolite profiling in an archaeon connects transcriptional regulation to metabolic consequences
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4540570/
https://www.ncbi.nlm.nih.gov/pubmed/26284786
http://dx.doi.org/10.1371/journal.pone.0135693
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