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CspC regulates the expression of the glyoxylate cycle genes at stationary phase in Caulobacter

BACKGROUND: The Cold Shock proteins are RNA binding proteins involved in various cellular processes, including adaptation to low temperature, nutritional stress, cell growth and stationary phase. They may have an impact on gene expression by interfering with RNA stability and acting as transcription...

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Autores principales: Santos, Juliana S., da Silva, Carolina A. P. T., Balhesteros, Heloise, Lourenço, Rogério F., Marques, Marilis V.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4551563/
https://www.ncbi.nlm.nih.gov/pubmed/26311251
http://dx.doi.org/10.1186/s12864-015-1845-1
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author Santos, Juliana S.
da Silva, Carolina A. P. T.
Balhesteros, Heloise
Lourenço, Rogério F.
Marques, Marilis V.
author_facet Santos, Juliana S.
da Silva, Carolina A. P. T.
Balhesteros, Heloise
Lourenço, Rogério F.
Marques, Marilis V.
author_sort Santos, Juliana S.
collection PubMed
description BACKGROUND: The Cold Shock proteins are RNA binding proteins involved in various cellular processes, including adaptation to low temperature, nutritional stress, cell growth and stationary phase. They may have an impact on gene expression by interfering with RNA stability and acting as transcription antiterminators. Caulobacter crescentus cspC is an essential gene encoding a stationary phase-induced protein of the Cold Shock Protein family and this work had as goal investigating the basis for the requirement of this gene for survival at this phase. In this work we investigate the role of CspC in C. crescentus stationary phase and discuss the molecular mechanisms that could be involved. RESULTS: The expression of cspC increased significantly at stationary phase in complex media and in glucose depletion, indicating a putative role in responding to carbon starvation. Global transcriptional profiling experiments comparing cspC and the wild type strain both at exponential and stationary phases as well as comparing exponential and stationary phase in wild type strain were carried out by DNA microarray analysis. The results showed that the absence of cspC affected the transcription of 11 genes at exponential phase and 60 genes at stationary phase. Among the differentially expressed genes it is worth noting those encoding respiratory enzymes and genes for sulfur metabolism, which were upregulated, and those encoding enzymes of the glyoxylate cycle, which were severely downregulated in the mutant at stationary phase. mRNA decay experiments showed that the aceA mRNA, encoding isocitrate lyase, was less stable in the cspC mutant, indicating that this effect was at least partially due to posttranscriptional regulation. These observations were supported by the observed arrested growth phenotype of the cspC strain when grown in acetate as the sole carbon source, and by the upregulation of genes for assimilatory sulfate reduction and methionine biosynthesis. CONCLUSIONS: The stationary phase-induced RNA binding protein CspC has an important role in gene expression at this phase, and is necessary for maximal expression of the glyoxylate cycle genes. In the case of aceA, its downregulation may be attributed to the shorter half-life of the mRNA in the cspC mutant, indicating that one of the possible regulatory mechanisms is via altering RNA stabilization. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12864-015-1845-1) contains supplementary material, which is available to authorized users.
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spelling pubmed-45515632015-08-29 CspC regulates the expression of the glyoxylate cycle genes at stationary phase in Caulobacter Santos, Juliana S. da Silva, Carolina A. P. T. Balhesteros, Heloise Lourenço, Rogério F. Marques, Marilis V. BMC Genomics Research Article BACKGROUND: The Cold Shock proteins are RNA binding proteins involved in various cellular processes, including adaptation to low temperature, nutritional stress, cell growth and stationary phase. They may have an impact on gene expression by interfering with RNA stability and acting as transcription antiterminators. Caulobacter crescentus cspC is an essential gene encoding a stationary phase-induced protein of the Cold Shock Protein family and this work had as goal investigating the basis for the requirement of this gene for survival at this phase. In this work we investigate the role of CspC in C. crescentus stationary phase and discuss the molecular mechanisms that could be involved. RESULTS: The expression of cspC increased significantly at stationary phase in complex media and in glucose depletion, indicating a putative role in responding to carbon starvation. Global transcriptional profiling experiments comparing cspC and the wild type strain both at exponential and stationary phases as well as comparing exponential and stationary phase in wild type strain were carried out by DNA microarray analysis. The results showed that the absence of cspC affected the transcription of 11 genes at exponential phase and 60 genes at stationary phase. Among the differentially expressed genes it is worth noting those encoding respiratory enzymes and genes for sulfur metabolism, which were upregulated, and those encoding enzymes of the glyoxylate cycle, which were severely downregulated in the mutant at stationary phase. mRNA decay experiments showed that the aceA mRNA, encoding isocitrate lyase, was less stable in the cspC mutant, indicating that this effect was at least partially due to posttranscriptional regulation. These observations were supported by the observed arrested growth phenotype of the cspC strain when grown in acetate as the sole carbon source, and by the upregulation of genes for assimilatory sulfate reduction and methionine biosynthesis. CONCLUSIONS: The stationary phase-induced RNA binding protein CspC has an important role in gene expression at this phase, and is necessary for maximal expression of the glyoxylate cycle genes. In the case of aceA, its downregulation may be attributed to the shorter half-life of the mRNA in the cspC mutant, indicating that one of the possible regulatory mechanisms is via altering RNA stabilization. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12864-015-1845-1) contains supplementary material, which is available to authorized users. BioMed Central 2015-08-27 /pmc/articles/PMC4551563/ /pubmed/26311251 http://dx.doi.org/10.1186/s12864-015-1845-1 Text en © Santos et al. 2015 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Santos, Juliana S.
da Silva, Carolina A. P. T.
Balhesteros, Heloise
Lourenço, Rogério F.
Marques, Marilis V.
CspC regulates the expression of the glyoxylate cycle genes at stationary phase in Caulobacter
title CspC regulates the expression of the glyoxylate cycle genes at stationary phase in Caulobacter
title_full CspC regulates the expression of the glyoxylate cycle genes at stationary phase in Caulobacter
title_fullStr CspC regulates the expression of the glyoxylate cycle genes at stationary phase in Caulobacter
title_full_unstemmed CspC regulates the expression of the glyoxylate cycle genes at stationary phase in Caulobacter
title_short CspC regulates the expression of the glyoxylate cycle genes at stationary phase in Caulobacter
title_sort cspc regulates the expression of the glyoxylate cycle genes at stationary phase in caulobacter
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4551563/
https://www.ncbi.nlm.nih.gov/pubmed/26311251
http://dx.doi.org/10.1186/s12864-015-1845-1
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