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Transcriptional and post-transcriptional events trigger de novo infB expression in cold stressed Escherichia coli

After a 37 to 10°C temperature downshift the level of translation initiation factor IF2, like that of IF1 and IF3, increases at least 3-fold with respect to the ribosomes. To clarify the mechanisms and conditions leading to cold-stress induction of infB expression, the consequences of this temperatu...

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Autores principales: Brandi, Anna, Giangrossi, Mara, Paoloni, Silvia, Spurio, Roberto, Giuliodori, Anna M, Pon, Cynthia L, Gualerzi, Claudio O
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6511841/
https://www.ncbi.nlm.nih.gov/pubmed/30916329
http://dx.doi.org/10.1093/nar/gkz187
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author Brandi, Anna
Giangrossi, Mara
Paoloni, Silvia
Spurio, Roberto
Giuliodori, Anna M
Pon, Cynthia L
Gualerzi, Claudio O
author_facet Brandi, Anna
Giangrossi, Mara
Paoloni, Silvia
Spurio, Roberto
Giuliodori, Anna M
Pon, Cynthia L
Gualerzi, Claudio O
author_sort Brandi, Anna
collection PubMed
description After a 37 to 10°C temperature downshift the level of translation initiation factor IF2, like that of IF1 and IF3, increases at least 3-fold with respect to the ribosomes. To clarify the mechanisms and conditions leading to cold-stress induction of infB expression, the consequences of this temperature shift on infB (IF2) transcription, infB mRNA stability and translation were analysed. The Escherichia coli gene encoding IF2 is part of the metY-nusA-infB operon that contains three known promoters (P-1, P0 and P2) in addition to two promoters P3 and P4 identified in this study, the latter committed to the synthesis of a monocistronic mRNA encoding exclusively IF2. The results obtained indicate that the increased level of IF2 following cold stress depends on three mechanisms: (i) activation of all the promoters of the operon, P-1 being the most cold-responsive, as a likely consequence of the reduction of the ppGpp level that follows cold stress; (ii) a large increase in infB mRNA half-life and (iii) the cold-shock induced translational bias that ensures efficient translation of infB mRNA by the translational apparatus of cold shocked cells. A comparison of the mechanisms responsible for the cold shock induction of the three initiation factors is also presented.
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spelling pubmed-65118412019-05-20 Transcriptional and post-transcriptional events trigger de novo infB expression in cold stressed Escherichia coli Brandi, Anna Giangrossi, Mara Paoloni, Silvia Spurio, Roberto Giuliodori, Anna M Pon, Cynthia L Gualerzi, Claudio O Nucleic Acids Res Molecular Biology After a 37 to 10°C temperature downshift the level of translation initiation factor IF2, like that of IF1 and IF3, increases at least 3-fold with respect to the ribosomes. To clarify the mechanisms and conditions leading to cold-stress induction of infB expression, the consequences of this temperature shift on infB (IF2) transcription, infB mRNA stability and translation were analysed. The Escherichia coli gene encoding IF2 is part of the metY-nusA-infB operon that contains three known promoters (P-1, P0 and P2) in addition to two promoters P3 and P4 identified in this study, the latter committed to the synthesis of a monocistronic mRNA encoding exclusively IF2. The results obtained indicate that the increased level of IF2 following cold stress depends on three mechanisms: (i) activation of all the promoters of the operon, P-1 being the most cold-responsive, as a likely consequence of the reduction of the ppGpp level that follows cold stress; (ii) a large increase in infB mRNA half-life and (iii) the cold-shock induced translational bias that ensures efficient translation of infB mRNA by the translational apparatus of cold shocked cells. A comparison of the mechanisms responsible for the cold shock induction of the three initiation factors is also presented. Oxford University Press 2019-05-21 2019-03-27 /pmc/articles/PMC6511841/ /pubmed/30916329 http://dx.doi.org/10.1093/nar/gkz187 Text en © The Author(s) 2019. Published by Oxford University Press on behalf of Nucleic Acids Research. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Molecular Biology
Brandi, Anna
Giangrossi, Mara
Paoloni, Silvia
Spurio, Roberto
Giuliodori, Anna M
Pon, Cynthia L
Gualerzi, Claudio O
Transcriptional and post-transcriptional events trigger de novo infB expression in cold stressed Escherichia coli
title Transcriptional and post-transcriptional events trigger de novo infB expression in cold stressed Escherichia coli
title_full Transcriptional and post-transcriptional events trigger de novo infB expression in cold stressed Escherichia coli
title_fullStr Transcriptional and post-transcriptional events trigger de novo infB expression in cold stressed Escherichia coli
title_full_unstemmed Transcriptional and post-transcriptional events trigger de novo infB expression in cold stressed Escherichia coli
title_short Transcriptional and post-transcriptional events trigger de novo infB expression in cold stressed Escherichia coli
title_sort transcriptional and post-transcriptional events trigger de novo infb expression in cold stressed escherichia coli
topic Molecular Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6511841/
https://www.ncbi.nlm.nih.gov/pubmed/30916329
http://dx.doi.org/10.1093/nar/gkz187
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