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Zur and zinc increase expression of E. coli ribosomal protein L31 through RNA-mediated repression of the repressor L31p
Bacteria can adapt in response to numerous stress conditions. One such stress condition is zinc depletion. The zinc-sensing transcription factor Zur regulates the way numerous bacterial species respond to severe changes in zinc availability. Under zinc sufficient conditions, Zn-loaded Zur (Zn(2)-Zur...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9825181/ https://www.ncbi.nlm.nih.gov/pubmed/36533433 http://dx.doi.org/10.1093/nar/gkac1086 |
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author | Rasmussen, Rebecca A Wang, Suning Camarillo, Jeannie M Sosnowski, Victoria Cho, Byoung-Kyu Goo, Young Ah Lucks, Julius B O’Halloran, Thomas V |
author_facet | Rasmussen, Rebecca A Wang, Suning Camarillo, Jeannie M Sosnowski, Victoria Cho, Byoung-Kyu Goo, Young Ah Lucks, Julius B O’Halloran, Thomas V |
author_sort | Rasmussen, Rebecca A |
collection | PubMed |
description | Bacteria can adapt in response to numerous stress conditions. One such stress condition is zinc depletion. The zinc-sensing transcription factor Zur regulates the way numerous bacterial species respond to severe changes in zinc availability. Under zinc sufficient conditions, Zn-loaded Zur (Zn(2)-Zur) is well-known to repress transcription of genes encoding zinc uptake transporters and paralogues of a few ribosomal proteins. Here, we report the discovery and mechanistic basis for the ability of Zur to up-regulate expression of the ribosomal protein L31 in response to zinc in E. coli. Through genetic mutations and reporter gene assays, we find that Zur achieves the up-regulation of L31 through a double repression cascade by which Zur first represses the transcription of L31p, a zinc-lacking paralogue of L31, which in turn represses the translation of L31. Mutational analyses show that translational repression by L31p requires an RNA hairpin structure within the l31 mRNA and involves the N-terminus of the L31p protein. This work uncovers a new genetic network that allows bacteria to respond to host-induced nutrient limiting conditions through a sophisticated ribosomal protein switching mechanism. |
format | Online Article Text |
id | pubmed-9825181 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-98251812023-01-09 Zur and zinc increase expression of E. coli ribosomal protein L31 through RNA-mediated repression of the repressor L31p Rasmussen, Rebecca A Wang, Suning Camarillo, Jeannie M Sosnowski, Victoria Cho, Byoung-Kyu Goo, Young Ah Lucks, Julius B O’Halloran, Thomas V Nucleic Acids Res Gene regulation, Chromatin and Epigenetics Bacteria can adapt in response to numerous stress conditions. One such stress condition is zinc depletion. The zinc-sensing transcription factor Zur regulates the way numerous bacterial species respond to severe changes in zinc availability. Under zinc sufficient conditions, Zn-loaded Zur (Zn(2)-Zur) is well-known to repress transcription of genes encoding zinc uptake transporters and paralogues of a few ribosomal proteins. Here, we report the discovery and mechanistic basis for the ability of Zur to up-regulate expression of the ribosomal protein L31 in response to zinc in E. coli. Through genetic mutations and reporter gene assays, we find that Zur achieves the up-regulation of L31 through a double repression cascade by which Zur first represses the transcription of L31p, a zinc-lacking paralogue of L31, which in turn represses the translation of L31. Mutational analyses show that translational repression by L31p requires an RNA hairpin structure within the l31 mRNA and involves the N-terminus of the L31p protein. This work uncovers a new genetic network that allows bacteria to respond to host-induced nutrient limiting conditions through a sophisticated ribosomal protein switching mechanism. Oxford University Press 2022-12-19 /pmc/articles/PMC9825181/ /pubmed/36533433 http://dx.doi.org/10.1093/nar/gkac1086 Text en © The Author(s) 2022. Published by Oxford University Press on behalf of Nucleic Acids Research. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Gene regulation, Chromatin and Epigenetics Rasmussen, Rebecca A Wang, Suning Camarillo, Jeannie M Sosnowski, Victoria Cho, Byoung-Kyu Goo, Young Ah Lucks, Julius B O’Halloran, Thomas V Zur and zinc increase expression of E. coli ribosomal protein L31 through RNA-mediated repression of the repressor L31p |
title | Zur and zinc increase expression of E. coli ribosomal protein L31 through RNA-mediated repression of the repressor L31p |
title_full | Zur and zinc increase expression of E. coli ribosomal protein L31 through RNA-mediated repression of the repressor L31p |
title_fullStr | Zur and zinc increase expression of E. coli ribosomal protein L31 through RNA-mediated repression of the repressor L31p |
title_full_unstemmed | Zur and zinc increase expression of E. coli ribosomal protein L31 through RNA-mediated repression of the repressor L31p |
title_short | Zur and zinc increase expression of E. coli ribosomal protein L31 through RNA-mediated repression of the repressor L31p |
title_sort | zur and zinc increase expression of e. coli ribosomal protein l31 through rna-mediated repression of the repressor l31p |
topic | Gene regulation, Chromatin and Epigenetics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9825181/ https://www.ncbi.nlm.nih.gov/pubmed/36533433 http://dx.doi.org/10.1093/nar/gkac1086 |
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