Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Rasmussen, Rebecca A, Wang, Suning, Camarillo, Jeannie M, Sosnowski, Victoria, Cho, Byoung-Kyu, Goo, Young Ah, Lucks, Julius B, O’Halloran, Thomas V
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
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
_version_ 1784866582383558656
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
work_keys_str_mv AT rasmussenrebeccaa zurandzincincreaseexpressionofecoliribosomalproteinl31throughrnamediatedrepressionoftherepressorl31p
AT wangsuning zurandzincincreaseexpressionofecoliribosomalproteinl31throughrnamediatedrepressionoftherepressorl31p
AT camarillojeanniem zurandzincincreaseexpressionofecoliribosomalproteinl31throughrnamediatedrepressionoftherepressorl31p
AT sosnowskivictoria zurandzincincreaseexpressionofecoliribosomalproteinl31throughrnamediatedrepressionoftherepressorl31p
AT chobyoungkyu zurandzincincreaseexpressionofecoliribosomalproteinl31throughrnamediatedrepressionoftherepressorl31p
AT gooyoungah zurandzincincreaseexpressionofecoliribosomalproteinl31throughrnamediatedrepressionoftherepressorl31p
AT lucksjuliusb zurandzincincreaseexpressionofecoliribosomalproteinl31throughrnamediatedrepressionoftherepressorl31p
AT ohalloranthomasv zurandzincincreaseexpressionofecoliribosomalproteinl31throughrnamediatedrepressionoftherepressorl31p