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Regulation of the Expression of the Vibrio parahaemolyticus peuA Gene Encoding an Alternative Ferric Enterobactin Receptor

A pvsB-vctA-irgA triple deletion mutant of Vibrio parahaemolyticus can utilize enterobactin under iron-limiting conditions by inducing a previously undescribed receptor, PeuA (VPA0150), in response to extracellular alkaline pH and enterobactin. In silico analyses revealed the existence of a two-comp...

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Autores principales: Tanabe, Tomotaka, Kato, Ayaka, Shiuchi, Keiichi, Miyamoto, Katsushiro, Tsujibo, Hiroshi, Maki, Jun, Yamamoto, Shigeo, Funahashi, Tatsuya
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4141801/
https://www.ncbi.nlm.nih.gov/pubmed/25148374
http://dx.doi.org/10.1371/journal.pone.0105749
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author Tanabe, Tomotaka
Kato, Ayaka
Shiuchi, Keiichi
Miyamoto, Katsushiro
Tsujibo, Hiroshi
Maki, Jun
Yamamoto, Shigeo
Funahashi, Tatsuya
author_facet Tanabe, Tomotaka
Kato, Ayaka
Shiuchi, Keiichi
Miyamoto, Katsushiro
Tsujibo, Hiroshi
Maki, Jun
Yamamoto, Shigeo
Funahashi, Tatsuya
author_sort Tanabe, Tomotaka
collection PubMed
description A pvsB-vctA-irgA triple deletion mutant of Vibrio parahaemolyticus can utilize enterobactin under iron-limiting conditions by inducing a previously undescribed receptor, PeuA (VPA0150), in response to extracellular alkaline pH and enterobactin. In silico analyses revealed the existence of a two-component regulatory system operon, peuRS, immediately upstream of peuA, which constitutes an operon with the TonB2 system genes. Both the peuRS and peuA-tonB2 operons were found to be upregulated under iron-limiting conditions in a ferric uptake regulator (Fur)-dependent manner. The involvement of peuA and peuRS in enterobactin utilization was analyzed by complementation experiments using deletion mutants. Primer extension analysis indicated that, under iron-limiting conditions, the transcription of peuA was initiated from the +1 site at pH 7.0 and from both the +1 and +39 sites at pH 8.0 in the presence of enterobactin. The +39 transcript was absent from the peuRS deletion mutant. Secondary structure prediction of their 5′-untranslated regions suggested that translation initiation is blocked in the +1 transcript, but not in the +39 transcript. Consistent with this, in vitro translation analysis demonstrated that production of PeuA was determined only by the +39 transcript. These studies establish a novel gene regulation mechanism in which the two-component regulatory system PeuRS enhances expression of the alternative +39 transcript that possesses non-inhibitory structure, allowing the peuA expression to be regulated at the translation stage.
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spelling pubmed-41418012014-08-25 Regulation of the Expression of the Vibrio parahaemolyticus peuA Gene Encoding an Alternative Ferric Enterobactin Receptor Tanabe, Tomotaka Kato, Ayaka Shiuchi, Keiichi Miyamoto, Katsushiro Tsujibo, Hiroshi Maki, Jun Yamamoto, Shigeo Funahashi, Tatsuya PLoS One Research Article A pvsB-vctA-irgA triple deletion mutant of Vibrio parahaemolyticus can utilize enterobactin under iron-limiting conditions by inducing a previously undescribed receptor, PeuA (VPA0150), in response to extracellular alkaline pH and enterobactin. In silico analyses revealed the existence of a two-component regulatory system operon, peuRS, immediately upstream of peuA, which constitutes an operon with the TonB2 system genes. Both the peuRS and peuA-tonB2 operons were found to be upregulated under iron-limiting conditions in a ferric uptake regulator (Fur)-dependent manner. The involvement of peuA and peuRS in enterobactin utilization was analyzed by complementation experiments using deletion mutants. Primer extension analysis indicated that, under iron-limiting conditions, the transcription of peuA was initiated from the +1 site at pH 7.0 and from both the +1 and +39 sites at pH 8.0 in the presence of enterobactin. The +39 transcript was absent from the peuRS deletion mutant. Secondary structure prediction of their 5′-untranslated regions suggested that translation initiation is blocked in the +1 transcript, but not in the +39 transcript. Consistent with this, in vitro translation analysis demonstrated that production of PeuA was determined only by the +39 transcript. These studies establish a novel gene regulation mechanism in which the two-component regulatory system PeuRS enhances expression of the alternative +39 transcript that possesses non-inhibitory structure, allowing the peuA expression to be regulated at the translation stage. Public Library of Science 2014-08-22 /pmc/articles/PMC4141801/ /pubmed/25148374 http://dx.doi.org/10.1371/journal.pone.0105749 Text en © 2014 Tanabe 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
Tanabe, Tomotaka
Kato, Ayaka
Shiuchi, Keiichi
Miyamoto, Katsushiro
Tsujibo, Hiroshi
Maki, Jun
Yamamoto, Shigeo
Funahashi, Tatsuya
Regulation of the Expression of the Vibrio parahaemolyticus peuA Gene Encoding an Alternative Ferric Enterobactin Receptor
title Regulation of the Expression of the Vibrio parahaemolyticus peuA Gene Encoding an Alternative Ferric Enterobactin Receptor
title_full Regulation of the Expression of the Vibrio parahaemolyticus peuA Gene Encoding an Alternative Ferric Enterobactin Receptor
title_fullStr Regulation of the Expression of the Vibrio parahaemolyticus peuA Gene Encoding an Alternative Ferric Enterobactin Receptor
title_full_unstemmed Regulation of the Expression of the Vibrio parahaemolyticus peuA Gene Encoding an Alternative Ferric Enterobactin Receptor
title_short Regulation of the Expression of the Vibrio parahaemolyticus peuA Gene Encoding an Alternative Ferric Enterobactin Receptor
title_sort regulation of the expression of the vibrio parahaemolyticus peua gene encoding an alternative ferric enterobactin receptor
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4141801/
https://www.ncbi.nlm.nih.gov/pubmed/25148374
http://dx.doi.org/10.1371/journal.pone.0105749
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