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Snapshot of iron response in Shewanella oneidensis by gene network reconstruction

BACKGROUND: Iron homeostasis of Shewanella oneidensis, a γ-proteobacterium possessing high iron content, is regulated by a global transcription factor Fur. However, knowledge is incomplete about other biological pathways that respond to changes in iron concentration, as well as details of the respon...

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Autores principales: Yang, Yunfeng, Harris, Daniel P, Luo, Feng, Xiong, Wenlu, Joachimiak, Marcin, Wu, Liyou, Dehal, Paramvir, Jacobsen, Janet, Yang, Zamin, Palumbo, Anthony V, Arkin, Adam P, Zhou, Jizhong
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2667191/
https://www.ncbi.nlm.nih.gov/pubmed/19321007
http://dx.doi.org/10.1186/1471-2164-10-131
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author Yang, Yunfeng
Harris, Daniel P
Luo, Feng
Xiong, Wenlu
Joachimiak, Marcin
Wu, Liyou
Dehal, Paramvir
Jacobsen, Janet
Yang, Zamin
Palumbo, Anthony V
Arkin, Adam P
Zhou, Jizhong
author_facet Yang, Yunfeng
Harris, Daniel P
Luo, Feng
Xiong, Wenlu
Joachimiak, Marcin
Wu, Liyou
Dehal, Paramvir
Jacobsen, Janet
Yang, Zamin
Palumbo, Anthony V
Arkin, Adam P
Zhou, Jizhong
author_sort Yang, Yunfeng
collection PubMed
description BACKGROUND: Iron homeostasis of Shewanella oneidensis, a γ-proteobacterium possessing high iron content, is regulated by a global transcription factor Fur. However, knowledge is incomplete about other biological pathways that respond to changes in iron concentration, as well as details of the responses. In this work, we integrate physiological, transcriptomics and genetic approaches to delineate the iron response of S. oneidensis. RESULTS: We show that the iron response in S. oneidensis is a rapid process. Temporal gene expression profiles were examined for iron depletion and repletion, and a gene co-expression network was reconstructed. Modules of iron acquisition systems, anaerobic energy metabolism and protein degradation were the most noteworthy in the gene network. Bioinformatics analyses suggested that genes in each of the modules might be regulated by DNA-binding proteins Fur, CRP and RpoH, respectively. Closer inspection of these modules revealed a transcriptional regulator (SO2426) involved in iron acquisition and ten transcriptional factors involved in anaerobic energy metabolism. Selected genes in the network were analyzed by genetic studies. Disruption of genes encoding a putative alcaligin biosynthesis protein (SO3032) and a gene previously implicated in protein degradation (SO2017) led to severe growth deficiency under iron depletion conditions. Disruption of a novel transcriptional factor (SO1415) caused deficiency in both anaerobic iron reduction and growth with thiosulfate or TMAO as an electronic acceptor, suggesting that SO1415 is required for specific branches of anaerobic energy metabolism pathways. CONCLUSION: Using a reconstructed gene network, we identified major biological pathways that were differentially expressed during iron depletion and repletion. Genetic studies not only demonstrated the importance of iron acquisition and protein degradation for iron depletion, but also characterized a novel transcriptional factor (SO1415) with a role in anaerobic energy metabolism.
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spelling pubmed-26671912009-04-09 Snapshot of iron response in Shewanella oneidensis by gene network reconstruction Yang, Yunfeng Harris, Daniel P Luo, Feng Xiong, Wenlu Joachimiak, Marcin Wu, Liyou Dehal, Paramvir Jacobsen, Janet Yang, Zamin Palumbo, Anthony V Arkin, Adam P Zhou, Jizhong BMC Genomics Research Article BACKGROUND: Iron homeostasis of Shewanella oneidensis, a γ-proteobacterium possessing high iron content, is regulated by a global transcription factor Fur. However, knowledge is incomplete about other biological pathways that respond to changes in iron concentration, as well as details of the responses. In this work, we integrate physiological, transcriptomics and genetic approaches to delineate the iron response of S. oneidensis. RESULTS: We show that the iron response in S. oneidensis is a rapid process. Temporal gene expression profiles were examined for iron depletion and repletion, and a gene co-expression network was reconstructed. Modules of iron acquisition systems, anaerobic energy metabolism and protein degradation were the most noteworthy in the gene network. Bioinformatics analyses suggested that genes in each of the modules might be regulated by DNA-binding proteins Fur, CRP and RpoH, respectively. Closer inspection of these modules revealed a transcriptional regulator (SO2426) involved in iron acquisition and ten transcriptional factors involved in anaerobic energy metabolism. Selected genes in the network were analyzed by genetic studies. Disruption of genes encoding a putative alcaligin biosynthesis protein (SO3032) and a gene previously implicated in protein degradation (SO2017) led to severe growth deficiency under iron depletion conditions. Disruption of a novel transcriptional factor (SO1415) caused deficiency in both anaerobic iron reduction and growth with thiosulfate or TMAO as an electronic acceptor, suggesting that SO1415 is required for specific branches of anaerobic energy metabolism pathways. CONCLUSION: Using a reconstructed gene network, we identified major biological pathways that were differentially expressed during iron depletion and repletion. Genetic studies not only demonstrated the importance of iron acquisition and protein degradation for iron depletion, but also characterized a novel transcriptional factor (SO1415) with a role in anaerobic energy metabolism. BioMed Central 2009-03-25 /pmc/articles/PMC2667191/ /pubmed/19321007 http://dx.doi.org/10.1186/1471-2164-10-131 Text en Copyright © 2009 Yang et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Yang, Yunfeng
Harris, Daniel P
Luo, Feng
Xiong, Wenlu
Joachimiak, Marcin
Wu, Liyou
Dehal, Paramvir
Jacobsen, Janet
Yang, Zamin
Palumbo, Anthony V
Arkin, Adam P
Zhou, Jizhong
Snapshot of iron response in Shewanella oneidensis by gene network reconstruction
title Snapshot of iron response in Shewanella oneidensis by gene network reconstruction
title_full Snapshot of iron response in Shewanella oneidensis by gene network reconstruction
title_fullStr Snapshot of iron response in Shewanella oneidensis by gene network reconstruction
title_full_unstemmed Snapshot of iron response in Shewanella oneidensis by gene network reconstruction
title_short Snapshot of iron response in Shewanella oneidensis by gene network reconstruction
title_sort snapshot of iron response in shewanella oneidensis by gene network reconstruction
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2667191/
https://www.ncbi.nlm.nih.gov/pubmed/19321007
http://dx.doi.org/10.1186/1471-2164-10-131
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