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Mapping the Regulatory Network for Salmonella enterica Serovar Typhimurium Invasion
Salmonella enterica pathogenicity island 1 (SPI-1) encodes proteins required for invasion of gut epithelial cells. The timing of invasion is tightly controlled by a complex regulatory network. The transcription factor (TF) HilD is the master regulator of this process and senses environmental signals...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society for Microbiology
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5013294/ https://www.ncbi.nlm.nih.gov/pubmed/27601571 http://dx.doi.org/10.1128/mBio.01024-16 |
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author | Smith, Carol Stringer, Anne M. Mao, Chunhong Palumbo, Michael J. Wade, Joseph T. |
author_facet | Smith, Carol Stringer, Anne M. Mao, Chunhong Palumbo, Michael J. Wade, Joseph T. |
author_sort | Smith, Carol |
collection | PubMed |
description | Salmonella enterica pathogenicity island 1 (SPI-1) encodes proteins required for invasion of gut epithelial cells. The timing of invasion is tightly controlled by a complex regulatory network. The transcription factor (TF) HilD is the master regulator of this process and senses environmental signals associated with invasion. HilD activates transcription of genes within and outside SPI-1, including six other TFs. Thus, the transcriptional program associated with host cell invasion is controlled by at least 7 TFs. However, very few of the regulatory targets are known for these TFs, and the extent of the regulatory network is unclear. In this study, we used complementary genomic approaches to map the direct regulatory targets of all 7 TFs. Our data reveal a highly complex and interconnected network that includes many previously undescribed regulatory targets. Moreover, the network extends well beyond the 7 TFs, due to the inclusion of many additional TFs and noncoding RNAs. By comparing gene expression profiles of regulatory targets for the 7 TFs, we identified many uncharacterized genes that are likely to play direct roles in invasion. We also uncovered cross talk between SPI-1 regulation and other regulatory pathways, which, in turn, identified gene clusters that likely share related functions. Our data are freely available through an intuitive online browser and represent a valuable resource for the bacterial research community. |
format | Online Article Text |
id | pubmed-5013294 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | American Society for Microbiology |
record_format | MEDLINE/PubMed |
spelling | pubmed-50132942016-09-16 Mapping the Regulatory Network for Salmonella enterica Serovar Typhimurium Invasion Smith, Carol Stringer, Anne M. Mao, Chunhong Palumbo, Michael J. Wade, Joseph T. mBio Research Article Salmonella enterica pathogenicity island 1 (SPI-1) encodes proteins required for invasion of gut epithelial cells. The timing of invasion is tightly controlled by a complex regulatory network. The transcription factor (TF) HilD is the master regulator of this process and senses environmental signals associated with invasion. HilD activates transcription of genes within and outside SPI-1, including six other TFs. Thus, the transcriptional program associated with host cell invasion is controlled by at least 7 TFs. However, very few of the regulatory targets are known for these TFs, and the extent of the regulatory network is unclear. In this study, we used complementary genomic approaches to map the direct regulatory targets of all 7 TFs. Our data reveal a highly complex and interconnected network that includes many previously undescribed regulatory targets. Moreover, the network extends well beyond the 7 TFs, due to the inclusion of many additional TFs and noncoding RNAs. By comparing gene expression profiles of regulatory targets for the 7 TFs, we identified many uncharacterized genes that are likely to play direct roles in invasion. We also uncovered cross talk between SPI-1 regulation and other regulatory pathways, which, in turn, identified gene clusters that likely share related functions. Our data are freely available through an intuitive online browser and represent a valuable resource for the bacterial research community. American Society for Microbiology 2016-09-06 /pmc/articles/PMC5013294/ /pubmed/27601571 http://dx.doi.org/10.1128/mBio.01024-16 Text en Copyright © 2016 Smith et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (http://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Research Article Smith, Carol Stringer, Anne M. Mao, Chunhong Palumbo, Michael J. Wade, Joseph T. Mapping the Regulatory Network for Salmonella enterica Serovar Typhimurium Invasion |
title | Mapping the Regulatory Network for Salmonella enterica Serovar Typhimurium Invasion |
title_full | Mapping the Regulatory Network for Salmonella enterica Serovar Typhimurium Invasion |
title_fullStr | Mapping the Regulatory Network for Salmonella enterica Serovar Typhimurium Invasion |
title_full_unstemmed | Mapping the Regulatory Network for Salmonella enterica Serovar Typhimurium Invasion |
title_short | Mapping the Regulatory Network for Salmonella enterica Serovar Typhimurium Invasion |
title_sort | mapping the regulatory network for salmonella enterica serovar typhimurium invasion |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5013294/ https://www.ncbi.nlm.nih.gov/pubmed/27601571 http://dx.doi.org/10.1128/mBio.01024-16 |
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