H-NS family members function coordinately in an opportunistic pathogen
The histone-like nucleoid structuring protein, H-NS, is a prominent global regulator of gene expression. Many Gram-negative bacteria contain multiple members of the H-NS family of proteins. Thus, a key question is whether H-NS family members have overlapping or distinct functions. To address this qu...
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Veröffentlicht in: | Proceedings of the National Academy of Sciences - PNAS 2008-12, Vol.105 (48), p.18947-18952 |
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container_title | Proceedings of the National Academy of Sciences - PNAS |
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creator | Castang, Sandra McManus, Heather R Turner, Keith H Dove, Simon L |
description | The histone-like nucleoid structuring protein, H-NS, is a prominent global regulator of gene expression. Many Gram-negative bacteria contain multiple members of the H-NS family of proteins. Thus, a key question is whether H-NS family members have overlapping or distinct functions. To address this question we performed genome-wide location analyses with MvaT and MvaU, the two H-NS family members present in Pseudomonas aeruginosa. We show that MvaT and MvaU bind the same chromosomal regions, coregulating the expression of [almost equal to]350 target genes. We show further that like H-NS in enteric bacteria, which functions as a transcriptional silencer of foreign DNA by binding to AT-rich elements, MvaT and MvaU bind preferentially to AT-rich regions of the chromosome. Our findings establish that H-NS paralogs can function coordinately to regulate expression of the same set of target genes, and suggest that MvaT and MvaU are involved in silencing foreign DNA elements in P. aeruginosa. |
doi_str_mv | 10.1073/pnas.0808215105 |
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Many Gram-negative bacteria contain multiple members of the H-NS family of proteins. Thus, a key question is whether H-NS family members have overlapping or distinct functions. To address this question we performed genome-wide location analyses with MvaT and MvaU, the two H-NS family members present in Pseudomonas aeruginosa. We show that MvaT and MvaU bind the same chromosomal regions, coregulating the expression of [almost equal to]350 target genes. We show further that like H-NS in enteric bacteria, which functions as a transcriptional silencer of foreign DNA by binding to AT-rich elements, MvaT and MvaU bind preferentially to AT-rich regions of the chromosome. Our findings establish that H-NS paralogs can function coordinately to regulate expression of the same set of target genes, and suggest that MvaT and MvaU are involved in silencing foreign DNA elements in P. aeruginosa.</description><identifier>ISSN: 0027-8424</identifier><identifier>EISSN: 1091-6490</identifier><identifier>DOI: 10.1073/pnas.0808215105</identifier><identifier>PMID: 19028873</identifier><language>eng</language><publisher>United States: National Academy of Sciences</publisher><subject>Bacteria ; Bacterial Proteins - genetics ; Bacterial Proteins - metabolism ; Biological Sciences ; Chromosomes ; Chromosomes, Bacterial ; Deoxyribonucleic acid ; DNA ; DNA-Binding Proteins - genetics ; DNA-Binding Proteins - metabolism ; Family members ; Gene expression ; Gene expression regulation ; Gene Expression Regulation, Bacterial ; Gene Silencing ; Genes ; Genomes ; Genomics ; Humans ; Proteins ; Pseudomonas aeruginosa ; Pseudomonas aeruginosa - genetics ; Pseudomonas aeruginosa - metabolism ; Pseudomonas aeruginosa - pathogenicity ; Regulator genes ; Regulon ; Trans-Activators - genetics ; Trans-Activators - metabolism ; Transcription, Genetic</subject><ispartof>Proceedings of the National Academy of Sciences - PNAS, 2008-12, Vol.105 (48), p.18947-18952</ispartof><rights>Copyright 2008 The National Academy of Sciences of the United States of America</rights><rights>Copyright National Academy of Sciences Dec 2, 2008</rights><rights>2008 by The National Academy of Sciences of the USA</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c620t-5b2b87a9f590b3a43fe625c236dfcaae8a7046e0442abe034c4f941dffd1dd993</citedby><cites>FETCH-LOGICAL-c620t-5b2b87a9f590b3a43fe625c236dfcaae8a7046e0442abe034c4f941dffd1dd993</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Uhttp://www.pnas.org/content/105/48.cover.gif</thumbnail><linktopdf>$$Uhttps://www.jstor.org/stable/pdf/25465572$$EPDF$$P50$$Gjstor$$H</linktopdf><linktohtml>$$Uhttps://www.jstor.org/stable/25465572$$EHTML$$P50$$Gjstor$$H</linktohtml><link.rule.ids>230,314,723,776,780,799,881,27903,27904,53769,53771,57995,58228</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19028873$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Castang, Sandra</creatorcontrib><creatorcontrib>McManus, Heather R</creatorcontrib><creatorcontrib>Turner, Keith H</creatorcontrib><creatorcontrib>Dove, Simon L</creatorcontrib><title>H-NS family members function coordinately in an opportunistic pathogen</title><title>Proceedings of the National Academy of Sciences - PNAS</title><addtitle>Proc Natl Acad Sci U S A</addtitle><description>The histone-like nucleoid structuring protein, H-NS, is a prominent global regulator of gene expression. Many Gram-negative bacteria contain multiple members of the H-NS family of proteins. Thus, a key question is whether H-NS family members have overlapping or distinct functions. To address this question we performed genome-wide location analyses with MvaT and MvaU, the two H-NS family members present in Pseudomonas aeruginosa. We show that MvaT and MvaU bind the same chromosomal regions, coregulating the expression of [almost equal to]350 target genes. We show further that like H-NS in enteric bacteria, which functions as a transcriptional silencer of foreign DNA by binding to AT-rich elements, MvaT and MvaU bind preferentially to AT-rich regions of the chromosome. Our findings establish that H-NS paralogs can function coordinately to regulate expression of the same set of target genes, and suggest that MvaT and MvaU are involved in silencing foreign DNA elements in P. aeruginosa.</description><subject>Bacteria</subject><subject>Bacterial Proteins - genetics</subject><subject>Bacterial Proteins - metabolism</subject><subject>Biological Sciences</subject><subject>Chromosomes</subject><subject>Chromosomes, Bacterial</subject><subject>Deoxyribonucleic acid</subject><subject>DNA</subject><subject>DNA-Binding Proteins - genetics</subject><subject>DNA-Binding Proteins - metabolism</subject><subject>Family members</subject><subject>Gene expression</subject><subject>Gene expression regulation</subject><subject>Gene Expression Regulation, Bacterial</subject><subject>Gene Silencing</subject><subject>Genes</subject><subject>Genomes</subject><subject>Genomics</subject><subject>Humans</subject><subject>Proteins</subject><subject>Pseudomonas aeruginosa</subject><subject>Pseudomonas aeruginosa - genetics</subject><subject>Pseudomonas aeruginosa - metabolism</subject><subject>Pseudomonas aeruginosa - pathogenicity</subject><subject>Regulator genes</subject><subject>Regulon</subject><subject>Trans-Activators - genetics</subject><subject>Trans-Activators - metabolism</subject><subject>Transcription, Genetic</subject><issn>0027-8424</issn><issn>1091-6490</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkUFv1DAQhS0EokvhzAmIOCBxSDt27MS-VEIVbZEqOJSeLcext14ldrAdRP89Xu2qW7j0NIf3zdPMewi9xXCCoWtOZ6_SCXDgBDMM7BlaYRC4bqmA52gFQLqaU0KP0KuUNgAgGIeX6AgLIJx3zQpdXNXfbyqrJjfeV5OZehNTZRevswu-0iHEwXmVTVGdr5SvwjyHmBfvUna6mlW-C2vjX6MXVo3JvNnPY3R78fXn-VV9_ePy2_mX61q3BHLNetLzTgnLBPSNoo01LWGaNO1gtVKGqw5oa4BSonoDDdXUCooHawc8DEI0x-hs5zsv_WQGbXyOapRzdJOK9zIoJ_9VvLuT6_BbEiZaQppi8GlvEMOvxaQsJ5e0GUflTViSbAUvJHsaJBhK1AQX8ON_4CYs0ZcUJAHcCEZhe_fpDtIxpBSNfTgZg9w2KbdNykOTZeP9408P_L66AlR7YLt5sGOScom5oF1BPj-BSLuMYzZ_cmHf7dhNyiE-wITRlrGOFP3DTrcqSLWOLsnbm-2DgFnbYU6bv_Iixjs</recordid><startdate>20081202</startdate><enddate>20081202</enddate><creator>Castang, Sandra</creator><creator>McManus, Heather R</creator><creator>Turner, Keith H</creator><creator>Dove, Simon L</creator><general>National Academy of Sciences</general><general>National Acad Sciences</general><scope>FBQ</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QG</scope><scope>7QL</scope><scope>7QP</scope><scope>7QR</scope><scope>7SN</scope><scope>7SS</scope><scope>7T5</scope><scope>7TK</scope><scope>7TM</scope><scope>7TO</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>M7N</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20081202</creationdate><title>H-NS family members function coordinately in an opportunistic pathogen</title><author>Castang, Sandra ; McManus, Heather R ; Turner, Keith H ; Dove, Simon L</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c620t-5b2b87a9f590b3a43fe625c236dfcaae8a7046e0442abe034c4f941dffd1dd993</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>Bacteria</topic><topic>Bacterial Proteins - genetics</topic><topic>Bacterial Proteins - metabolism</topic><topic>Biological Sciences</topic><topic>Chromosomes</topic><topic>Chromosomes, Bacterial</topic><topic>Deoxyribonucleic acid</topic><topic>DNA</topic><topic>DNA-Binding Proteins - genetics</topic><topic>DNA-Binding Proteins - metabolism</topic><topic>Family members</topic><topic>Gene expression</topic><topic>Gene expression regulation</topic><topic>Gene Expression Regulation, Bacterial</topic><topic>Gene Silencing</topic><topic>Genes</topic><topic>Genomes</topic><topic>Genomics</topic><topic>Humans</topic><topic>Proteins</topic><topic>Pseudomonas aeruginosa</topic><topic>Pseudomonas aeruginosa - genetics</topic><topic>Pseudomonas aeruginosa - metabolism</topic><topic>Pseudomonas aeruginosa - pathogenicity</topic><topic>Regulator genes</topic><topic>Regulon</topic><topic>Trans-Activators - genetics</topic><topic>Trans-Activators - metabolism</topic><topic>Transcription, Genetic</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Castang, Sandra</creatorcontrib><creatorcontrib>McManus, Heather R</creatorcontrib><creatorcontrib>Turner, Keith H</creatorcontrib><creatorcontrib>Dove, Simon L</creatorcontrib><collection>AGRIS</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Animal Behavior Abstracts</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Ecology Abstracts</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Immunology Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Proceedings of the National Academy of Sciences - PNAS</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Castang, Sandra</au><au>McManus, Heather R</au><au>Turner, Keith H</au><au>Dove, Simon L</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>H-NS family members function coordinately in an opportunistic pathogen</atitle><jtitle>Proceedings of the National Academy of Sciences - PNAS</jtitle><addtitle>Proc Natl Acad Sci U S A</addtitle><date>2008-12-02</date><risdate>2008</risdate><volume>105</volume><issue>48</issue><spage>18947</spage><epage>18952</epage><pages>18947-18952</pages><issn>0027-8424</issn><eissn>1091-6490</eissn><abstract>The histone-like nucleoid structuring protein, H-NS, is a prominent global regulator of gene expression. Many Gram-negative bacteria contain multiple members of the H-NS family of proteins. Thus, a key question is whether H-NS family members have overlapping or distinct functions. To address this question we performed genome-wide location analyses with MvaT and MvaU, the two H-NS family members present in Pseudomonas aeruginosa. We show that MvaT and MvaU bind the same chromosomal regions, coregulating the expression of [almost equal to]350 target genes. We show further that like H-NS in enteric bacteria, which functions as a transcriptional silencer of foreign DNA by binding to AT-rich elements, MvaT and MvaU bind preferentially to AT-rich regions of the chromosome. 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subjects | Bacteria Bacterial Proteins - genetics Bacterial Proteins - metabolism Biological Sciences Chromosomes Chromosomes, Bacterial Deoxyribonucleic acid DNA DNA-Binding Proteins - genetics DNA-Binding Proteins - metabolism Family members Gene expression Gene expression regulation Gene Expression Regulation, Bacterial Gene Silencing Genes Genomes Genomics Humans Proteins Pseudomonas aeruginosa Pseudomonas aeruginosa - genetics Pseudomonas aeruginosa - metabolism Pseudomonas aeruginosa - pathogenicity Regulator genes Regulon Trans-Activators - genetics Trans-Activators - metabolism Transcription, Genetic |
title | H-NS family members function coordinately in an opportunistic pathogen |
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