Phase Variation in Salmonella: Genetic Analysis of a Recombinational Switch
The alternative expression of Salmonella genes H1 and H2, which specify different flagellar antigens, results in the oscillation of phenotype known as phase variation. This alternation is controlled by the inversion of an 800-base-pair sequence of DNA adjacent to, or including part of, the H2 gene....
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Veröffentlicht in: | Proceedings of the National Academy of Sciences - PNAS 1979-01, Vol.76 (1), p.391-395 |
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creator | Silverman, Michael Zieg, Janine Hilmen, Marcia Simon, Melvin |
description | The alternative expression of Salmonella genes H1 and H2, which specify different flagellar antigens, results in the oscillation of phenotype known as phase variation. This alternation is controlled by the inversion of an 800-base-pair sequence of DNA adjacent to, or including part of, the H2 gene. The invertable region was presumed to regulate the function of a promoter and to include specific sites at which a recombinational event, resulting in the inversion, could occur. Here we report genetic manipulations of hybrid λ phage carrying the H2 gene that were used to define the H2 promoter region and the recombinational sites. The H2 gene fragment was inserted on a hybrid λ phage next to the cheW gene, which lacked a promoter element. In the resulting fusion, cheW gene activity was restored, the expression of the H2 and cheW genes was controlled coordinately by the inversion, and the polarity of transcription and location of the H2 gene could be determined. Evidence from this type of gene fusion suggested that the H2 gene promoter is included in the inversion region. Hybrid H2 phage were constructed that contained substitutions for regions of the H2 gene. In contrast to hybrid λ containing the H2 gene, which alternate between ``on'' and ``off'' states, several substituted λ H2 were fixed in the ``on'' state. A site necessary for the recombinational event must have been removed in these fixed λ H2. |
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This alternation is controlled by the inversion of an 800-base-pair sequence of DNA adjacent to, or including part of, the H2 gene. The invertable region was presumed to regulate the function of a promoter and to include specific sites at which a recombinational event, resulting in the inversion, could occur. Here we report genetic manipulations of hybrid λ phage carrying the H2 gene that were used to define the H2 promoter region and the recombinational sites. The H2 gene fragment was inserted on a hybrid λ phage next to the cheW gene, which lacked a promoter element. In the resulting fusion, cheW gene activity was restored, the expression of the H2 and cheW genes was controlled coordinately by the inversion, and the polarity of transcription and location of the H2 gene could be determined. Evidence from this type of gene fusion suggested that the H2 gene promoter is included in the inversion region. Hybrid H2 phage were constructed that contained substitutions for regions of the H2 gene. In contrast to hybrid λ containing the H2 gene, which alternate between ``on'' and ``off'' states, several substituted λ H2 were fixed in the ``on'' state. A site necessary for the recombinational event must have been removed in these fixed λ H2.</description><identifier>ISSN: 0027-8424</identifier><identifier>EISSN: 1091-6490</identifier><identifier>DOI: 10.1073/pnas.76.1.391</identifier><identifier>PMID: 370828</identifier><language>eng</language><publisher>United States: National Academy of Sciences of the United States of America</publisher><subject>Bacterial Proteins - genetics ; Bacteriophages ; Chromosome Inversion ; DNA ; DNA, Recombinant ; Escherichia coli - genetics ; Flagellin - genetics ; Gene expression regulation ; Genes ; Genes, Regulator ; Genetic variation ; Hybridity ; Operator regions ; Operon ; Plasmids ; Promoter regions ; Recombination, Genetic ; Salmonella ; Salmonella - genetics</subject><ispartof>Proceedings of the National Academy of Sciences - PNAS, 1979-01, Vol.76 (1), p.391-395</ispartof><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c516t-9deb8d77365315a3a57ec468e5a13f83eda98a7a456139f5be85f61411f78e133</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Uhttp://www.pnas.org/content/76/1.cover.gif</thumbnail><linktopdf>$$Uhttps://www.jstor.org/stable/pdf/69501$$EPDF$$P50$$Gjstor$$H</linktopdf><linktohtml>$$Uhttps://www.jstor.org/stable/69501$$EHTML$$P50$$Gjstor$$H</linktohtml><link.rule.ids>230,314,727,780,784,803,885,27924,27925,53791,53793,58017,58250</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/370828$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Silverman, Michael</creatorcontrib><creatorcontrib>Zieg, Janine</creatorcontrib><creatorcontrib>Hilmen, Marcia</creatorcontrib><creatorcontrib>Simon, Melvin</creatorcontrib><title>Phase Variation in Salmonella: Genetic Analysis of a Recombinational Switch</title><title>Proceedings of the National Academy of Sciences - PNAS</title><addtitle>Proc Natl Acad Sci U S A</addtitle><description>The alternative expression of Salmonella genes H1 and H2, which specify different flagellar antigens, results in the oscillation of phenotype known as phase variation. This alternation is controlled by the inversion of an 800-base-pair sequence of DNA adjacent to, or including part of, the H2 gene. The invertable region was presumed to regulate the function of a promoter and to include specific sites at which a recombinational event, resulting in the inversion, could occur. Here we report genetic manipulations of hybrid λ phage carrying the H2 gene that were used to define the H2 promoter region and the recombinational sites. The H2 gene fragment was inserted on a hybrid λ phage next to the cheW gene, which lacked a promoter element. In the resulting fusion, cheW gene activity was restored, the expression of the H2 and cheW genes was controlled coordinately by the inversion, and the polarity of transcription and location of the H2 gene could be determined. Evidence from this type of gene fusion suggested that the H2 gene promoter is included in the inversion region. Hybrid H2 phage were constructed that contained substitutions for regions of the H2 gene. In contrast to hybrid λ containing the H2 gene, which alternate between ``on'' and ``off'' states, several substituted λ H2 were fixed in the ``on'' state. A site necessary for the recombinational event must have been removed in these fixed λ H2.</description><subject>Bacterial Proteins - genetics</subject><subject>Bacteriophages</subject><subject>Chromosome Inversion</subject><subject>DNA</subject><subject>DNA, Recombinant</subject><subject>Escherichia coli - genetics</subject><subject>Flagellin - genetics</subject><subject>Gene expression regulation</subject><subject>Genes</subject><subject>Genes, Regulator</subject><subject>Genetic variation</subject><subject>Hybridity</subject><subject>Operator regions</subject><subject>Operon</subject><subject>Plasmids</subject><subject>Promoter regions</subject><subject>Recombination, Genetic</subject><subject>Salmonella</subject><subject>Salmonella - genetics</subject><issn>0027-8424</issn><issn>1091-6490</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1979</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kD2PEzEQhi3EVzgoaRDFNtBt8MTfSBSnExyIk0Ac0FqTzSzxyWuHtQPcv2dDjig0VC7e55nxvIw9Bj4HbsSLTcIyN3oOc-HgFpsBd9Bq6fhtNuN8YVorF_I-e1DKFefcKcvvsbvCcLuwM_b-4xoLNV9xDFhDTk1IzSXGISeKEV8255Sohq45TRivSyhN7htsPlGXh2VIfxSMzeXPULv1Q3anx1jo0c17wr68ef357G178eH83dnpRdsp0LV1K1ralTFCKwEKBSpDndSWFILoraAVOosGpdIgXK-WZFWvQQL0xhIIccJe7edutsuBVh2lOmL0mzEMOF77jMH_m6Sw9t_yDy_swkk1-c9v_DF_31Kpfgil292bKG-LN1IakNpMYLsHuzGXMlJ_2AHc77r3u-690R781P3EPz3-2IHel30U76y_4ZH97D-x77cxVvpVJ-7JnrsqNY8HUDvFQfwGUs6gsA</recordid><startdate>19790101</startdate><enddate>19790101</enddate><creator>Silverman, Michael</creator><creator>Zieg, Janine</creator><creator>Hilmen, Marcia</creator><creator>Simon, Melvin</creator><general>National Academy of Sciences of the United States of America</general><general>National Acad Sciences</general><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>7X8</scope><scope>5PM</scope></search><sort><creationdate>19790101</creationdate><title>Phase Variation in Salmonella: Genetic Analysis of a Recombinational Switch</title><author>Silverman, Michael ; Zieg, Janine ; Hilmen, Marcia ; Simon, Melvin</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c516t-9deb8d77365315a3a57ec468e5a13f83eda98a7a456139f5be85f61411f78e133</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1979</creationdate><topic>Bacterial Proteins - genetics</topic><topic>Bacteriophages</topic><topic>Chromosome Inversion</topic><topic>DNA</topic><topic>DNA, Recombinant</topic><topic>Escherichia coli - genetics</topic><topic>Flagellin - genetics</topic><topic>Gene expression regulation</topic><topic>Genes</topic><topic>Genes, Regulator</topic><topic>Genetic variation</topic><topic>Hybridity</topic><topic>Operator regions</topic><topic>Operon</topic><topic>Plasmids</topic><topic>Promoter regions</topic><topic>Recombination, Genetic</topic><topic>Salmonella</topic><topic>Salmonella - genetics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Silverman, Michael</creatorcontrib><creatorcontrib>Zieg, Janine</creatorcontrib><creatorcontrib>Hilmen, Marcia</creatorcontrib><creatorcontrib>Simon, Melvin</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</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>Silverman, Michael</au><au>Zieg, Janine</au><au>Hilmen, Marcia</au><au>Simon, Melvin</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Phase Variation in Salmonella: Genetic Analysis of a Recombinational Switch</atitle><jtitle>Proceedings of the National Academy of Sciences - PNAS</jtitle><addtitle>Proc Natl Acad Sci U S A</addtitle><date>1979-01-01</date><risdate>1979</risdate><volume>76</volume><issue>1</issue><spage>391</spage><epage>395</epage><pages>391-395</pages><issn>0027-8424</issn><eissn>1091-6490</eissn><abstract>The alternative expression of Salmonella genes H1 and H2, which specify different flagellar antigens, results in the oscillation of phenotype known as phase variation. This alternation is controlled by the inversion of an 800-base-pair sequence of DNA adjacent to, or including part of, the H2 gene. The invertable region was presumed to regulate the function of a promoter and to include specific sites at which a recombinational event, resulting in the inversion, could occur. Here we report genetic manipulations of hybrid λ phage carrying the H2 gene that were used to define the H2 promoter region and the recombinational sites. The H2 gene fragment was inserted on a hybrid λ phage next to the cheW gene, which lacked a promoter element. In the resulting fusion, cheW gene activity was restored, the expression of the H2 and cheW genes was controlled coordinately by the inversion, and the polarity of transcription and location of the H2 gene could be determined. Evidence from this type of gene fusion suggested that the H2 gene promoter is included in the inversion region. Hybrid H2 phage were constructed that contained substitutions for regions of the H2 gene. In contrast to hybrid λ containing the H2 gene, which alternate between ``on'' and ``off'' states, several substituted λ H2 were fixed in the ``on'' state. A site necessary for the recombinational event must have been removed in these fixed λ H2.</abstract><cop>United States</cop><pub>National Academy of Sciences of the United States of America</pub><pmid>370828</pmid><doi>10.1073/pnas.76.1.391</doi><tpages>5</tpages><oa>free_for_read</oa></addata></record> |
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source | MEDLINE; JSTOR Archive Collection A-Z Listing; PubMed Central; Alma/SFX Local Collection; Free Full-Text Journals in Chemistry |
subjects | Bacterial Proteins - genetics Bacteriophages Chromosome Inversion DNA DNA, Recombinant Escherichia coli - genetics Flagellin - genetics Gene expression regulation Genes Genes, Regulator Genetic variation Hybridity Operator regions Operon Plasmids Promoter regions Recombination, Genetic Salmonella Salmonella - genetics |
title | Phase Variation in Salmonella: Genetic Analysis of a Recombinational Switch |
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