Transcriptional regulation of type 4 pilin genes and the site-specific recombinase gene, piv, in Moraxella lacunata and Moraxella bovis

Moraxella lacunata and Moraxella bovis use type 4 pili to adhere to epithelial tissues of the cornea and conjunctiva. Primer extension analyses were used to map the transcriptional start sites for the genes encoding the major pilin subunits (tfpQ/I) and the DNA invertase (piv), which determines pili...

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Veröffentlicht in:Journal of Bacteriology 1997-12, Vol.179 (23), p.7298-7305
Hauptverfasser: Heinrich, D.W, Glasgow, A.C
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description Moraxella lacunata and Moraxella bovis use type 4 pili to adhere to epithelial tissues of the cornea and conjunctiva. Primer extension analyses were used to map the transcriptional start sites for the genes encoding the major pilin subunits (tfpQ/I) and the DNA invertase (piv), which determines pilin type expression. tfpQ/I transcription starts at a sigma 54-dependent promoter (tfpQ/Ip2) and, under certain growth conditions, this transcription is accompanied by weaker upstream transcription that starts at a potential sigma 70-dependent promoter (tfpQ/Ip1). piv is expressed in both M. lacunata and M. bovis from a putative sigma 70-dependent promoter (pivp) under all conditions assayed. sigma 54-dependent promoters require activators in order to initiate transcription; therefore, it is likely that tfpQ/Ip2 is also regulated by an activator in Moraxella. Primer extension assays with RNA isolated from Escherichia coli containing the subcloned pilin inversion region from M. lacunata showed that pivp is used for the expression of piv; however, tfpQ/Ip2 is not used for the transcription of tfpQ/I. Transcription from tfpQ/Ip2 was activated in E. coli when the sensor (PilS) and response regulator (PilR) proteins of type 4 pilin transcription in Pseudomonas aeruginosa were expressed from a plasmid. These results suggest that the expression of the type 4 pilin in M. lacunata and M. bovis is regulated not only by a site-specific DNA inversion system but also by a regulatory system which is functionally analogous to the PilS-PilR two-component system of P. aeruginosa
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Primer extension analyses were used to map the transcriptional start sites for the genes encoding the major pilin subunits (tfpQ/I) and the DNA invertase (piv), which determines pilin type expression. tfpQ/I transcription starts at a sigma 54-dependent promoter (tfpQ/Ip2) and, under certain growth conditions, this transcription is accompanied by weaker upstream transcription that starts at a potential sigma 70-dependent promoter (tfpQ/Ip1). piv is expressed in both M. lacunata and M. bovis from a putative sigma 70-dependent promoter (pivp) under all conditions assayed. sigma 54-dependent promoters require activators in order to initiate transcription; therefore, it is likely that tfpQ/Ip2 is also regulated by an activator in Moraxella. Primer extension assays with RNA isolated from Escherichia coli containing the subcloned pilin inversion region from M. lacunata showed that pivp is used for the expression of piv; however, tfpQ/Ip2 is not used for the transcription of tfpQ/I. 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Primer extension analyses were used to map the transcriptional start sites for the genes encoding the major pilin subunits (tfpQ/I) and the DNA invertase (piv), which determines pilin type expression. tfpQ/I transcription starts at a sigma 54-dependent promoter (tfpQ/Ip2) and, under certain growth conditions, this transcription is accompanied by weaker upstream transcription that starts at a potential sigma 70-dependent promoter (tfpQ/Ip1). piv is expressed in both M. lacunata and M. bovis from a putative sigma 70-dependent promoter (pivp) under all conditions assayed. sigma 54-dependent promoters require activators in order to initiate transcription; therefore, it is likely that tfpQ/Ip2 is also regulated by an activator in Moraxella. Primer extension assays with RNA isolated from Escherichia coli containing the subcloned pilin inversion region from M. lacunata showed that pivp is used for the expression of piv; however, tfpQ/Ip2 is not used for the transcription of tfpQ/I. Transcription from tfpQ/Ip2 was activated in E. coli when the sensor (PilS) and response regulator (PilR) proteins of type 4 pilin transcription in Pseudomonas aeruginosa were expressed from a plasmid. These results suggest that the expression of the type 4 pilin in M. lacunata and M. bovis is regulated not only by a site-specific DNA inversion system but also by a regulatory system which is functionally analogous to the PilS-PilR two-component system of P. aeruginosa</description><subject>Bacterial Outer Membrane Proteins - genetics</subject><subject>BACTERIAL PROTEINS</subject><subject>Bacterial Proteins - genetics</subject><subject>Bacteriology</subject><subject>Base Sequence</subject><subject>Deoxyribonucleic acid</subject><subject>DNA</subject><subject>DNA INVERTASE</subject><subject>DNA Nucleotidyltransferases - genetics</subject><subject>DNA-Binding Proteins</subject><subject>DNA-Directed RNA Polymerases - metabolism</subject><subject>ENZIMAS</subject><subject>ENZYME</subject><subject>ENZYMES</subject><subject>ESCHERICHIA COLI</subject><subject>Escherichia coli - genetics</subject><subject>Escherichia coli Proteins</subject><subject>EXPRESION GENICA</subject><subject>EXPRESSION DES GENES</subject><subject>FACTEUR DE TRANSCRIPTION</subject><subject>FACTORES DE TRANSCRIPCION</subject><subject>Fimbriae Proteins</subject><subject>GENE</subject><subject>GENE EXPRESSION</subject><subject>Gene Expression Regulation, Bacterial</subject><subject>GENES</subject><subject>GENETIC TRANSFORMATION</subject><subject>INITIATION</subject><subject>Integrases</subject><subject>INVERSION REGION</subject><subject>MICROBIAL PROTEINS</subject><subject>Molecular Sequence Data</subject><subject>MORAXELLA</subject><subject>Moraxella (Moraxella) bovis - genetics</subject><subject>Moraxella (Moraxella) bovis - growth &amp; development</subject><subject>Moraxella - genetics</subject><subject>Moraxella - growth &amp; development</subject><subject>PIV GENE</subject><subject>PIV PROMOTER</subject><subject>Promoter Regions, Genetic</subject><subject>PROMOTERS</subject><subject>PROTEINAS MICROBIANAS</subject><subject>PROTEINE MICROBIENNE</subject><subject>Pseudomonas aeruginosa - genetics</subject><subject>Recombinases</subject><subject>RNA Polymerase Sigma 54</subject><subject>Sigma Factor - metabolism</subject><subject>SIGMA FACTORS</subject><subject>SITE SPECIFIC DNA INVERSION</subject><subject>STRUCTURAL GENES</subject><subject>TFPQ/I GENES</subject><subject>TFPQ/I PROMOTER</subject><subject>TRANSCRIPCION</subject><subject>TRANSCRIPTION</subject><subject>TRANSCRIPTION FACTORS</subject><subject>Transcription Factors - genetics</subject><subject>Transcription, Genetic</subject><subject>TRANSCRIPTIONAL START SITE</subject><subject>TRANSFORMACION GENETICA</subject><subject>TRANSFORMATION GENETIQUE</subject><issn>0021-9193</issn><issn>1098-5530</issn><issn>1067-8832</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1997</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFks1u1DAUhS0EKsPAIyBZLFg1wT-JHS9YoIo_qYgF7dpynJuMR0kc7GRKn4DXxmlHHeiGlWX7fMf3-h6EMCU5pax6t69zKlXOeC6ZqjLJSZlTpeQTtKEkHZQlJ0_RhhBGM0UVf45exLgnhBZFyc7QmeKKC8U36PdVMGO0wU2z86PpcYBu6c26wb7F8-0EuMCT692IOxghYjM2eN4Bjm6GLE5gXetswqwfajeaCHe688QcznGivvlgfkHfG9wbu4xmNncWp-PaH1x8iZ61po_w6rhu0fWnj1cXX7LL75-_Xny4zGwpxZwJ0jbUKCUqUIZIArJSxFaNrYgA2zSMMSpKVpGq4K0kxhayLguugJdlzaziW_T-3nda6gEaC-McTK-n4AYTbrU3Tv97M7qd7vxBp-8WcuXfHvngfy4QZz24aNc-RvBL1FIVRZqD_K-QCiaISGVu0ZtHwr1fQhpF1IxJImkhRRJV9yIbfIwB2oeKKdFrIvS-XkvUjOs1EXpNhF4TkdDXf3f8AB4jcHp_57rdjQugTRwe2Z1MWuO16YKL-vrHap9a4EzxP8iXyG8</recordid><startdate>19971201</startdate><enddate>19971201</enddate><creator>Heinrich, D.W</creator><creator>Glasgow, A.C</creator><general>American Society for Microbiology</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>7QL</scope><scope>7TM</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>19971201</creationdate><title>Transcriptional regulation of type 4 pilin genes and the site-specific recombinase gene, piv, in Moraxella lacunata and Moraxella bovis</title><author>Heinrich, D.W ; Glasgow, A.C</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c576t-60fd1a9968e9a070e7890c8dc806ecdd222165280843f70ac47b5439e355b2c93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1997</creationdate><topic>Bacterial Outer Membrane Proteins - genetics</topic><topic>BACTERIAL PROTEINS</topic><topic>Bacterial Proteins - genetics</topic><topic>Bacteriology</topic><topic>Base Sequence</topic><topic>Deoxyribonucleic acid</topic><topic>DNA</topic><topic>DNA INVERTASE</topic><topic>DNA Nucleotidyltransferases - genetics</topic><topic>DNA-Binding Proteins</topic><topic>DNA-Directed RNA Polymerases - metabolism</topic><topic>ENZIMAS</topic><topic>ENZYME</topic><topic>ENZYMES</topic><topic>ESCHERICHIA COLI</topic><topic>Escherichia coli - genetics</topic><topic>Escherichia coli Proteins</topic><topic>EXPRESION GENICA</topic><topic>EXPRESSION DES GENES</topic><topic>FACTEUR DE TRANSCRIPTION</topic><topic>FACTORES DE TRANSCRIPCION</topic><topic>Fimbriae Proteins</topic><topic>GENE</topic><topic>GENE EXPRESSION</topic><topic>Gene Expression Regulation, Bacterial</topic><topic>GENES</topic><topic>GENETIC TRANSFORMATION</topic><topic>INITIATION</topic><topic>Integrases</topic><topic>INVERSION REGION</topic><topic>MICROBIAL PROTEINS</topic><topic>Molecular Sequence Data</topic><topic>MORAXELLA</topic><topic>Moraxella (Moraxella) bovis - genetics</topic><topic>Moraxella (Moraxella) bovis - growth &amp; development</topic><topic>Moraxella - genetics</topic><topic>Moraxella - growth &amp; development</topic><topic>PIV GENE</topic><topic>PIV PROMOTER</topic><topic>Promoter Regions, Genetic</topic><topic>PROMOTERS</topic><topic>PROTEINAS MICROBIANAS</topic><topic>PROTEINE MICROBIENNE</topic><topic>Pseudomonas aeruginosa - genetics</topic><topic>Recombinases</topic><topic>RNA Polymerase Sigma 54</topic><topic>Sigma Factor - metabolism</topic><topic>SIGMA FACTORS</topic><topic>SITE SPECIFIC DNA INVERSION</topic><topic>STRUCTURAL GENES</topic><topic>TFPQ/I GENES</topic><topic>TFPQ/I PROMOTER</topic><topic>TRANSCRIPCION</topic><topic>TRANSCRIPTION</topic><topic>TRANSCRIPTION FACTORS</topic><topic>Transcription Factors - genetics</topic><topic>Transcription, Genetic</topic><topic>TRANSCRIPTIONAL START SITE</topic><topic>TRANSFORMACION GENETICA</topic><topic>TRANSFORMATION GENETIQUE</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Heinrich, D.W</creatorcontrib><creatorcontrib>Glasgow, A.C</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>Bacteriology Abstracts (Microbiology B)</collection><collection>Nucleic Acids 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>Journal of Bacteriology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Heinrich, D.W</au><au>Glasgow, A.C</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Transcriptional regulation of type 4 pilin genes and the site-specific recombinase gene, piv, in Moraxella lacunata and Moraxella bovis</atitle><jtitle>Journal of Bacteriology</jtitle><addtitle>J Bacteriol</addtitle><date>1997-12-01</date><risdate>1997</risdate><volume>179</volume><issue>23</issue><spage>7298</spage><epage>7305</epage><pages>7298-7305</pages><issn>0021-9193</issn><eissn>1098-5530</eissn><eissn>1067-8832</eissn><coden>JOBAAY</coden><abstract>Moraxella lacunata and Moraxella bovis use type 4 pili to adhere to epithelial tissues of the cornea and conjunctiva. Primer extension analyses were used to map the transcriptional start sites for the genes encoding the major pilin subunits (tfpQ/I) and the DNA invertase (piv), which determines pilin type expression. tfpQ/I transcription starts at a sigma 54-dependent promoter (tfpQ/Ip2) and, under certain growth conditions, this transcription is accompanied by weaker upstream transcription that starts at a potential sigma 70-dependent promoter (tfpQ/Ip1). piv is expressed in both M. lacunata and M. bovis from a putative sigma 70-dependent promoter (pivp) under all conditions assayed. sigma 54-dependent promoters require activators in order to initiate transcription; therefore, it is likely that tfpQ/Ip2 is also regulated by an activator in Moraxella. Primer extension assays with RNA isolated from Escherichia coli containing the subcloned pilin inversion region from M. lacunata showed that pivp is used for the expression of piv; however, tfpQ/Ip2 is not used for the transcription of tfpQ/I. Transcription from tfpQ/Ip2 was activated in E. coli when the sensor (PilS) and response regulator (PilR) proteins of type 4 pilin transcription in Pseudomonas aeruginosa were expressed from a plasmid. These results suggest that the expression of the type 4 pilin in M. lacunata and M. bovis is regulated not only by a site-specific DNA inversion system but also by a regulatory system which is functionally analogous to the PilS-PilR two-component system of P. aeruginosa</abstract><cop>United States</cop><pub>American Society for Microbiology</pub><pmid>9393693</pmid><doi>10.1128/jb.179.23.7298-7305.1997</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record>
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subjects Bacterial Outer Membrane Proteins - genetics
BACTERIAL PROTEINS
Bacterial Proteins - genetics
Bacteriology
Base Sequence
Deoxyribonucleic acid
DNA
DNA INVERTASE
DNA Nucleotidyltransferases - genetics
DNA-Binding Proteins
DNA-Directed RNA Polymerases - metabolism
ENZIMAS
ENZYME
ENZYMES
ESCHERICHIA COLI
Escherichia coli - genetics
Escherichia coli Proteins
EXPRESION GENICA
EXPRESSION DES GENES
FACTEUR DE TRANSCRIPTION
FACTORES DE TRANSCRIPCION
Fimbriae Proteins
GENE
GENE EXPRESSION
Gene Expression Regulation, Bacterial
GENES
GENETIC TRANSFORMATION
INITIATION
Integrases
INVERSION REGION
MICROBIAL PROTEINS
Molecular Sequence Data
MORAXELLA
Moraxella (Moraxella) bovis - genetics
Moraxella (Moraxella) bovis - growth & development
Moraxella - genetics
Moraxella - growth & development
PIV GENE
PIV PROMOTER
Promoter Regions, Genetic
PROMOTERS
PROTEINAS MICROBIANAS
PROTEINE MICROBIENNE
Pseudomonas aeruginosa - genetics
Recombinases
RNA Polymerase Sigma 54
Sigma Factor - metabolism
SIGMA FACTORS
SITE SPECIFIC DNA INVERSION
STRUCTURAL GENES
TFPQ/I GENES
TFPQ/I PROMOTER
TRANSCRIPCION
TRANSCRIPTION
TRANSCRIPTION FACTORS
Transcription Factors - genetics
Transcription, Genetic
TRANSCRIPTIONAL START SITE
TRANSFORMACION GENETICA
TRANSFORMATION GENETIQUE
title Transcriptional regulation of type 4 pilin genes and the site-specific recombinase gene, piv, in Moraxella lacunata and Moraxella bovis
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