A physiological role for DNA supercoiling in the osmotic regulation of gene expression in S. typhimurium and E. coli
The proU locus encodes an osmotically inducible glycine betaine transport system that is important in the adaptation to osmotic stress. We present evidence that DNA supercoiling plays a key role in the osmotic induction of proU transcription. An increase in extracellular osmolarity increases in vivo...
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Veröffentlicht in: | Cell 1988-02, Vol.52 (4), p.569-584 |
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creator | Higgins, Christopher F. Dorman, Charles J. Stirling, Douglas A. Waddell, Lesley Booth, Ian R. May, Gerhard Bremer, Erhard |
description | The
proU locus encodes an osmotically inducible glycine betaine transport system that is important in the adaptation to osmotic stress. We present evidence that DNA supercoiling plays a key role in the osmotic induction of
proU transcription. An increase in extracellular osmolarity increases in vivo DNA supercoiling, and the expression of
proU is highly sensitive to these changes. Furthermore,
topA mutations can mimic an increase in osmolarity, facilitating
proU expression even in media of low osmolarity in which it is not normally expressed. Selection for
trans-acting mutations that affect
proU expression has yielded only mutations that alter DNA supercoiling, either in
topA or a new genetic locus,
osmZ, which strongly influences in vivo supercoiling. Mutations in
osmZ are highly pleiotropic, affecting expression of a variety of chromosomal genes including
ompF, ompC, fimA, and the
bgl operon, as well as increasing the frequency of site-specific DNA inversions that mediate fimbrial phase variation. |
doi_str_mv | 10.1016/0092-8674(88)90470-9 |
format | Article |
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proU locus encodes an osmotically inducible glycine betaine transport system that is important in the adaptation to osmotic stress. We present evidence that DNA supercoiling plays a key role in the osmotic induction of
proU transcription. An increase in extracellular osmolarity increases in vivo DNA supercoiling, and the expression of
proU is highly sensitive to these changes. Furthermore,
topA mutations can mimic an increase in osmolarity, facilitating
proU expression even in media of low osmolarity in which it is not normally expressed. Selection for
trans-acting mutations that affect
proU expression has yielded only mutations that alter DNA supercoiling, either in
topA or a new genetic locus,
osmZ, which strongly influences in vivo supercoiling. Mutations in
osmZ are highly pleiotropic, affecting expression of a variety of chromosomal genes including
ompF, ompC, fimA, and the
bgl operon, as well as increasing the frequency of site-specific DNA inversions that mediate fimbrial phase variation.</description><identifier>ISSN: 0092-8674</identifier><identifier>EISSN: 1097-4172</identifier><identifier>DOI: 10.1016/0092-8674(88)90470-9</identifier><identifier>PMID: 2830029</identifier><identifier>CODEN: CELLB5</identifier><language>eng</language><publisher>Cambridge, MA: Elsevier Inc</publisher><subject>Betaine - metabolism ; Biological and medical sciences ; Chromosome Mapping ; DNA Topoisomerases, Type I - genetics ; DNA Topoisomerases, Type II - physiology ; DNA, Bacterial - genetics ; DNA, Superhelical - genetics ; DNA-Directed RNA Polymerases - genetics ; Escherichia coli ; Escherichia coli - genetics ; Fundamental and applied biological sciences. Psychology ; Gene expression ; Gene Expression Regulation ; Genes, Bacterial ; Glucosides - metabolism ; Molecular and cellular biology ; Molecular genetics ; Potassium - physiology ; Promoter Regions, Genetic ; Recombination, Genetic ; Salmonella typhimurium ; Salmonella typhimurium - genetics ; Transcription, Genetic ; Water-Electrolyte Balance</subject><ispartof>Cell, 1988-02, Vol.52 (4), p.569-584</ispartof><rights>1988</rights><rights>1988 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c332t-3497a37372b7ff392b3216b5bd65910bcde8cc324d6e7ca563ccc1de1bece7653</citedby><cites>FETCH-LOGICAL-c332t-3497a37372b7ff392b3216b5bd65910bcde8cc324d6e7ca563ccc1de1bece7653</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/0092-8674(88)90470-9$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>315,781,785,3551,27926,27927,45997</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=7587838$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/2830029$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Higgins, Christopher F.</creatorcontrib><creatorcontrib>Dorman, Charles J.</creatorcontrib><creatorcontrib>Stirling, Douglas A.</creatorcontrib><creatorcontrib>Waddell, Lesley</creatorcontrib><creatorcontrib>Booth, Ian R.</creatorcontrib><creatorcontrib>May, Gerhard</creatorcontrib><creatorcontrib>Bremer, Erhard</creatorcontrib><title>A physiological role for DNA supercoiling in the osmotic regulation of gene expression in S. typhimurium and E. coli</title><title>Cell</title><addtitle>Cell</addtitle><description>The
proU locus encodes an osmotically inducible glycine betaine transport system that is important in the adaptation to osmotic stress. We present evidence that DNA supercoiling plays a key role in the osmotic induction of
proU transcription. An increase in extracellular osmolarity increases in vivo DNA supercoiling, and the expression of
proU is highly sensitive to these changes. Furthermore,
topA mutations can mimic an increase in osmolarity, facilitating
proU expression even in media of low osmolarity in which it is not normally expressed. Selection for
trans-acting mutations that affect
proU expression has yielded only mutations that alter DNA supercoiling, either in
topA or a new genetic locus,
osmZ, which strongly influences in vivo supercoiling. Mutations in
osmZ are highly pleiotropic, affecting expression of a variety of chromosomal genes including
ompF, ompC, fimA, and the
bgl operon, as well as increasing the frequency of site-specific DNA inversions that mediate fimbrial phase variation.</description><subject>Betaine - metabolism</subject><subject>Biological and medical sciences</subject><subject>Chromosome Mapping</subject><subject>DNA Topoisomerases, Type I - genetics</subject><subject>DNA Topoisomerases, Type II - physiology</subject><subject>DNA, Bacterial - genetics</subject><subject>DNA, Superhelical - genetics</subject><subject>DNA-Directed RNA Polymerases - genetics</subject><subject>Escherichia coli</subject><subject>Escherichia coli - genetics</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Gene expression</subject><subject>Gene Expression Regulation</subject><subject>Genes, Bacterial</subject><subject>Glucosides - metabolism</subject><subject>Molecular and cellular biology</subject><subject>Molecular genetics</subject><subject>Potassium - physiology</subject><subject>Promoter Regions, Genetic</subject><subject>Recombination, Genetic</subject><subject>Salmonella typhimurium</subject><subject>Salmonella typhimurium - genetics</subject><subject>Transcription, Genetic</subject><subject>Water-Electrolyte Balance</subject><issn>0092-8674</issn><issn>1097-4172</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1988</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkUuP1DAQhC0EWoaFfwCSDwjBIYMfcWxfVhoty0NawQE4W06nM2OUxMFOEPPvSZjRHOHUUvdXpVYVIc8523LGq7eMWVGYSpevjXljWalZYR-QDWdWFyXX4iHZXJDH5EnOPxhjRil1Ra6EkYwJuyHTjo6HYw6xi_sAvqMpdkjbmOi7zzua5xETxNCFYU_DQKcD0pj7OAWgCfdz56cQBxpbuscBKf4eE-a8rhb465ZOx_EQ-jmFuad-aOjdlkLswlPyqPVdxmfneU2-v7_7dvuxuP_y4dPt7r4AKcVUyNJqL7XUotZtK62opeBVreqmUpazGho0AFKUTYUavKokAPAGeY2AulLymrw6-Y4p_pwxT64PGbDr_IBxzk4bzqSpxH9Brpi2Uq6O5QmEFHNO2Loxhd6no-PMra24NXK3Ru6McX9bcXaRvTj7z3WPzUV0rmG5vzzffV5KaJMfIOQLppXRRpoFuzlhuIT2K2ByGQIOgE1ICJNrYvj3H38A79apMg</recordid><startdate>19880226</startdate><enddate>19880226</enddate><creator>Higgins, Christopher F.</creator><creator>Dorman, Charles J.</creator><creator>Stirling, Douglas A.</creator><creator>Waddell, Lesley</creator><creator>Booth, Ian R.</creator><creator>May, Gerhard</creator><creator>Bremer, Erhard</creator><general>Elsevier Inc</general><general>Cell Press</general><scope>IQODW</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>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope></search><sort><creationdate>19880226</creationdate><title>A physiological role for DNA supercoiling in the osmotic regulation of gene expression in S. typhimurium and E. coli</title><author>Higgins, Christopher F. ; Dorman, Charles J. ; Stirling, Douglas A. ; Waddell, Lesley ; Booth, Ian R. ; May, Gerhard ; Bremer, Erhard</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c332t-3497a37372b7ff392b3216b5bd65910bcde8cc324d6e7ca563ccc1de1bece7653</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1988</creationdate><topic>Betaine - metabolism</topic><topic>Biological and medical sciences</topic><topic>Chromosome Mapping</topic><topic>DNA Topoisomerases, Type I - genetics</topic><topic>DNA Topoisomerases, Type II - physiology</topic><topic>DNA, Bacterial - genetics</topic><topic>DNA, Superhelical - genetics</topic><topic>DNA-Directed RNA Polymerases - genetics</topic><topic>Escherichia coli</topic><topic>Escherichia coli - genetics</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Gene expression</topic><topic>Gene Expression Regulation</topic><topic>Genes, Bacterial</topic><topic>Glucosides - metabolism</topic><topic>Molecular and cellular biology</topic><topic>Molecular genetics</topic><topic>Potassium - physiology</topic><topic>Promoter Regions, Genetic</topic><topic>Recombination, Genetic</topic><topic>Salmonella typhimurium</topic><topic>Salmonella typhimurium - genetics</topic><topic>Transcription, Genetic</topic><topic>Water-Electrolyte Balance</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Higgins, Christopher F.</creatorcontrib><creatorcontrib>Dorman, Charles J.</creatorcontrib><creatorcontrib>Stirling, Douglas A.</creatorcontrib><creatorcontrib>Waddell, Lesley</creatorcontrib><creatorcontrib>Booth, Ian R.</creatorcontrib><creatorcontrib>May, Gerhard</creatorcontrib><creatorcontrib>Bremer, Erhard</creatorcontrib><collection>Pascal-Francis</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>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Cell</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Higgins, Christopher F.</au><au>Dorman, Charles J.</au><au>Stirling, Douglas A.</au><au>Waddell, Lesley</au><au>Booth, Ian R.</au><au>May, Gerhard</au><au>Bremer, Erhard</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A physiological role for DNA supercoiling in the osmotic regulation of gene expression in S. typhimurium and E. coli</atitle><jtitle>Cell</jtitle><addtitle>Cell</addtitle><date>1988-02-26</date><risdate>1988</risdate><volume>52</volume><issue>4</issue><spage>569</spage><epage>584</epage><pages>569-584</pages><issn>0092-8674</issn><eissn>1097-4172</eissn><coden>CELLB5</coden><abstract>The
proU locus encodes an osmotically inducible glycine betaine transport system that is important in the adaptation to osmotic stress. We present evidence that DNA supercoiling plays a key role in the osmotic induction of
proU transcription. An increase in extracellular osmolarity increases in vivo DNA supercoiling, and the expression of
proU is highly sensitive to these changes. Furthermore,
topA mutations can mimic an increase in osmolarity, facilitating
proU expression even in media of low osmolarity in which it is not normally expressed. Selection for
trans-acting mutations that affect
proU expression has yielded only mutations that alter DNA supercoiling, either in
topA or a new genetic locus,
osmZ, which strongly influences in vivo supercoiling. Mutations in
osmZ are highly pleiotropic, affecting expression of a variety of chromosomal genes including
ompF, ompC, fimA, and the
bgl operon, as well as increasing the frequency of site-specific DNA inversions that mediate fimbrial phase variation.</abstract><cop>Cambridge, MA</cop><pub>Elsevier Inc</pub><pmid>2830029</pmid><doi>10.1016/0092-8674(88)90470-9</doi><tpages>16</tpages></addata></record> |
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subjects | Betaine - metabolism Biological and medical sciences Chromosome Mapping DNA Topoisomerases, Type I - genetics DNA Topoisomerases, Type II - physiology DNA, Bacterial - genetics DNA, Superhelical - genetics DNA-Directed RNA Polymerases - genetics Escherichia coli Escherichia coli - genetics Fundamental and applied biological sciences. Psychology Gene expression Gene Expression Regulation Genes, Bacterial Glucosides - metabolism Molecular and cellular biology Molecular genetics Potassium - physiology Promoter Regions, Genetic Recombination, Genetic Salmonella typhimurium Salmonella typhimurium - genetics Transcription, Genetic Water-Electrolyte Balance |
title | A physiological role for DNA supercoiling in the osmotic regulation of gene expression in S. typhimurium and E. coli |
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