Loading…

FIS activates glnAp2 in Escherichia coli: role of a DNA bend centered at −55, upstream of the transcription start site

Abstract A binding site for the Escherichia coli nucleoid binding protein FIS (factor for inversion stimulation) was identified upstream of a σ54-dependent promoter, glnAp2. The binding and bending center of FIS is positioned at −55 with respect to the transcription start site (+1). Binding of FIS a...

Full description

Saved in:
Bibliographic Details
Published in:FEMS microbiology letters 2006-04, Vol.257 (1), p.99-105
Main Authors: Huo, Yi-Xin, Nan, Bei-Yan, You, Cong-Hui, Tian, Zhe-Xian, Kolb, Annie, Wang, Yi-Ping
Format: Article
Language:English
Subjects:
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by
cites
container_end_page 105
container_issue 1
container_start_page 99
container_title FEMS microbiology letters
container_volume 257
creator Huo, Yi-Xin
Nan, Bei-Yan
You, Cong-Hui
Tian, Zhe-Xian
Kolb, Annie
Wang, Yi-Ping
description Abstract A binding site for the Escherichia coli nucleoid binding protein FIS (factor for inversion stimulation) was identified upstream of a σ54-dependent promoter, glnAp2. The binding and bending center of FIS is positioned at −55 with respect to the transcription start site (+1). Binding of FIS at this site activates the transcription of glnAp2 both in vivo and in vitro. Furthermore, we substituted the FIS-mediated DNA bending with other protein (cAMP receptor protein or integration host factor)-mediated DNA bending, without changing the position of the bending center. In vitro transcription assays indicated that all DNA bends centered at −55 activate transcriptional initiation of glnAp2, especially when linear templates were used.
doi_str_mv 10.1111/j.1574-6968.2006.00150.x
format article
fullrecord <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_proquest_miscellaneous_67774220</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><oup_id>10.1111/j.1574-6968.2006.00150.x</oup_id><sourcerecordid>67774220</sourcerecordid><originalsourceid>FETCH-LOGICAL-o3640-391b521308628ede181b677430d7c52659fdf122022a91d29b18f2c2474fa1e93</originalsourceid><addsrcrecordid>eNp1kc-O0zAQhy0EYsvCKyBLCE4kjO34TxCXatnCSgUOwNlyHYe6SpNgO9B9A848Ik-CQwsrgfBlLM33G9nzIYQJlCSfZ7uScFkVohaqpACiBCAcysMttPjTuI0WwKQqCNTyDN2LcQcAFQVxF50RwTlTTC3QYXX1Hhub_BeTXMSfun45Uux7fBnt1gVvt95gO3T-OQ5D5_DQYoNfvl3ijesbbF2fXHANNgn_-Pad86d4GmMKzuxnMm0dTsH00QY_Jj_0OCYTEo4-ufvoTmu66B6c6jn6uLr8cPG6WL97dXWxXBcDExUUrCYbTgkDJahyjSOKbISUFYNGWk4Fr9umJZQCpaYmDa03RLXU0kpWrSGuZufoyXHuGIbPk4tJ7320rutM74Yp6jxMVjmfwUd_gbthCn1-m6YMBBdESZWphydq2uxdo8fg9yZc698bzcDjE2CiNV2bv299vOEkr2kFM_fiyH31nbu-6YOeDeudnkXqWaSeDetfhvVBr96s8yXH2TE-TON_wsU_YfYTVYWliw</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2306561878</pqid></control><display><type>article</type><title>FIS activates glnAp2 in Escherichia coli: role of a DNA bend centered at −55, upstream of the transcription start site</title><source>Oxford Journals Online</source><creator>Huo, Yi-Xin ; Nan, Bei-Yan ; You, Cong-Hui ; Tian, Zhe-Xian ; Kolb, Annie ; Wang, Yi-Ping</creator><creatorcontrib>Huo, Yi-Xin ; Nan, Bei-Yan ; You, Cong-Hui ; Tian, Zhe-Xian ; Kolb, Annie ; Wang, Yi-Ping</creatorcontrib><description>Abstract A binding site for the Escherichia coli nucleoid binding protein FIS (factor for inversion stimulation) was identified upstream of a σ54-dependent promoter, glnAp2. The binding and bending center of FIS is positioned at −55 with respect to the transcription start site (+1). Binding of FIS at this site activates the transcription of glnAp2 both in vivo and in vitro. Furthermore, we substituted the FIS-mediated DNA bending with other protein (cAMP receptor protein or integration host factor)-mediated DNA bending, without changing the position of the bending center. In vitro transcription assays indicated that all DNA bends centered at −55 activate transcriptional initiation of glnAp2, especially when linear templates were used.</description><identifier>ISSN: 0378-1097</identifier><identifier>EISSN: 1574-6968</identifier><identifier>DOI: 10.1111/j.1574-6968.2006.00150.x</identifier><identifier>PMID: 16553838</identifier><identifier>CODEN: FMLED7</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Publishing Ltd</publisher><subject>Bacteria ; Bacteriology ; Base Sequence ; Bending ; Bends ; Binding sites ; Biological and medical sciences ; cAMP receptor protein (CRP) ; Deoxyribonucleic acid ; DNA ; DNA, Bacterial - chemistry ; DNA, Bacterial - genetics ; DNA, Bacterial - metabolism ; E coli ; Enhancer Elements, Genetic ; Escherichia coli ; Escherichia coli - genetics ; Escherichia coli - metabolism ; Escherichia coli Proteins - genetics ; Escherichia coli Proteins - metabolism ; factor for inversion stimulation (FIS) ; Factor For Inversion Stimulation Protein - genetics ; Factor For Inversion Stimulation Protein - metabolism ; Fundamental and applied biological sciences. Psychology ; Gene Expression Regulation, Bacterial ; Genetics ; Glutamate-Ammonia Ligase - chemistry ; Glutamate-Ammonia Ligase - genetics ; Glutamate-Ammonia Ligase - metabolism ; Integration host factor ; integration host factor (IHF) ; Metabolism. Enzymes ; Microbiology ; Molecular Sequence Data ; Nucleic Acid Conformation ; Promoter Regions, Genetic ; Proteins ; protein‐mediated DNA bending ; Transcription initiation ; Transcription, Genetic ; σ54‐RNA polymerase (Eσ54)</subject><ispartof>FEMS microbiology letters, 2006-04, Vol.257 (1), p.99-105</ispartof><rights>2006 Federation of European Microbiological Societies 2006</rights><rights>2006 INIST-CNRS</rights><rights>2006 Federation of European Microbiological Societies</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=17592408$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16553838$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Huo, Yi-Xin</creatorcontrib><creatorcontrib>Nan, Bei-Yan</creatorcontrib><creatorcontrib>You, Cong-Hui</creatorcontrib><creatorcontrib>Tian, Zhe-Xian</creatorcontrib><creatorcontrib>Kolb, Annie</creatorcontrib><creatorcontrib>Wang, Yi-Ping</creatorcontrib><title>FIS activates glnAp2 in Escherichia coli: role of a DNA bend centered at −55, upstream of the transcription start site</title><title>FEMS microbiology letters</title><addtitle>FEMS Microbiol Lett</addtitle><description>Abstract A binding site for the Escherichia coli nucleoid binding protein FIS (factor for inversion stimulation) was identified upstream of a σ54-dependent promoter, glnAp2. The binding and bending center of FIS is positioned at −55 with respect to the transcription start site (+1). Binding of FIS at this site activates the transcription of glnAp2 both in vivo and in vitro. Furthermore, we substituted the FIS-mediated DNA bending with other protein (cAMP receptor protein or integration host factor)-mediated DNA bending, without changing the position of the bending center. In vitro transcription assays indicated that all DNA bends centered at −55 activate transcriptional initiation of glnAp2, especially when linear templates were used.</description><subject>Bacteria</subject><subject>Bacteriology</subject><subject>Base Sequence</subject><subject>Bending</subject><subject>Bends</subject><subject>Binding sites</subject><subject>Biological and medical sciences</subject><subject>cAMP receptor protein (CRP)</subject><subject>Deoxyribonucleic acid</subject><subject>DNA</subject><subject>DNA, Bacterial - chemistry</subject><subject>DNA, Bacterial - genetics</subject><subject>DNA, Bacterial - metabolism</subject><subject>E coli</subject><subject>Enhancer Elements, Genetic</subject><subject>Escherichia coli</subject><subject>Escherichia coli - genetics</subject><subject>Escherichia coli - metabolism</subject><subject>Escherichia coli Proteins - genetics</subject><subject>Escherichia coli Proteins - metabolism</subject><subject>factor for inversion stimulation (FIS)</subject><subject>Factor For Inversion Stimulation Protein - genetics</subject><subject>Factor For Inversion Stimulation Protein - metabolism</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Gene Expression Regulation, Bacterial</subject><subject>Genetics</subject><subject>Glutamate-Ammonia Ligase - chemistry</subject><subject>Glutamate-Ammonia Ligase - genetics</subject><subject>Glutamate-Ammonia Ligase - metabolism</subject><subject>Integration host factor</subject><subject>integration host factor (IHF)</subject><subject>Metabolism. Enzymes</subject><subject>Microbiology</subject><subject>Molecular Sequence Data</subject><subject>Nucleic Acid Conformation</subject><subject>Promoter Regions, Genetic</subject><subject>Proteins</subject><subject>protein‐mediated DNA bending</subject><subject>Transcription initiation</subject><subject>Transcription, Genetic</subject><subject>σ54‐RNA polymerase (Eσ54)</subject><issn>0378-1097</issn><issn>1574-6968</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2006</creationdate><recordtype>article</recordtype><recordid>eNp1kc-O0zAQhy0EYsvCKyBLCE4kjO34TxCXatnCSgUOwNlyHYe6SpNgO9B9A848Ik-CQwsrgfBlLM33G9nzIYQJlCSfZ7uScFkVohaqpACiBCAcysMttPjTuI0WwKQqCNTyDN2LcQcAFQVxF50RwTlTTC3QYXX1Hhub_BeTXMSfun45Uux7fBnt1gVvt95gO3T-OQ5D5_DQYoNfvl3ijesbbF2fXHANNgn_-Pad86d4GmMKzuxnMm0dTsH00QY_Jj_0OCYTEo4-ufvoTmu66B6c6jn6uLr8cPG6WL97dXWxXBcDExUUrCYbTgkDJahyjSOKbISUFYNGWk4Fr9umJZQCpaYmDa03RLXU0kpWrSGuZufoyXHuGIbPk4tJ7320rutM74Yp6jxMVjmfwUd_gbthCn1-m6YMBBdESZWphydq2uxdo8fg9yZc698bzcDjE2CiNV2bv299vOEkr2kFM_fiyH31nbu-6YOeDeudnkXqWaSeDetfhvVBr96s8yXH2TE-TON_wsU_YfYTVYWliw</recordid><startdate>200604</startdate><enddate>200604</enddate><creator>Huo, Yi-Xin</creator><creator>Nan, Bei-Yan</creator><creator>You, Cong-Hui</creator><creator>Tian, Zhe-Xian</creator><creator>Kolb, Annie</creator><creator>Wang, Yi-Ping</creator><general>Blackwell Publishing Ltd</general><general>Blackwell</general><general>Oxford University Press</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>3V.</scope><scope>7QL</scope><scope>7T7</scope><scope>7TK</scope><scope>7TM</scope><scope>7U9</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7N</scope><scope>M7P</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>RC3</scope><scope>7X8</scope></search><sort><creationdate>200604</creationdate><title>FIS activates glnAp2 in Escherichia coli: role of a DNA bend centered at −55, upstream of the transcription start site</title><author>Huo, Yi-Xin ; Nan, Bei-Yan ; You, Cong-Hui ; Tian, Zhe-Xian ; Kolb, Annie ; Wang, Yi-Ping</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-o3640-391b521308628ede181b677430d7c52659fdf122022a91d29b18f2c2474fa1e93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2006</creationdate><topic>Bacteria</topic><topic>Bacteriology</topic><topic>Base Sequence</topic><topic>Bending</topic><topic>Bends</topic><topic>Binding sites</topic><topic>Biological and medical sciences</topic><topic>cAMP receptor protein (CRP)</topic><topic>Deoxyribonucleic acid</topic><topic>DNA</topic><topic>DNA, Bacterial - chemistry</topic><topic>DNA, Bacterial - genetics</topic><topic>DNA, Bacterial - metabolism</topic><topic>E coli</topic><topic>Enhancer Elements, Genetic</topic><topic>Escherichia coli</topic><topic>Escherichia coli - genetics</topic><topic>Escherichia coli - metabolism</topic><topic>Escherichia coli Proteins - genetics</topic><topic>Escherichia coli Proteins - metabolism</topic><topic>factor for inversion stimulation (FIS)</topic><topic>Factor For Inversion Stimulation Protein - genetics</topic><topic>Factor For Inversion Stimulation Protein - metabolism</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Gene Expression Regulation, Bacterial</topic><topic>Genetics</topic><topic>Glutamate-Ammonia Ligase - chemistry</topic><topic>Glutamate-Ammonia Ligase - genetics</topic><topic>Glutamate-Ammonia Ligase - metabolism</topic><topic>Integration host factor</topic><topic>integration host factor (IHF)</topic><topic>Metabolism. Enzymes</topic><topic>Microbiology</topic><topic>Molecular Sequence Data</topic><topic>Nucleic Acid Conformation</topic><topic>Promoter Regions, Genetic</topic><topic>Proteins</topic><topic>protein‐mediated DNA bending</topic><topic>Transcription initiation</topic><topic>Transcription, Genetic</topic><topic>σ54‐RNA polymerase (Eσ54)</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Huo, Yi-Xin</creatorcontrib><creatorcontrib>Nan, Bei-Yan</creatorcontrib><creatorcontrib>You, Cong-Hui</creatorcontrib><creatorcontrib>Tian, Zhe-Xian</creatorcontrib><creatorcontrib>Kolb, Annie</creatorcontrib><creatorcontrib>Wang, Yi-Ping</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>ProQuest Central (Corporate)</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>ProQuest Health &amp; Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Public Health Database</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest One Sustainability</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>AUTh Library subscriptions: ProQuest Central</collection><collection>ProQuest Natural Science Collection</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Biological Sciences</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biological Science Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>FEMS microbiology letters</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Huo, Yi-Xin</au><au>Nan, Bei-Yan</au><au>You, Cong-Hui</au><au>Tian, Zhe-Xian</au><au>Kolb, Annie</au><au>Wang, Yi-Ping</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>FIS activates glnAp2 in Escherichia coli: role of a DNA bend centered at −55, upstream of the transcription start site</atitle><jtitle>FEMS microbiology letters</jtitle><addtitle>FEMS Microbiol Lett</addtitle><date>2006-04</date><risdate>2006</risdate><volume>257</volume><issue>1</issue><spage>99</spage><epage>105</epage><pages>99-105</pages><issn>0378-1097</issn><eissn>1574-6968</eissn><coden>FMLED7</coden><abstract>Abstract A binding site for the Escherichia coli nucleoid binding protein FIS (factor for inversion stimulation) was identified upstream of a σ54-dependent promoter, glnAp2. The binding and bending center of FIS is positioned at −55 with respect to the transcription start site (+1). Binding of FIS at this site activates the transcription of glnAp2 both in vivo and in vitro. Furthermore, we substituted the FIS-mediated DNA bending with other protein (cAMP receptor protein or integration host factor)-mediated DNA bending, without changing the position of the bending center. In vitro transcription assays indicated that all DNA bends centered at −55 activate transcriptional initiation of glnAp2, especially when linear templates were used.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>16553838</pmid><doi>10.1111/j.1574-6968.2006.00150.x</doi><tpages>7</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0378-1097
ispartof FEMS microbiology letters, 2006-04, Vol.257 (1), p.99-105
issn 0378-1097
1574-6968
language eng
recordid cdi_proquest_miscellaneous_67774220
source Oxford Journals Online
subjects Bacteria
Bacteriology
Base Sequence
Bending
Bends
Binding sites
Biological and medical sciences
cAMP receptor protein (CRP)
Deoxyribonucleic acid
DNA
DNA, Bacterial - chemistry
DNA, Bacterial - genetics
DNA, Bacterial - metabolism
E coli
Enhancer Elements, Genetic
Escherichia coli
Escherichia coli - genetics
Escherichia coli - metabolism
Escherichia coli Proteins - genetics
Escherichia coli Proteins - metabolism
factor for inversion stimulation (FIS)
Factor For Inversion Stimulation Protein - genetics
Factor For Inversion Stimulation Protein - metabolism
Fundamental and applied biological sciences. Psychology
Gene Expression Regulation, Bacterial
Genetics
Glutamate-Ammonia Ligase - chemistry
Glutamate-Ammonia Ligase - genetics
Glutamate-Ammonia Ligase - metabolism
Integration host factor
integration host factor (IHF)
Metabolism. Enzymes
Microbiology
Molecular Sequence Data
Nucleic Acid Conformation
Promoter Regions, Genetic
Proteins
protein‐mediated DNA bending
Transcription initiation
Transcription, Genetic
σ54‐RNA polymerase (Eσ54)
title FIS activates glnAp2 in Escherichia coli: role of a DNA bend centered at −55, upstream of the transcription start site
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-07T20%3A53%3A24IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=FIS%20activates%20glnAp2%20in%20Escherichia%20coli:%20role%20of%20a%20DNA%20bend%20centered%20at%20%E2%88%9255,%20upstream%20of%20the%20transcription%20start%20site&rft.jtitle=FEMS%20microbiology%20letters&rft.au=Huo,%20Yi-Xin&rft.date=2006-04&rft.volume=257&rft.issue=1&rft.spage=99&rft.epage=105&rft.pages=99-105&rft.issn=0378-1097&rft.eissn=1574-6968&rft.coden=FMLED7&rft_id=info:doi/10.1111/j.1574-6968.2006.00150.x&rft_dat=%3Cproquest_pubme%3E67774220%3C/proquest_pubme%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-o3640-391b521308628ede181b677430d7c52659fdf122022a91d29b18f2c2474fa1e93%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=2306561878&rft_id=info:pmid/16553838&rft_oup_id=10.1111/j.1574-6968.2006.00150.x&rfr_iscdi=true