role for Lon protease in the control of the acid resistance genes of Escherichia coli
Lon protease is a major protease in cellular protein quality control, but also plays an important regulatory role by degrading various naturally unstable regulators. Here, we traced additional such regulators by identifying regulons with co-ordinately altered expression in a lon mutant by genome-wid...
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Veröffentlicht in: | Molecular microbiology 2008-07, Vol.69 (2), p.534-547 |
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description | Lon protease is a major protease in cellular protein quality control, but also plays an important regulatory role by degrading various naturally unstable regulators. Here, we traced additional such regulators by identifying regulons with co-ordinately altered expression in a lon mutant by genome-wide transcriptional profiling. Besides many members of the RcsA regulon (which validates our approach as RcsA is a known Lon substrate), many genes of the σS-dependent general stress response were upregulated in the lon mutant. However, the lon mutation did not affect σS levels nor σS activity in general, suggesting specific effects of Lon on secondary regulators involved in the control of subsets of σS-controlled genes. Lon-affected genes also included the major acid resistance genes (gadA, gadBC, gadE, hdeAB and hdeD), which led to the discovery that the essential acid resistance regulator GadE (whose expression is σS-controlled) is degraded in vivo in a Lon-dependent manner. GadE proteolysis is constitutive as it was observed even under conditions that induce the system (i.e. at low pH or during entry into stationary phase). GadE degradation was found to rapidly terminate the acid resistance response upon shift back to neutral pH and to avoid overexpression of acid resistance genes in stationary phase. |
doi_str_mv | 10.1111/j.1365-2958.2008.06306.x |
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Here, we traced additional such regulators by identifying regulons with co-ordinately altered expression in a lon mutant by genome-wide transcriptional profiling. Besides many members of the RcsA regulon (which validates our approach as RcsA is a known Lon substrate), many genes of the σS-dependent general stress response were upregulated in the lon mutant. However, the lon mutation did not affect σS levels nor σS activity in general, suggesting specific effects of Lon on secondary regulators involved in the control of subsets of σS-controlled genes. Lon-affected genes also included the major acid resistance genes (gadA, gadBC, gadE, hdeAB and hdeD), which led to the discovery that the essential acid resistance regulator GadE (whose expression is σS-controlled) is degraded in vivo in a Lon-dependent manner. GadE proteolysis is constitutive as it was observed even under conditions that induce the system (i.e. at low pH or during entry into stationary phase). GadE degradation was found to rapidly terminate the acid resistance response upon shift back to neutral pH and to avoid overexpression of acid resistance genes in stationary phase.</description><identifier>ISSN: 0950-382X</identifier><identifier>EISSN: 1365-2958</identifier><identifier>DOI: 10.1111/j.1365-2958.2008.06306.x</identifier><identifier>PMID: 18630346</identifier><language>eng</language><publisher>Oxford, UK: Oxford, UK : Blackwell Publishing Ltd</publisher><subject>Acids - toxicity ; Adaptation, Physiological ; Artificial Gene Fusion ; Bacterial proteins ; Bacterial Proteins - metabolism ; Bacteriology ; beta-Galactosidase - biosynthesis ; beta-Galactosidase - genetics ; Biological and medical sciences ; Drug resistance ; E coli ; Escherichia coli ; Escherichia coli - physiology ; Escherichia coli Proteins - metabolism ; Fundamental and applied biological sciences. Psychology ; Gene Deletion ; Gene expression ; Gene Expression Profiling ; Gene Expression Regulation, Bacterial ; Genes ; Genes, Reporter ; Genetics ; Microbiology ; Mutation ; Protease La - genetics ; Protease La - metabolism ; Proteases ; Regulon ; Sigma Factor - metabolism ; Transcription Factors - metabolism</subject><ispartof>Molecular microbiology, 2008-07, Vol.69 (2), p.534-547</ispartof><rights>2008 The Authors. Journal compilation © 2008 Blackwell Publishing Ltd</rights><rights>2008 INIST-CNRS</rights><rights>Copyright Blackwell Publishing Ltd. 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Here, we traced additional such regulators by identifying regulons with co-ordinately altered expression in a lon mutant by genome-wide transcriptional profiling. Besides many members of the RcsA regulon (which validates our approach as RcsA is a known Lon substrate), many genes of the σS-dependent general stress response were upregulated in the lon mutant. However, the lon mutation did not affect σS levels nor σS activity in general, suggesting specific effects of Lon on secondary regulators involved in the control of subsets of σS-controlled genes. Lon-affected genes also included the major acid resistance genes (gadA, gadBC, gadE, hdeAB and hdeD), which led to the discovery that the essential acid resistance regulator GadE (whose expression is σS-controlled) is degraded in vivo in a Lon-dependent manner. GadE proteolysis is constitutive as it was observed even under conditions that induce the system (i.e. at low pH or during entry into stationary phase). GadE degradation was found to rapidly terminate the acid resistance response upon shift back to neutral pH and to avoid overexpression of acid resistance genes in stationary phase.</description><subject>Acids - toxicity</subject><subject>Adaptation, Physiological</subject><subject>Artificial Gene Fusion</subject><subject>Bacterial proteins</subject><subject>Bacterial Proteins - metabolism</subject><subject>Bacteriology</subject><subject>beta-Galactosidase - biosynthesis</subject><subject>beta-Galactosidase - genetics</subject><subject>Biological and medical sciences</subject><subject>Drug resistance</subject><subject>E coli</subject><subject>Escherichia coli</subject><subject>Escherichia coli - physiology</subject><subject>Escherichia coli Proteins - metabolism</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Gene Deletion</subject><subject>Gene expression</subject><subject>Gene Expression Profiling</subject><subject>Gene Expression Regulation, Bacterial</subject><subject>Genes</subject><subject>Genes, Reporter</subject><subject>Genetics</subject><subject>Microbiology</subject><subject>Mutation</subject><subject>Protease La - genetics</subject><subject>Protease La - metabolism</subject><subject>Proteases</subject><subject>Regulon</subject><subject>Sigma Factor - metabolism</subject><subject>Transcription Factors - metabolism</subject><issn>0950-382X</issn><issn>1365-2958</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkUFvFCEUx4nR2LX6FZSY6G2mDxgYOHhomto22aYH28QbYZk3XTazQ4XZ2H57me6mJp7kAuT9_o-XH4RQBjUr62RTM6FkxY3UNQfQNSgBqn58RRYvhddkAUZCJTT_eUTe5bwBYIUSb8kR04UXjVqQuxQHpH1MdBlH-pDihC4jDSOd1kh9HKcC0Ng_X50PHU2YQ57c6JHe44h5Lp5nv8YU_Dq4khnCe_Kmd0PGD4f9mNx-P789u6yWNxdXZ6fLyjetUdVKGYbgOiEYSK-FVsgktIwJlL0A2aFizIsOWpSgG29a3mrHVyup-q6V4ph83bctc__aYZ7sNmSPw-BGjLtsORgwpmUF_PwPuIm7NJbRLDNKctVyKJDeQz7FnBP29iGFrUtPloGdtduNne3a2a6dtdtn7faxRD8e-u9WW-z-Bg-eC_DlALjs3dCn4i_kF45D0yqhm8J923O_w4BP_z2Avb6-mk8l_2mf71207j6VN-5-8PnfwTAhuRZ_ANRspK8</recordid><startdate>200807</startdate><enddate>200807</enddate><creator>Heuveling, Johanna</creator><creator>Possling, Alexandra</creator><creator>Hengge, Regine</creator><general>Oxford, UK : Blackwell Publishing Ltd</general><general>Blackwell Publishing Ltd</general><general>Blackwell Science</general><scope>FBQ</scope><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>7QP</scope><scope>7QR</scope><scope>7TK</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></search><sort><creationdate>200807</creationdate><title>role for Lon protease in the control of the acid resistance genes of Escherichia coli</title><author>Heuveling, Johanna ; Possling, Alexandra ; Hengge, Regine</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4796-b691e0ad33105c8386e1507113e5f305de611c3d07e5084c97278a2bb56fd753</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>Acids - toxicity</topic><topic>Adaptation, Physiological</topic><topic>Artificial Gene Fusion</topic><topic>Bacterial proteins</topic><topic>Bacterial Proteins - metabolism</topic><topic>Bacteriology</topic><topic>beta-Galactosidase - biosynthesis</topic><topic>beta-Galactosidase - genetics</topic><topic>Biological and medical sciences</topic><topic>Drug resistance</topic><topic>E coli</topic><topic>Escherichia coli</topic><topic>Escherichia coli - physiology</topic><topic>Escherichia coli Proteins - metabolism</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Gene Deletion</topic><topic>Gene expression</topic><topic>Gene Expression Profiling</topic><topic>Gene Expression Regulation, Bacterial</topic><topic>Genes</topic><topic>Genes, Reporter</topic><topic>Genetics</topic><topic>Microbiology</topic><topic>Mutation</topic><topic>Protease La - genetics</topic><topic>Protease La - metabolism</topic><topic>Proteases</topic><topic>Regulon</topic><topic>Sigma Factor - metabolism</topic><topic>Transcription Factors - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Heuveling, Johanna</creatorcontrib><creatorcontrib>Possling, Alexandra</creatorcontrib><creatorcontrib>Hengge, Regine</creatorcontrib><collection>AGRIS</collection><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>Calcium & Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Neurosciences Abstracts</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><jtitle>Molecular microbiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Heuveling, Johanna</au><au>Possling, Alexandra</au><au>Hengge, Regine</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>role for Lon protease in the control of the acid resistance genes of Escherichia coli</atitle><jtitle>Molecular microbiology</jtitle><addtitle>Mol Microbiol</addtitle><date>2008-07</date><risdate>2008</risdate><volume>69</volume><issue>2</issue><spage>534</spage><epage>547</epage><pages>534-547</pages><issn>0950-382X</issn><eissn>1365-2958</eissn><abstract>Lon protease is a major protease in cellular protein quality control, but also plays an important regulatory role by degrading various naturally unstable regulators. Here, we traced additional such regulators by identifying regulons with co-ordinately altered expression in a lon mutant by genome-wide transcriptional profiling. Besides many members of the RcsA regulon (which validates our approach as RcsA is a known Lon substrate), many genes of the σS-dependent general stress response were upregulated in the lon mutant. However, the lon mutation did not affect σS levels nor σS activity in general, suggesting specific effects of Lon on secondary regulators involved in the control of subsets of σS-controlled genes. Lon-affected genes also included the major acid resistance genes (gadA, gadBC, gadE, hdeAB and hdeD), which led to the discovery that the essential acid resistance regulator GadE (whose expression is σS-controlled) is degraded in vivo in a Lon-dependent manner. GadE proteolysis is constitutive as it was observed even under conditions that induce the system (i.e. at low pH or during entry into stationary phase). GadE degradation was found to rapidly terminate the acid resistance response upon shift back to neutral pH and to avoid overexpression of acid resistance genes in stationary phase.</abstract><cop>Oxford, UK</cop><pub>Oxford, UK : Blackwell Publishing Ltd</pub><pmid>18630346</pmid><doi>10.1111/j.1365-2958.2008.06306.x</doi><tpages>14</tpages></addata></record> |
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subjects | Acids - toxicity Adaptation, Physiological Artificial Gene Fusion Bacterial proteins Bacterial Proteins - metabolism Bacteriology beta-Galactosidase - biosynthesis beta-Galactosidase - genetics Biological and medical sciences Drug resistance E coli Escherichia coli Escherichia coli - physiology Escherichia coli Proteins - metabolism Fundamental and applied biological sciences. Psychology Gene Deletion Gene expression Gene Expression Profiling Gene Expression Regulation, Bacterial Genes Genes, Reporter Genetics Microbiology Mutation Protease La - genetics Protease La - metabolism Proteases Regulon Sigma Factor - metabolism Transcription Factors - metabolism |
title | role for Lon protease in the control of the acid resistance genes of Escherichia coli |
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