Expression of phage P4 integrase is regulated negatively by both Int and Vis
Dipartimento di Scienze Biomolecolari e Biotecnologie, Università degli Studi di Milano, Via Celoria 26, 20133 Milano, Italy Correspondence D. Ghisotti Daniela.Ghisotti{at}unimi.it Phage P4 int gene encodes the integrase responsible for phage integration into and excision from the Escherichia coli c...
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creator | Piazzolla, D Cali, S Spoldi, E Forti, F Sala, C Magnoni, F Deho, G Ghisotti, D |
description | Dipartimento di Scienze Biomolecolari e Biotecnologie, Università degli Studi di Milano, Via Celoria 26, 20133 Milano, Italy
Correspondence D. Ghisotti Daniela.Ghisotti{at}unimi.it
Phage P4 int gene encodes the integrase responsible for phage integration into and excision from the Escherichia coli chromosome. Here, the data showing that P4 int expression is regulated in a complex manner at different levels are presented. First of all, the P int promoter is regulated negatively by both Int and Vis, the P4 excisionase. The N-terminal portion of Int appears to be sufficient for such a negative autoregulation, suggesting that the Int N terminus is implicated in DNA binding. Second, full-length transcripts covering the entire int gene could be detected only upon P4 infection, whereas in P4 lysogens only short 5'-end covering transcripts were detectable. On the other hand, transcripts covering the 5'-end of int were also very abundant upon infection. It thus appears that premature transcription termination and/or mRNA degradation play a role in Int-negative regulation both on the basal prophage transcription and upon infection. Finally, comparison between P int lacZ transcriptional and translational fusions suggests that Vis regulates Int expression post-transcriptionally. The findings that Vis is also an RNA-binding protein and that Int may be translated from two different start codons have implications on possible regulation models of Int expression.
Present address: Max F. Perutz Laboratories at the Vienna Biocenter, Department of Microbiology and Genetics, University of Vienna, 1030 Vienna, Austria.
Present address: Keryos, Via della Filanda 5, 20060 Gessate (MI), Italy.
Present address: Molmed SpA, Via Olgettina 58, 20132 Milano, Italy. |
doi_str_mv | 10.1099/vir.0.81875-0 |
format | Article |
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Correspondence D. Ghisotti Daniela.Ghisotti{at}unimi.it
Phage P4 int gene encodes the integrase responsible for phage integration into and excision from the Escherichia coli chromosome. Here, the data showing that P4 int expression is regulated in a complex manner at different levels are presented. First of all, the P int promoter is regulated negatively by both Int and Vis, the P4 excisionase. The N-terminal portion of Int appears to be sufficient for such a negative autoregulation, suggesting that the Int N terminus is implicated in DNA binding. Second, full-length transcripts covering the entire int gene could be detected only upon P4 infection, whereas in P4 lysogens only short 5'-end covering transcripts were detectable. On the other hand, transcripts covering the 5'-end of int were also very abundant upon infection. It thus appears that premature transcription termination and/or mRNA degradation play a role in Int-negative regulation both on the basal prophage transcription and upon infection. Finally, comparison between P int lacZ transcriptional and translational fusions suggests that Vis regulates Int expression post-transcriptionally. The findings that Vis is also an RNA-binding protein and that Int may be translated from two different start codons have implications on possible regulation models of Int expression.
Present address: Max F. Perutz Laboratories at the Vienna Biocenter, Department of Microbiology and Genetics, University of Vienna, 1030 Vienna, Austria.
Present address: Keryos, Via della Filanda 5, 20060 Gessate (MI), Italy.
Present address: Molmed SpA, Via Olgettina 58, 20132 Milano, Italy.</description><identifier>ISSN: 0022-1317</identifier><identifier>EISSN: 1465-2099</identifier><identifier>DOI: 10.1099/vir.0.81875-0</identifier><identifier>PMID: 16847139</identifier><identifier>CODEN: JGVIAY</identifier><language>eng</language><publisher>Reading: Soc General Microbiol</publisher><subject>Artificial Gene Fusion ; Attachment Sites, Microbiological ; Base Sequence ; beta-Galactosidase - analysis ; beta-Galactosidase - genetics ; Biological and medical sciences ; Coliphages - enzymology ; Coliphages - genetics ; DNA-Binding Proteins - biosynthesis ; DNA-Binding Proteins - genetics ; DNA-Binding Proteins - physiology ; Escherichia coli ; Escherichia coli - genetics ; Escherichia coli - virology ; Fundamental and applied biological sciences. Psychology ; Gene Expression Regulation, Viral ; Genes, Reporter ; Integrases - biosynthesis ; Integrases - genetics ; Microbiology ; Miscellaneous ; Molecular Sequence Data ; Phage P4 ; Protein Binding ; Protein Structure, Tertiary ; RNA, Messenger - analysis ; RNA, Viral - analysis ; Viral Proteins - physiology ; Virology</subject><ispartof>Journal of general virology, 2006-08, Vol.87 (8), p.2423-2431</ispartof><rights>2006 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c490t-2003907f37c0788200d15201b14c2ebd8d8e5932e780ac22e30b0c408a1572f53</citedby><cites>FETCH-LOGICAL-c490t-2003907f37c0788200d15201b14c2ebd8d8e5932e780ac22e30b0c408a1572f53</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,3733,3734,27903,27904</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=17986540$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16847139$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Piazzolla, D</creatorcontrib><creatorcontrib>Cali, S</creatorcontrib><creatorcontrib>Spoldi, E</creatorcontrib><creatorcontrib>Forti, F</creatorcontrib><creatorcontrib>Sala, C</creatorcontrib><creatorcontrib>Magnoni, F</creatorcontrib><creatorcontrib>Deho, G</creatorcontrib><creatorcontrib>Ghisotti, D</creatorcontrib><title>Expression of phage P4 integrase is regulated negatively by both Int and Vis</title><title>Journal of general virology</title><addtitle>J Gen Virol</addtitle><description>Dipartimento di Scienze Biomolecolari e Biotecnologie, Università degli Studi di Milano, Via Celoria 26, 20133 Milano, Italy
Correspondence D. Ghisotti Daniela.Ghisotti{at}unimi.it
Phage P4 int gene encodes the integrase responsible for phage integration into and excision from the Escherichia coli chromosome. Here, the data showing that P4 int expression is regulated in a complex manner at different levels are presented. First of all, the P int promoter is regulated negatively by both Int and Vis, the P4 excisionase. The N-terminal portion of Int appears to be sufficient for such a negative autoregulation, suggesting that the Int N terminus is implicated in DNA binding. Second, full-length transcripts covering the entire int gene could be detected only upon P4 infection, whereas in P4 lysogens only short 5'-end covering transcripts were detectable. On the other hand, transcripts covering the 5'-end of int were also very abundant upon infection. It thus appears that premature transcription termination and/or mRNA degradation play a role in Int-negative regulation both on the basal prophage transcription and upon infection. Finally, comparison between P int lacZ transcriptional and translational fusions suggests that Vis regulates Int expression post-transcriptionally. The findings that Vis is also an RNA-binding protein and that Int may be translated from two different start codons have implications on possible regulation models of Int expression.
Present address: Max F. Perutz Laboratories at the Vienna Biocenter, Department of Microbiology and Genetics, University of Vienna, 1030 Vienna, Austria.
Present address: Keryos, Via della Filanda 5, 20060 Gessate (MI), Italy.
Present address: Molmed SpA, Via Olgettina 58, 20132 Milano, Italy.</description><subject>Artificial Gene Fusion</subject><subject>Attachment Sites, Microbiological</subject><subject>Base Sequence</subject><subject>beta-Galactosidase - analysis</subject><subject>beta-Galactosidase - genetics</subject><subject>Biological and medical sciences</subject><subject>Coliphages - enzymology</subject><subject>Coliphages - genetics</subject><subject>DNA-Binding Proteins - biosynthesis</subject><subject>DNA-Binding Proteins - genetics</subject><subject>DNA-Binding Proteins - physiology</subject><subject>Escherichia coli</subject><subject>Escherichia coli - genetics</subject><subject>Escherichia coli - virology</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Gene Expression Regulation, Viral</subject><subject>Genes, Reporter</subject><subject>Integrases - biosynthesis</subject><subject>Integrases - genetics</subject><subject>Microbiology</subject><subject>Miscellaneous</subject><subject>Molecular Sequence Data</subject><subject>Phage P4</subject><subject>Protein Binding</subject><subject>Protein Structure, Tertiary</subject><subject>RNA, Messenger - analysis</subject><subject>RNA, Viral - analysis</subject><subject>Viral Proteins - physiology</subject><subject>Virology</subject><issn>0022-1317</issn><issn>1465-2099</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2006</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqF0MFr2zAUBnAxWta023HXoUtLL87ek-RIPo7SbYFAe-h2FbL87Gg4diY5XfPfV20CPRYEQujHex8fY18Q5ghV9e0xxDnMDRpdFvCBzVAtykLknxM2AxCiQIn6jJ2n9BcAlSr1R3aGC6M0ymrGVrdP20gphXHgY8u3a9cRv1c8DBN10SXiIfFI3a53EzV8oM5N4ZH6Pa_zGac1Xw4Td0PD_4T0iZ22rk_0-XhfsN8_bh9ufhWru5_Lm--rwqsKppwOZAW6ldqDNiY_GywFYI3KC6ob0xgqKylIG3BeCJJQg1dgHJZatKW8YFeHuds4_ttRmuwmJE997wYad8kuzKJUgPguxCqvkKAzLA7QxzGlSK3dxrBxcW8R7EvPNvdswb72bCH7r8fBu3pDzZs-FpvB5RG45F3fRjf4kN6crl4zZnd9cOvQrf-HSLajYRNyjDqML0uNtsYKJaR8BvsEkd4</recordid><startdate>20060801</startdate><enddate>20060801</enddate><creator>Piazzolla, D</creator><creator>Cali, S</creator><creator>Spoldi, E</creator><creator>Forti, F</creator><creator>Sala, C</creator><creator>Magnoni, F</creator><creator>Deho, G</creator><creator>Ghisotti, D</creator><general>Soc General Microbiol</general><general>Society for General Microbiology</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>7U9</scope><scope>C1K</scope><scope>H94</scope><scope>7X8</scope></search><sort><creationdate>20060801</creationdate><title>Expression of phage P4 integrase is regulated negatively by both Int and Vis</title><author>Piazzolla, D ; Cali, S ; Spoldi, E ; Forti, F ; Sala, C ; Magnoni, F ; Deho, G ; Ghisotti, D</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c490t-2003907f37c0788200d15201b14c2ebd8d8e5932e780ac22e30b0c408a1572f53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2006</creationdate><topic>Artificial Gene Fusion</topic><topic>Attachment Sites, Microbiological</topic><topic>Base Sequence</topic><topic>beta-Galactosidase - analysis</topic><topic>beta-Galactosidase - genetics</topic><topic>Biological and medical sciences</topic><topic>Coliphages - enzymology</topic><topic>Coliphages - genetics</topic><topic>DNA-Binding Proteins - biosynthesis</topic><topic>DNA-Binding Proteins - genetics</topic><topic>DNA-Binding Proteins - physiology</topic><topic>Escherichia coli</topic><topic>Escherichia coli - genetics</topic><topic>Escherichia coli - virology</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Gene Expression Regulation, Viral</topic><topic>Genes, Reporter</topic><topic>Integrases - biosynthesis</topic><topic>Integrases - genetics</topic><topic>Microbiology</topic><topic>Miscellaneous</topic><topic>Molecular Sequence Data</topic><topic>Phage P4</topic><topic>Protein Binding</topic><topic>Protein Structure, Tertiary</topic><topic>RNA, Messenger - analysis</topic><topic>RNA, Viral - analysis</topic><topic>Viral Proteins - physiology</topic><topic>Virology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Piazzolla, D</creatorcontrib><creatorcontrib>Cali, S</creatorcontrib><creatorcontrib>Spoldi, E</creatorcontrib><creatorcontrib>Forti, F</creatorcontrib><creatorcontrib>Sala, C</creatorcontrib><creatorcontrib>Magnoni, F</creatorcontrib><creatorcontrib>Deho, G</creatorcontrib><creatorcontrib>Ghisotti, D</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>Virology and AIDS Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of general virology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Piazzolla, D</au><au>Cali, S</au><au>Spoldi, E</au><au>Forti, F</au><au>Sala, C</au><au>Magnoni, F</au><au>Deho, G</au><au>Ghisotti, D</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Expression of phage P4 integrase is regulated negatively by both Int and Vis</atitle><jtitle>Journal of general virology</jtitle><addtitle>J Gen Virol</addtitle><date>2006-08-01</date><risdate>2006</risdate><volume>87</volume><issue>8</issue><spage>2423</spage><epage>2431</epage><pages>2423-2431</pages><issn>0022-1317</issn><eissn>1465-2099</eissn><coden>JGVIAY</coden><abstract>Dipartimento di Scienze Biomolecolari e Biotecnologie, Università degli Studi di Milano, Via Celoria 26, 20133 Milano, Italy
Correspondence D. Ghisotti Daniela.Ghisotti{at}unimi.it
Phage P4 int gene encodes the integrase responsible for phage integration into and excision from the Escherichia coli chromosome. Here, the data showing that P4 int expression is regulated in a complex manner at different levels are presented. First of all, the P int promoter is regulated negatively by both Int and Vis, the P4 excisionase. The N-terminal portion of Int appears to be sufficient for such a negative autoregulation, suggesting that the Int N terminus is implicated in DNA binding. Second, full-length transcripts covering the entire int gene could be detected only upon P4 infection, whereas in P4 lysogens only short 5'-end covering transcripts were detectable. On the other hand, transcripts covering the 5'-end of int were also very abundant upon infection. It thus appears that premature transcription termination and/or mRNA degradation play a role in Int-negative regulation both on the basal prophage transcription and upon infection. Finally, comparison between P int lacZ transcriptional and translational fusions suggests that Vis regulates Int expression post-transcriptionally. The findings that Vis is also an RNA-binding protein and that Int may be translated from two different start codons have implications on possible regulation models of Int expression.
Present address: Max F. Perutz Laboratories at the Vienna Biocenter, Department of Microbiology and Genetics, University of Vienna, 1030 Vienna, Austria.
Present address: Keryos, Via della Filanda 5, 20060 Gessate (MI), Italy.
Present address: Molmed SpA, Via Olgettina 58, 20132 Milano, Italy.</abstract><cop>Reading</cop><pub>Soc General Microbiol</pub><pmid>16847139</pmid><doi>10.1099/vir.0.81875-0</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Artificial Gene Fusion Attachment Sites, Microbiological Base Sequence beta-Galactosidase - analysis beta-Galactosidase - genetics Biological and medical sciences Coliphages - enzymology Coliphages - genetics DNA-Binding Proteins - biosynthesis DNA-Binding Proteins - genetics DNA-Binding Proteins - physiology Escherichia coli Escherichia coli - genetics Escherichia coli - virology Fundamental and applied biological sciences. Psychology Gene Expression Regulation, Viral Genes, Reporter Integrases - biosynthesis Integrases - genetics Microbiology Miscellaneous Molecular Sequence Data Phage P4 Protein Binding Protein Structure, Tertiary RNA, Messenger - analysis RNA, Viral - analysis Viral Proteins - physiology Virology |
title | Expression of phage P4 integrase is regulated negatively by both Int and Vis |
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