A novel Hfq‐dependent sRNA that is under FNR control and is synthesized in oxygen limitation in Neisseria meningitidis

Summary Small non‐coding RNAs (sRNA) are emerging as key elements of post‐transcriptional gene regulation in bacteria. The conserved Hfq protein is thought to function as an RNA chaperone and facilitate base‐pairing between sRNAs and mRNA targets. In this study we identify a novel sRNA of Neisseria...

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Veröffentlicht in:Molecular microbiology 2011-04, Vol.80 (2), p.507-523
Hauptverfasser: Fantappiè, Laura, Oriente, Francesca, Muzzi, Alessandro, Serruto, Davide, Scarlato, Vincenzo, Delany, Isabel
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container_issue 2
container_start_page 507
container_title Molecular microbiology
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creator Fantappiè, Laura
Oriente, Francesca
Muzzi, Alessandro
Serruto, Davide
Scarlato, Vincenzo
Delany, Isabel
description Summary Small non‐coding RNAs (sRNA) are emerging as key elements of post‐transcriptional gene regulation in bacteria. The conserved Hfq protein is thought to function as an RNA chaperone and facilitate base‐pairing between sRNAs and mRNA targets. In this study we identify a novel sRNA of Neisseria meningitidis through global gene expression studies of regulated transcripts in the Hfq mutant. The synthesis of this sRNA, named AniS, is anaerobically induced through activation of its promoter by the FNR global regulator. Whole‐genome expression analyses led to the identification of putative mRNA targets, two of which are predicted to base pair with AniS. We show that Hfq binds the AniS transcript in vitro and is necessary for the downregulation of the identified target mRNAs in vivo. Contrary to many Hfq‐dependent sRNA of the Enterobacteriaceae, Hfq promotes decay of AniS in N. meningitidis. Our analysis shows that the AniS regulator is part of the FNR regulon and may be responsible for the downregulation of FNR‐repressed genes. Furthermore the presence of similar conserved regulatory sequences in all Neisseria spp. to date suggests that an analogous FNR‐regulated sRNA, with a variable 5′ sequence, may be ubiquitous to all commensals and pathogens of the Genus.
doi_str_mv 10.1111/j.1365-2958.2011.07592.x
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The conserved Hfq protein is thought to function as an RNA chaperone and facilitate base‐pairing between sRNAs and mRNA targets. In this study we identify a novel sRNA of Neisseria meningitidis through global gene expression studies of regulated transcripts in the Hfq mutant. The synthesis of this sRNA, named AniS, is anaerobically induced through activation of its promoter by the FNR global regulator. Whole‐genome expression analyses led to the identification of putative mRNA targets, two of which are predicted to base pair with AniS. We show that Hfq binds the AniS transcript in vitro and is necessary for the downregulation of the identified target mRNAs in vivo. Contrary to many Hfq‐dependent sRNA of the Enterobacteriaceae, Hfq promotes decay of AniS in N. meningitidis. Our analysis shows that the AniS regulator is part of the FNR regulon and may be responsible for the downregulation of FNR‐repressed genes. 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Psychology</topic><topic>Gene expression</topic><topic>Gene Expression Profiling</topic><topic>Gene Expression Regulation, Bacterial</topic><topic>Genomes</topic><topic>Host Factor 1 Protein - metabolism</topic><topic>Microbiology</topic><topic>Miscellaneous</topic><topic>Mutation</topic><topic>Neisseria meningitidis - genetics</topic><topic>Neisseria meningitidis - metabolism</topic><topic>Oxygen</topic><topic>Oxygen - metabolism</topic><topic>Protein Binding</topic><topic>Ribonucleic acid</topic><topic>RNA</topic><topic>RNA Stability</topic><topic>RNA, Messenger - metabolism</topic><topic>RNA, Small Interfering - biosynthesis</topic><topic>Studies</topic><topic>Transcription Factors - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Fantappiè, Laura</creatorcontrib><creatorcontrib>Oriente, Francesca</creatorcontrib><creatorcontrib>Muzzi, Alessandro</creatorcontrib><creatorcontrib>Serruto, Davide</creatorcontrib><creatorcontrib>Scarlato, Vincenzo</creatorcontrib><creatorcontrib>Delany, Isabel</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>Calcium &amp; 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><collection>MEDLINE - Academic</collection><jtitle>Molecular microbiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Fantappiè, Laura</au><au>Oriente, Francesca</au><au>Muzzi, Alessandro</au><au>Serruto, Davide</au><au>Scarlato, Vincenzo</au><au>Delany, Isabel</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A novel Hfq‐dependent sRNA that is under FNR control and is synthesized in oxygen limitation in Neisseria meningitidis</atitle><jtitle>Molecular microbiology</jtitle><addtitle>Mol Microbiol</addtitle><date>2011-04</date><risdate>2011</risdate><volume>80</volume><issue>2</issue><spage>507</spage><epage>523</epage><pages>507-523</pages><issn>0950-382X</issn><eissn>1365-2958</eissn><abstract>Summary Small non‐coding RNAs (sRNA) are emerging as key elements of post‐transcriptional gene regulation in bacteria. The conserved Hfq protein is thought to function as an RNA chaperone and facilitate base‐pairing between sRNAs and mRNA targets. In this study we identify a novel sRNA of Neisseria meningitidis through global gene expression studies of regulated transcripts in the Hfq mutant. The synthesis of this sRNA, named AniS, is anaerobically induced through activation of its promoter by the FNR global regulator. Whole‐genome expression analyses led to the identification of putative mRNA targets, two of which are predicted to base pair with AniS. We show that Hfq binds the AniS transcript in vitro and is necessary for the downregulation of the identified target mRNAs in vivo. Contrary to many Hfq‐dependent sRNA of the Enterobacteriaceae, Hfq promotes decay of AniS in N. meningitidis. Our analysis shows that the AniS regulator is part of the FNR regulon and may be responsible for the downregulation of FNR‐repressed genes. 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source MEDLINE; Wiley Free Content; EZB-FREE-00999 freely available EZB journals; Wiley Online Library All Journals
subjects Bacteria
Bacteriology
Biological and medical sciences
Fundamental and applied biological sciences. Psychology
Gene expression
Gene Expression Profiling
Gene Expression Regulation, Bacterial
Genomes
Host Factor 1 Protein - metabolism
Microbiology
Miscellaneous
Mutation
Neisseria meningitidis - genetics
Neisseria meningitidis - metabolism
Oxygen
Oxygen - metabolism
Protein Binding
Ribonucleic acid
RNA
RNA Stability
RNA, Messenger - metabolism
RNA, Small Interfering - biosynthesis
Studies
Transcription Factors - metabolism
title A novel Hfq‐dependent sRNA that is under FNR control and is synthesized in oxygen limitation in Neisseria meningitidis
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