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  A conserved RpoS-dependent small RNA controls the synthesis of major porin OmpD

Fröhlich, K. S., Papenfort, K., Berger, A. A., & Vogel, J. (2012). A conserved RpoS-dependent small RNA controls the synthesis of major porin OmpD. NUCLEIC ACIDS RESEARCH, 40(8), 3623-3640. doi:10.1093/nar/gkr1156.

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Genre: Zeitschriftenartikel
Alternativer Titel : Nucleic Acids Res.

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Nucleic_Acids_Res_2012_40_3623.pdf (Verlagsversion), 5MB
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This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
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Fröhlich, Kathrin S.1, Autor           
Papenfort, Kai1, Autor           
Berger, Allison A.1, Autor           
Vogel, Jörg1, Autor           
Affiliations:
1Max-Planck Research Group RNA Biology, Max Planck Institute for Infection Biology, Max Planck Society, ou_1664150              

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 Zusammenfassung: A remarkable feature of many small non-coding RNAs (sRNAs) of Escherichia coli and Salmonella is their accumulation in the stationary phase of bacterial growth. Several stress response regulators and sigma factors have been reported to direct the transcription of stationary phase-specific sRNAs, but a widely conserved sRNA gene that is controlled by the major stationary phase and stress sigma factor, Sigma(S) (RpoS), has remained elusive. We have studied in Salmonella the conserved SdsR sRNA, previously known as RyeB, one of the most abundant stationary phase-specific sRNAs in E. coli. Alignments of the sdsR promoter region and genetic analysis strongly suggest that this sRNA gene is selectively transcribed by Sigma(S). We show that SdsR down-regulates the synthesis of the major Salmonella porin OmpD by Hfq-dependent base pairing; SdsR thus represents the fourth sRNA to regulate this major outer membrane porin. Similar to the InvR, MicC and RybB sRNAs, SdsR recognizes the ompD mRNA in the coding sequence, suggesting that this mRNA may be primarily targeted downstream of the start codon. The SdsR-binding site in ompD was localized by 3'-RACE, an experimental approach that promises to be of use in predicting other sRNA-target interactions in bacteria.

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Sprache(n): eng - English
 Datum: 2012-04
 Publikationsstatus: Erschienen
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 Art der Begutachtung: Expertenbegutachtung
 Identifikatoren: eDoc: 610069
ISI: 000303333500034
DOI: 10.1093/nar/gkr1156
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Titel: NUCLEIC ACIDS RESEARCH
  Alternativer Titel : Nucleic Acids Res.
Genre der Quelle: Zeitschrift
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Ort, Verlag, Ausgabe: OXFORD : OXFORD UNIV PRESS
Seiten: - Band / Heft: 40 (8) Artikelnummer: - Start- / Endseite: 3623 - 3640 Identifikator: ISSN: 0305-1048