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Interplay between the catabolite repression control protein Crc, Hfq and RNA in Hfq-dependent translational regulation in Pseudomonas aeruginosa.
Sonnleitner, Elisabeth; Wulf, Alexander; Campagne, Sébastien; Pei, Xue-Yuan; Wolfinger, Michael T; Forlani, Giada; Prindl, Konstantin; Abdou, Laetitia; Resch, Armin; Allain, Frederic H-T; Luisi, Ben F; Urlaub, Henning; Bläsi, Udo.
Afiliação
  • Sonnleitner E; Department of Microbiology, Immunobiology and Genetics, Max F. Perutz Laboratories, University of Vienna, Vienna Biocenter, Dr. Bohrgasse 9, 1030 Vienna, Austria.
  • Wulf A; Biophysical Mass Spectrometry Group, Max Planck Institute for Biophysical Chemistry, 37077 Göttingen, Germany.
  • Campagne S; Institute of Molecular Biology and Biophysics, ETH Zürich, 8093 Zürich, Switzerland.
  • Pei XY; Department of Biochemistry, University of Cambridge, Cambridge CB2 1GA, UK.
  • Wolfinger MT; Institute of Theoretical Chemistry, University of Vienna, 1090 Vienna, Austria.
  • Forlani G; Center for Anatomy and Cell Biology, Medical University of Vienna, 1090 Vienna, Austria.
  • Prindl K; Department of Microbiology, Immunobiology and Genetics, Max F. Perutz Laboratories, University of Vienna, Vienna Biocenter, Dr. Bohrgasse 9, 1030 Vienna, Austria.
  • Abdou L; Department of Microbiology, Immunobiology and Genetics, Max F. Perutz Laboratories, University of Vienna, Vienna Biocenter, Dr. Bohrgasse 9, 1030 Vienna, Austria.
  • Resch A; Department of Fundamental Microbiology, University of Lausanne, 1015 Lausanne, Switzerland.
  • Allain FH; Department of Microbiology, Immunobiology and Genetics, Max F. Perutz Laboratories, University of Vienna, Vienna Biocenter, Dr. Bohrgasse 9, 1030 Vienna, Austria.
  • Luisi BF; Institute of Molecular Biology and Biophysics, ETH Zürich, 8093 Zürich, Switzerland.
  • Urlaub H; Department of Biochemistry, University of Cambridge, Cambridge CB2 1GA, UK.
  • Bläsi U; Biophysical Mass Spectrometry Group, Max Planck Institute for Biophysical Chemistry, 37077 Göttingen, Germany.
Nucleic Acids Res ; 46(3): 1470-1485, 2018 02 16.
Article em En | MEDLINE | ID: mdl-29244160
In Pseudomonas aeruginosa the RNA chaperone Hfq and the catabolite repression control protein (Crc) act as post-transcriptional regulators during carbon catabolite repression (CCR). In this regard Crc is required for full-fledged Hfq-mediated translational repression of catabolic genes. RNAseq based transcriptome analyses revealed a significant overlap between the Crc and Hfq regulons, which in conjunction with genetic data supported a concerted action of both proteins. Biochemical and biophysical approaches further suggest that Crc and Hfq form an assembly in the presence of RNAs containing A-rich motifs, and that Crc interacts with both, Hfq and RNA. Through these interactions, Crc enhances the stability of Hfq/Crc/RNA complexes, which can explain its facilitating role in Hfq-mediated translational repression. Hence, these studies revealed for the first time insights into how an interacting protein can modulate Hfq function. Moreover, Crc is shown to interfere with binding of a regulatory RNA to Hfq, which bears implications for riboregulation. These results are discussed in terms of a working model, wherein Crc prioritizes the function of Hfq toward utilization of favored carbon sources.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Pseudomonas aeruginosa / Proteínas Repressoras / Proteínas de Bactérias / Biossíntese de Proteínas / RNA Bacteriano / Fator Proteico 1 do Hospedeiro / Repressão Catabólica Tipo de estudo: Prognostic_studies Idioma: En Revista: Nucleic Acids Res Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Áustria

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Pseudomonas aeruginosa / Proteínas Repressoras / Proteínas de Bactérias / Biossíntese de Proteínas / RNA Bacteriano / Fator Proteico 1 do Hospedeiro / Repressão Catabólica Tipo de estudo: Prognostic_studies Idioma: En Revista: Nucleic Acids Res Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Áustria