Literature DB >> 16556233

RNase R affects gene expression in stationary phase: regulation of ompA.

José Marques Andrade1, Fátima Cairrão, Cecília Maria Arraiano.   

Abstract

In nature, bacteria remain mostly in the stationary phase of the life cycle. Although mRNA is a major determinant of gene expression, little is known about mRNA decay in the stationary phase. The results presented herein demonstrate that RNase R is induced in stationary phase and is involved in the post-transcriptional regulation of ompA mRNA. This work is the first report of RNase R activity on a full length mRNA. In the absence of RNase R in a single rnr mutant, higher levels of ompA mRNA are found as a consequence of the stabilization of ompA full transcript. This effect is growth-phase-specific and not a growth-rate-dependent event. These higher levels of ompA mRNA were correlated with increases in the amounts of OmpA protein. We have also analysed the role of other factors that could affect ompA mRNA stability in stationary phase. RNase E was found to have the most important role, followed by polyadenylation. PNPase also affected the decay of the ompA transcript but RNase II did not seem to contribute much to this degradation process. The participation of RNase R in poly(A)-dependent pathways of decay in stationary phase of growth is discussed. The results show that RNase R can be a modulator of gene expression in stationary phase cells.

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Year:  2006        PMID: 16556233     DOI: 10.1111/j.1365-2958.2006.05092.x

Source DB:  PubMed          Journal:  Mol Microbiol        ISSN: 0950-382X            Impact factor:   3.501


  35 in total

1.  Post-translational modification of RNase R is regulated by stress-dependent reduction in the acetylating enzyme Pka (YfiQ).

Authors:  Wenxing Liang; Murray P Deutscher
Journal:  RNA       Date:  2011-11-28       Impact factor: 4.942

2.  A novel mechanism for ribonuclease regulation: transfer-messenger RNA (tmRNA) and its associated protein SmpB regulate the stability of RNase R.

Authors:  Wenxing Liang; Murray P Deutscher
Journal:  J Biol Chem       Date:  2010-08-05       Impact factor: 5.157

3.  The response regulator SprE (RssB) is required for maintaining poly(A) polymerase I-degradosome association during stationary phase.

Authors:  Valerie J Carabetta; Thomas J Silhavy; Ileana M Cristea
Journal:  J Bacteriol       Date:  2010-05-14       Impact factor: 3.490

4.  The role of the S1 domain in exoribonucleolytic activity: substrate specificity and multimerization.

Authors:  Mónica Amblar; Ana Barbas; Paulino Gomez-Puertas; Cecília M Arraiano
Journal:  RNA       Date:  2007-01-22       Impact factor: 4.942

5.  PNPase is a key player in the regulation of small RNAs that control the expression of outer membrane proteins.

Authors:  José M Andrade; Cecília M Arraiano
Journal:  RNA       Date:  2008-01-18       Impact factor: 4.942

6.  Determination of key residues for catalysis and RNA cleavage specificity: one mutation turns RNase II into a "SUPER-ENZYME".

Authors:  Ana Barbas; Rute G Matos; Mónica Amblar; Eduardo López-Viñas; Paulino Gomez-Puertas; Cecília M Arraiano
Journal:  J Biol Chem       Date:  2009-05-19       Impact factor: 5.157

7.  The poly(A)-dependent degradation pathway of rpsO mRNA is primarily mediated by RNase R.

Authors:  José M Andrade; Eliane Hajnsdorf; Philippe Régnier; Cecília M Arraiano
Journal:  RNA       Date:  2008-12-22       Impact factor: 4.942

8.  Genomic analysis of the role of RNase R in the turnover of Pseudomonas putida mRNAs.

Authors:  Pilar Fonseca; Renata Moreno; Fernando Rojo
Journal:  J Bacteriol       Date:  2008-07-18       Impact factor: 3.490

9.  Isolation of improved free fatty acid overproducing strains of Escherichia coli via Nile red based high-throughput screening.

Authors:  Spencer W Hoover; J Tyler Youngquist; Phil A Angart; Sydnor T Withers; Rebecca M Lennen; Brian F Pfleger
Journal:  Environ Prog Sustain Energy       Date:  2011-11-17       Impact factor: 2.431

10.  Exoribonuclease R in Mycoplasma genitalium can carry out both RNA processing and degradative functions and is sensitive to RNA ribose methylation.

Authors:  Maureen S Lalonde; Yuhong Zuo; Jianwei Zhang; Xin Gong; Shaohui Wu; Arun Malhotra; Zhongwei Li
Journal:  RNA       Date:  2007-09-13       Impact factor: 4.942

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