Literature DB >> 19215773

The role of 3'-5' exoribonucleases in RNA degradation.

José M Andrade1, Vânia Pobre, Inês J Silva, Susana Domingues, Cecília M Arraiano.   

Abstract

RNA degradation is a major process controlling RNA levels and plays a central role in cell metabolism. From the labile messenger RNA to the more stable noncoding RNAs (mostly rRNA and tRNA, but also the expanding class of small regulatory RNAs) all molecules are eventually degraded. Elimination of superfluous transcripts includes RNAs whose expression is no longer required, but also the removal of defective RNAs. Consequently, RNA degradation is an inherent step in RNA quality control mechanisms. Furthermore, it contributes to the recycling of the nucleotide pool in the cell. Escherichia coli has eight 3'-5' exoribonucleases, which are involved in multiple RNA metabolic pathways. However, only four exoribonucleases appear to accomplish all RNA degradative activities: polynucleotide phosphorylase (PNPase), ribonuclease II (RNase II), RNase R, and oligoribonuclease. Here, we summarize the available information on the role of bacterial 3'-5' exoribonucleases in the degradation of different substrates, highlighting the most recent data that have contributed to the understanding of the diverse modes of operation of these degradative enzymes.

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Year:  2009        PMID: 19215773     DOI: 10.1016/S0079-6603(08)00805-2

Source DB:  PubMed          Journal:  Prog Mol Biol Transl Sci        ISSN: 1877-1173            Impact factor:   3.622


  53 in total

1.  Novel role for RNase PH in the degradation of structured RNA.

Authors:  Chaitanya Jain
Journal:  J Bacteriol       Date:  2012-05-18       Impact factor: 3.490

2.  Comparison of EMSA and SPR for the characterization of RNA-RNase II complexes.

Authors:  Rute G Matos; Ana Barbas; Cecília M Arraiano
Journal:  Protein J       Date:  2010-08       Impact factor: 2.371

3.  CsrA Participates in a PNPase Autoregulatory Mechanism by Selectively Repressing Translation of pnp Transcripts That Have Been Previously Processed by RNase III and PNPase.

Authors:  Hongmarn Park; Helen Yakhnin; Michael Connolly; Tony Romeo; Paul Babitzke
Journal:  J Bacteriol       Date:  2015-10-05       Impact factor: 3.490

4.  Direct observation of processive exoribonuclease motion using optical tweezers.

Authors:  Furqan M Fazal; Daniel J Koslover; Ben F Luisi; Steven M Block
Journal:  Proc Natl Acad Sci U S A       Date:  2015-11-23       Impact factor: 11.205

5.  RNase I Modulates Escherichia coli Motility, Metabolism, and Resistance.

Authors:  Yashasvika Duggal; Benjamin M Fontaine; Deanna M Dailey; Gang Ning; Emily E Weinert
Journal:  ACS Chem Biol       Date:  2020-07-02       Impact factor: 5.100

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.  Ribosomes regulate the stability and action of the exoribonuclease RNase R.

Authors:  Wenxing Liang; Murray P Deutscher
Journal:  J Biol Chem       Date:  2013-10-16       Impact factor: 5.157

8.  How a CCA sequence protects mature tRNAs and tRNA precursors from action of the processing enzyme RNase BN/RNase Z.

Authors:  Tanmay Dutta; Arun Malhotra; Murray P Deutscher
Journal:  J Biol Chem       Date:  2013-09-10       Impact factor: 5.157

9.  Short RNA half-lives in the slow-growing marine cyanobacterium Prochlorococcus.

Authors:  Claudia Steglich; Debbie Lindell; Matthias Futschik; Trent Rector; Robert Steen; Sallie W Chisholm
Journal:  Genome Biol       Date:  2010-05-19       Impact factor: 13.583

10.  The N-terminus of GalE induces tmRNA activity in Escherichia coli.

Authors:  Zachary C Ruhe; Christopher S Hayes
Journal:  PLoS One       Date:  2010-12-07       Impact factor: 3.240

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