Literature DB >> 23474120

RNA quality control in the nucleus: the Angels' share of RNA.

Odil Porrua1, Domenico Libri.   

Abstract

Biological processes are not exempt from errors and RNA production is not an exception to this rule. Errors can arise stochastically or be genetically fixed and systematically appear in the biochemical or cellular phenotype. In any case, quality control mechanisms are essential to minimize the potentially toxic effects of faulty RNA production or processing. Although many RNA molecules express their functional potential in the cytoplasm, as messengers, adaptors or operators of gene expression pathways, a large share of quality control occurs in the nucleus. This is likely because the early timing of occurrence and the subcellular partition make the control more efficient, at least as long as the defects can be detected ahead of the cytoplasmic phase of the RNA life cycle. One crucial point in discussing RNA quality control resides in its definition. A stringent take would imply the existence of specific mechanisms to recognize the error and the consequent repair or elimination of the faulty molecule. One example in the RNA field could be the recognition of a premature stop codon by the nonsense-mediated decay pathway, discussed elsewhere in this issue. A more relaxed view posits that the thermodynamic or kinetic aftermath of a mistake (e.g. a blockage or a delay in processing) by itself constitutes the recognition event, which triggers downstream quality control. Because whether inappropriate molecules are specifically recognized remains unclear in many cases, we will adopt the more relaxed definition of RNA quality control. RNA repair remains episodic and the degradative elimination of crippled molecules appears to be the rule. Therefore we will briefly describe the actors of RNA degradation in the nucleus. Detailed analyses of the mechanism of action of these enzymes can be found in several excellent and recent reviews, including in this issue. Finally, we will restrict our analysis to the yeast model, which is used in the majority of RNA quality control studies, but examples exist in the literature indicating that many of the principles of RNA quality control described in yeast also apply to other eukaryotes. This article is part of a Special Issue entitled: RNA Decay mechanisms.
Copyright © 2013. Published by Elsevier B.V.

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Year:  2013        PMID: 23474120     DOI: 10.1016/j.bbagrm.2013.02.012

Source DB:  PubMed          Journal:  Biochim Biophys Acta        ISSN: 0006-3002


  28 in total

1.  RNA degradation paths in a 12-subunit nuclear exosome complex.

Authors:  Debora Lika Makino; Benjamin Schuch; Elisabeth Stegmann; Marc Baumgärtner; Claire Basquin; Elena Conti
Journal:  Nature       Date:  2015-07-29       Impact factor: 49.962

2.  Telling right from wrong in life - cellular quality control.

Authors:  Georg Stoecklin; Bernd Bukau
Journal:  Nat Rev Mol Cell Biol       Date:  2013-10       Impact factor: 94.444

Review 3.  mRNA stability in the nucleus.

Authors:  Han Liu; Min Luo; Ji-kai Wen
Journal:  J Zhejiang Univ Sci B       Date:  2014-05       Impact factor: 3.066

Review 4.  Signaling to and from the RNA Polymerase III Transcription and Processing Machinery.

Authors:  Ian M Willis; Robyn D Moir
Journal:  Annu Rev Biochem       Date:  2018-01-12       Impact factor: 23.643

Review 5.  The eukaryotic RNA exosome.

Authors:  Kurt Januszyk; Christopher D Lima
Journal:  Curr Opin Struct Biol       Date:  2014-02-11       Impact factor: 6.809

6.  Target Discrimination in Nonsense-Mediated mRNA Decay Requires Upf1 ATPase Activity.

Authors:  Suzanne R Lee; Gabriel A Pratt; Fernando J Martinez; Gene W Yeo; Jens Lykke-Andersen
Journal:  Mol Cell       Date:  2015-08-06       Impact factor: 17.970

7.  The RNA Exosome Channeling and Direct Access Conformations Have Distinct In Vivo Functions.

Authors:  Jaeil Han; Ambro van Hoof
Journal:  Cell Rep       Date:  2016-09-20       Impact factor: 9.423

8.  Co-transcriptional degradation by the 5'-3' exonuclease Rat1p mediates quality control of HXK1 mRNP biogenesis in S. cerevisiae.

Authors:  Christine Mosrin-Huaman; Nadège Hervouet-Coste; A Rachid Rahmouni
Journal:  RNA Biol       Date:  2016-04-28       Impact factor: 4.652

Review 9.  The Ess1 prolyl isomerase: traffic cop of the RNA polymerase II transcription cycle.

Authors:  Steven D Hanes
Journal:  Biochim Biophys Acta       Date:  2014-02-12

Review 10.  Noncoding RNA Surveillance: The Ends Justify the Means.

Authors:  Cedric Belair; Soyeong Sim; Sandra L Wolin
Journal:  Chem Rev       Date:  2017-10-12       Impact factor: 60.622

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