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Polynucleotide phosphorylase: Not merely an RNase but a pivotal post-transcriptional regulator

Almost 60 years ago, Severo Ochoa was awarded the Nobel Prize in Physiology or Medicine for his discovery of the enzymatic synthesis of RNA by polynucleotide phosphorylase (PNPase). Although this discovery provided an important tool for deciphering the genetic code, subsequent work revealed that the...

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Detalles Bibliográficos
Autores principales: Cameron, Todd A., Matz, Lisa M., De Lay, Nicholas R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6181284/
https://www.ncbi.nlm.nih.gov/pubmed/30307990
http://dx.doi.org/10.1371/journal.pgen.1007654
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author Cameron, Todd A.
Matz, Lisa M.
De Lay, Nicholas R.
author_facet Cameron, Todd A.
Matz, Lisa M.
De Lay, Nicholas R.
author_sort Cameron, Todd A.
collection PubMed
description Almost 60 years ago, Severo Ochoa was awarded the Nobel Prize in Physiology or Medicine for his discovery of the enzymatic synthesis of RNA by polynucleotide phosphorylase (PNPase). Although this discovery provided an important tool for deciphering the genetic code, subsequent work revealed that the predominant function of PNPase in bacteria and eukaryotes is catalyzing the reverse reaction, i.e., the release of ribonucleotides from RNA. PNPase has a crucial role in RNA metabolism in bacteria and eukaryotes mainly through its roles in processing and degrading RNAs, but additional functions in RNA metabolism have recently been reported for this enzyme. Here, we discuss these established and noncanonical functions for PNPase and the possibility that the major impact of PNPase on cell physiology is through its unorthodox roles.
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spelling pubmed-61812842018-10-26 Polynucleotide phosphorylase: Not merely an RNase but a pivotal post-transcriptional regulator Cameron, Todd A. Matz, Lisa M. De Lay, Nicholas R. PLoS Genet Review Almost 60 years ago, Severo Ochoa was awarded the Nobel Prize in Physiology or Medicine for his discovery of the enzymatic synthesis of RNA by polynucleotide phosphorylase (PNPase). Although this discovery provided an important tool for deciphering the genetic code, subsequent work revealed that the predominant function of PNPase in bacteria and eukaryotes is catalyzing the reverse reaction, i.e., the release of ribonucleotides from RNA. PNPase has a crucial role in RNA metabolism in bacteria and eukaryotes mainly through its roles in processing and degrading RNAs, but additional functions in RNA metabolism have recently been reported for this enzyme. Here, we discuss these established and noncanonical functions for PNPase and the possibility that the major impact of PNPase on cell physiology is through its unorthodox roles. Public Library of Science 2018-10-11 /pmc/articles/PMC6181284/ /pubmed/30307990 http://dx.doi.org/10.1371/journal.pgen.1007654 Text en © 2018 Cameron et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Review
Cameron, Todd A.
Matz, Lisa M.
De Lay, Nicholas R.
Polynucleotide phosphorylase: Not merely an RNase but a pivotal post-transcriptional regulator
title Polynucleotide phosphorylase: Not merely an RNase but a pivotal post-transcriptional regulator
title_full Polynucleotide phosphorylase: Not merely an RNase but a pivotal post-transcriptional regulator
title_fullStr Polynucleotide phosphorylase: Not merely an RNase but a pivotal post-transcriptional regulator
title_full_unstemmed Polynucleotide phosphorylase: Not merely an RNase but a pivotal post-transcriptional regulator
title_short Polynucleotide phosphorylase: Not merely an RNase but a pivotal post-transcriptional regulator
title_sort polynucleotide phosphorylase: not merely an rnase but a pivotal post-transcriptional regulator
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6181284/
https://www.ncbi.nlm.nih.gov/pubmed/30307990
http://dx.doi.org/10.1371/journal.pgen.1007654
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