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Cystoviral RNA-directed RNA polymerases: Regulation of RNA synthesis on multiple time and length scales
P2, an RNA-directed RNA polymerase (RdRP), is encoded on the largest of the three segments of the double-stranded RNA genome of cystoviruses. P2 performs the dual tasks of replication and transcription de novo on single-stranded RNA templates, and plays a critical role in the viral life-cycle. Work...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Elsevier B.V.
2017
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5476504/ https://www.ncbi.nlm.nih.gov/pubmed/28104452 http://dx.doi.org/10.1016/j.virusres.2017.01.006 |
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author | Alphonse, Sébastien Ghose, Ranajeet |
author_facet | Alphonse, Sébastien Ghose, Ranajeet |
author_sort | Alphonse, Sébastien |
collection | PubMed |
description | P2, an RNA-directed RNA polymerase (RdRP), is encoded on the largest of the three segments of the double-stranded RNA genome of cystoviruses. P2 performs the dual tasks of replication and transcription de novo on single-stranded RNA templates, and plays a critical role in the viral life-cycle. Work over the last few decades has yielded a wealth of biochemical and structural information on the functional regulation of P2, on its role in the spatiotemporal regulation of RNA synthesis and its variability across the Cystoviridae family. These range from atomic resolution snapshots of P2 trapped in functionally significant states, in complex with catalytic/structural metal ions, polynucleotide templates and substrate nucleoside triphosphates, to P2 in the context of viral capsids providing structural insight into the assembly of supramolecular complexes and regulatory interactions therein. They include in vitro biochemical studies using P2 purified to homogeneity and in vivo studies utilizing infectious core particles. Recent advances in experimental techniques have also allowed access to the temporal dimension and enabled the characterization of dynamics of P2 on the sub-nanosecond to millisecond timescale through measurements of nuclear spin relaxation in solution and single molecule studies of transcription from seconds to minutes. Below we summarize the most significant results that provide critical insight into the role of P2 in regulating RNA synthesis in cystoviruses. |
format | Online Article Text |
id | pubmed-5476504 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Elsevier B.V. |
record_format | MEDLINE/PubMed |
spelling | pubmed-54765042018-04-15 Cystoviral RNA-directed RNA polymerases: Regulation of RNA synthesis on multiple time and length scales Alphonse, Sébastien Ghose, Ranajeet Virus Res Review P2, an RNA-directed RNA polymerase (RdRP), is encoded on the largest of the three segments of the double-stranded RNA genome of cystoviruses. P2 performs the dual tasks of replication and transcription de novo on single-stranded RNA templates, and plays a critical role in the viral life-cycle. Work over the last few decades has yielded a wealth of biochemical and structural information on the functional regulation of P2, on its role in the spatiotemporal regulation of RNA synthesis and its variability across the Cystoviridae family. These range from atomic resolution snapshots of P2 trapped in functionally significant states, in complex with catalytic/structural metal ions, polynucleotide templates and substrate nucleoside triphosphates, to P2 in the context of viral capsids providing structural insight into the assembly of supramolecular complexes and regulatory interactions therein. They include in vitro biochemical studies using P2 purified to homogeneity and in vivo studies utilizing infectious core particles. Recent advances in experimental techniques have also allowed access to the temporal dimension and enabled the characterization of dynamics of P2 on the sub-nanosecond to millisecond timescale through measurements of nuclear spin relaxation in solution and single molecule studies of transcription from seconds to minutes. Below we summarize the most significant results that provide critical insight into the role of P2 in regulating RNA synthesis in cystoviruses. Elsevier B.V. 2017-04-15 2017-01-16 /pmc/articles/PMC5476504/ /pubmed/28104452 http://dx.doi.org/10.1016/j.virusres.2017.01.006 Text en © 2017 Elsevier B.V. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active. |
spellingShingle | Review Alphonse, Sébastien Ghose, Ranajeet Cystoviral RNA-directed RNA polymerases: Regulation of RNA synthesis on multiple time and length scales |
title | Cystoviral RNA-directed RNA polymerases: Regulation of RNA synthesis on multiple time and length scales |
title_full | Cystoviral RNA-directed RNA polymerases: Regulation of RNA synthesis on multiple time and length scales |
title_fullStr | Cystoviral RNA-directed RNA polymerases: Regulation of RNA synthesis on multiple time and length scales |
title_full_unstemmed | Cystoviral RNA-directed RNA polymerases: Regulation of RNA synthesis on multiple time and length scales |
title_short | Cystoviral RNA-directed RNA polymerases: Regulation of RNA synthesis on multiple time and length scales |
title_sort | cystoviral rna-directed rna polymerases: regulation of rna synthesis on multiple time and length scales |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5476504/ https://www.ncbi.nlm.nih.gov/pubmed/28104452 http://dx.doi.org/10.1016/j.virusres.2017.01.006 |
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