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Transcription and replication mechanisms of Bunyaviridae and Arenaviridae L proteins
Bunyaviridae and Arenaviridae virus families include an important number of highly pathogenic viruses for humans. They are enveloped viruses with negative stranded RNA genomes divided into three (bunyaviruses) or two (arenaviruses) segments. Each genome segment is coated by the viral nucleoproteins...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier B.V.
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7114536/ https://www.ncbi.nlm.nih.gov/pubmed/28137457 http://dx.doi.org/10.1016/j.virusres.2017.01.018 |
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author | Ferron, François Weber, Friedemann de la Torre, Juan Carlos Reguera, Juan |
author_facet | Ferron, François Weber, Friedemann de la Torre, Juan Carlos Reguera, Juan |
author_sort | Ferron, François |
collection | PubMed |
description | Bunyaviridae and Arenaviridae virus families include an important number of highly pathogenic viruses for humans. They are enveloped viruses with negative stranded RNA genomes divided into three (bunyaviruses) or two (arenaviruses) segments. Each genome segment is coated by the viral nucleoproteins (NPs) and the polymerase (L protein) to form a functional ribonucleoprotein (RNP) complex. The viral RNP provides the necessary context on which the L protein carries out the biosynthetic processes of RNA replication and gene transcription. Decades of research have provided a good understanding of the molecular processes underlying RNA synthesis, both RNA replication and gene transcription, for these two families of viruses. In this review we will provide a global view of the common features, as well as differences, of the molecular biology of Bunyaviridae and Arenaviridae. We will also describe structures of protein and protein-RNA complexes so far determined for these viral families, mainly focusing on the L protein, and discuss their implications for understanding the mechanisms of viral RNA replication and gene transcription within the architecture of viral RNPs, also taking into account the cellular context in which these processes occur. Finally, we will discuss the implications of these structural findings for the development of antiviral drugs to treat human diseases caused by members of the Bunyaviridae and Arenaviridae families. |
format | Online Article Text |
id | pubmed-7114536 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Elsevier B.V. |
record_format | MEDLINE/PubMed |
spelling | pubmed-71145362020-04-02 Transcription and replication mechanisms of Bunyaviridae and Arenaviridae L proteins Ferron, François Weber, Friedemann de la Torre, Juan Carlos Reguera, Juan Virus Res Article Bunyaviridae and Arenaviridae virus families include an important number of highly pathogenic viruses for humans. They are enveloped viruses with negative stranded RNA genomes divided into three (bunyaviruses) or two (arenaviruses) segments. Each genome segment is coated by the viral nucleoproteins (NPs) and the polymerase (L protein) to form a functional ribonucleoprotein (RNP) complex. The viral RNP provides the necessary context on which the L protein carries out the biosynthetic processes of RNA replication and gene transcription. Decades of research have provided a good understanding of the molecular processes underlying RNA synthesis, both RNA replication and gene transcription, for these two families of viruses. In this review we will provide a global view of the common features, as well as differences, of the molecular biology of Bunyaviridae and Arenaviridae. We will also describe structures of protein and protein-RNA complexes so far determined for these viral families, mainly focusing on the L protein, and discuss their implications for understanding the mechanisms of viral RNA replication and gene transcription within the architecture of viral RNPs, also taking into account the cellular context in which these processes occur. Finally, we will discuss the implications of these structural findings for the development of antiviral drugs to treat human diseases caused by members of the Bunyaviridae and Arenaviridae families. Elsevier B.V. 2017-04-15 2017-01-27 /pmc/articles/PMC7114536/ /pubmed/28137457 http://dx.doi.org/10.1016/j.virusres.2017.01.018 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 | Article Ferron, François Weber, Friedemann de la Torre, Juan Carlos Reguera, Juan Transcription and replication mechanisms of Bunyaviridae and Arenaviridae L proteins |
title | Transcription and replication mechanisms of Bunyaviridae and Arenaviridae L proteins |
title_full | Transcription and replication mechanisms of Bunyaviridae and Arenaviridae L proteins |
title_fullStr | Transcription and replication mechanisms of Bunyaviridae and Arenaviridae L proteins |
title_full_unstemmed | Transcription and replication mechanisms of Bunyaviridae and Arenaviridae L proteins |
title_short | Transcription and replication mechanisms of Bunyaviridae and Arenaviridae L proteins |
title_sort | transcription and replication mechanisms of bunyaviridae and arenaviridae l proteins |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7114536/ https://www.ncbi.nlm.nih.gov/pubmed/28137457 http://dx.doi.org/10.1016/j.virusres.2017.01.018 |
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