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Molecular Studies of Genetic RNA–RNA Recombination in Brome Mosaic Virus
It is well known that DNA-based organisms rearrange and repair their genomic DNA through recombination processes, and that these rearrangements serve as a powerful source of variability and adaptation for these organisms. In RNA viruses' genetic recombination is defined as any process leading t...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Academic Press Inc. Published by Elsevier Inc.
1994
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7131656/ https://www.ncbi.nlm.nih.gov/pubmed/8191956 http://dx.doi.org/10.1016/S0065-3527(08)60051-2 |
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author | Bujarski, Jozef J. Nagy, Peter D. Flasinski, Stanislaw |
author_facet | Bujarski, Jozef J. Nagy, Peter D. Flasinski, Stanislaw |
author_sort | Bujarski, Jozef J. |
collection | PubMed |
description | It is well known that DNA-based organisms rearrange and repair their genomic DNA through recombination processes, and that these rearrangements serve as a powerful source of variability and adaptation for these organisms. In RNA viruses' genetic recombination is defined as any process leading to the exchange of information between viral RNAs. There are two types of recombination events: legitimate and illegitimate. While legitimate (homologous) recombination occurs between closely related sequences at corresponding positions, illegitimate (nonhomologous) recombination could happen at any position among the unrelated RNA molecules. In order to differentiate between the symmetrical and asymmetrical homologous crosses, Lai defined the former as homologous recombination and the latter as aberrant homologous recombination. This chapter uses brome mosaic virus (BMV), a multicomponent plant RNA virus, as an example to discuss the progress in studying the mechanism of genetic recombination in positive-stranded RNA viruses. Studies described in this chapter summarize the molecular approaches used to increase the frequency of recombination among BMV RNA segments and, more importantly, to target the sites of crossovers to specific BMV RNA regions. It demonstrates that the latter can be accomplished by introducing local complementarities to the recombining substrates. |
format | Online Article Text |
id | pubmed-7131656 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1994 |
publisher | Academic Press Inc. Published by Elsevier Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-71316562020-04-08 Molecular Studies of Genetic RNA–RNA Recombination in Brome Mosaic Virus Bujarski, Jozef J. Nagy, Peter D. Flasinski, Stanislaw Adv Virus Res Article It is well known that DNA-based organisms rearrange and repair their genomic DNA through recombination processes, and that these rearrangements serve as a powerful source of variability and adaptation for these organisms. In RNA viruses' genetic recombination is defined as any process leading to the exchange of information between viral RNAs. There are two types of recombination events: legitimate and illegitimate. While legitimate (homologous) recombination occurs between closely related sequences at corresponding positions, illegitimate (nonhomologous) recombination could happen at any position among the unrelated RNA molecules. In order to differentiate between the symmetrical and asymmetrical homologous crosses, Lai defined the former as homologous recombination and the latter as aberrant homologous recombination. This chapter uses brome mosaic virus (BMV), a multicomponent plant RNA virus, as an example to discuss the progress in studying the mechanism of genetic recombination in positive-stranded RNA viruses. Studies described in this chapter summarize the molecular approaches used to increase the frequency of recombination among BMV RNA segments and, more importantly, to target the sites of crossovers to specific BMV RNA regions. It demonstrates that the latter can be accomplished by introducing local complementarities to the recombining substrates. Academic Press Inc. Published by Elsevier Inc. 1994 2008-02-28 /pmc/articles/PMC7131656/ /pubmed/8191956 http://dx.doi.org/10.1016/S0065-3527(08)60051-2 Text en © 1994 Academic Press Inc. 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 Bujarski, Jozef J. Nagy, Peter D. Flasinski, Stanislaw Molecular Studies of Genetic RNA–RNA Recombination in Brome Mosaic Virus |
title | Molecular Studies of Genetic RNA–RNA Recombination in Brome Mosaic Virus |
title_full | Molecular Studies of Genetic RNA–RNA Recombination in Brome Mosaic Virus |
title_fullStr | Molecular Studies of Genetic RNA–RNA Recombination in Brome Mosaic Virus |
title_full_unstemmed | Molecular Studies of Genetic RNA–RNA Recombination in Brome Mosaic Virus |
title_short | Molecular Studies of Genetic RNA–RNA Recombination in Brome Mosaic Virus |
title_sort | molecular studies of genetic rna–rna recombination in brome mosaic virus |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7131656/ https://www.ncbi.nlm.nih.gov/pubmed/8191956 http://dx.doi.org/10.1016/S0065-3527(08)60051-2 |
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