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Identification of Plant Virus IRES

Plant RNA viruses exploit nonorthodox strategies, such as the use of internal ribosomal entry sites (IRES), to express multiple genes from a single RNA species. IRES elements have been reported in tobacco etch virus (TEV), crucifer infecting tobamovirus (crTMV), hibiscus chlorotic ringspot virus (HC...

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Detalles Bibliográficos
Autores principales: Wong, Sek-Man, Koh, Dora Chin-Yen, Liu, Dingxiang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7121985/
https://www.ncbi.nlm.nih.gov/pubmed/18370252
http://dx.doi.org/10.1007/978-1-59745-102-4_9
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author Wong, Sek-Man
Koh, Dora Chin-Yen
Liu, Dingxiang
author_facet Wong, Sek-Man
Koh, Dora Chin-Yen
Liu, Dingxiang
author_sort Wong, Sek-Man
collection PubMed
description Plant RNA viruses exploit nonorthodox strategies, such as the use of internal ribosomal entry sites (IRES), to express multiple genes from a single RNA species. IRES elements have been reported in tobacco etch virus (TEV), crucifer infecting tobamovirus (crTMV), hibiscus chlorotic ringspot virus (HCRSV), and many other animal and plant RNA viruses. In this chapter, the methodology used to identify and characterize a plant virus IRES element, including construction of a translation reporter vector for testing the IRES activity, testing the IRES activity in coupled in vitro transcription and translation systems and mammalian cells analysis of RNA stability, and sucrose gradient analysis and polysome profiling, is presented.
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spelling pubmed-71219852020-04-06 Identification of Plant Virus IRES Wong, Sek-Man Koh, Dora Chin-Yen Liu, Dingxiang Plant Virology Protocols Article Plant RNA viruses exploit nonorthodox strategies, such as the use of internal ribosomal entry sites (IRES), to express multiple genes from a single RNA species. IRES elements have been reported in tobacco etch virus (TEV), crucifer infecting tobamovirus (crTMV), hibiscus chlorotic ringspot virus (HCRSV), and many other animal and plant RNA viruses. In this chapter, the methodology used to identify and characterize a plant virus IRES element, including construction of a translation reporter vector for testing the IRES activity, testing the IRES activity in coupled in vitro transcription and translation systems and mammalian cells analysis of RNA stability, and sucrose gradient analysis and polysome profiling, is presented. 2008 /pmc/articles/PMC7121985/ /pubmed/18370252 http://dx.doi.org/10.1007/978-1-59745-102-4_9 Text en © Humana Press, a part of Springer Science + Business Media, LLC 2008 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic.
spellingShingle Article
Wong, Sek-Man
Koh, Dora Chin-Yen
Liu, Dingxiang
Identification of Plant Virus IRES
title Identification of Plant Virus IRES
title_full Identification of Plant Virus IRES
title_fullStr Identification of Plant Virus IRES
title_full_unstemmed Identification of Plant Virus IRES
title_short Identification of Plant Virus IRES
title_sort identification of plant virus ires
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7121985/
https://www.ncbi.nlm.nih.gov/pubmed/18370252
http://dx.doi.org/10.1007/978-1-59745-102-4_9
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