Promotion of Viral IRES-Mediated Translation Initiation under Mild Hypothermia.

Internal ribosome entry site (IRES)-mediated translation is an essential replication step for certain viruses. As IRES-mediated translation is regulated differently from cap-dependent translation under various cellular conditions, we sought to investigate whether temperature influences efficiency of...

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Main Authors: Maria Licursi, Ricardo A Carmona-Martinez, Seyd Razavi, Kensuke Hirasawa
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2015-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC4423848?pdf=render
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spelling doaj-3b4b571318e84163a218af335f4124702020-11-24T21:24:28ZengPublic Library of Science (PLoS)PLoS ONE1932-62032015-01-01105e012617410.1371/journal.pone.0126174Promotion of Viral IRES-Mediated Translation Initiation under Mild Hypothermia.Maria LicursiRicardo A Carmona-MartinezSeyd RazaviKensuke HirasawaInternal ribosome entry site (IRES)-mediated translation is an essential replication step for certain viruses. As IRES-mediated translation is regulated differently from cap-dependent translation under various cellular conditions, we sought to investigate whether temperature influences efficiency of viral IRES-mediated translation initiation by using bicistronic reporter constructs containing an IRES element of encephalomyocarditis virus (EMCV), foot-and-mouth disease virus (FMDV), hepatitis C virus (HCV), human rhinovirus (HRV) or poliovirus (PV). Under mild hypothermic conditions (30 and 35°C), we observed increases in the efficiency of translation initiation by HCV and HRV IRES elements compared to translation initiation at 37°C. The promotion of HRV IRES activity was observed as early as 2 hours after exposure to mild hypothermia. We also confirmed the promotion of translation initiation by HRV IRES under mild hypothermia in multiple cell lines. The expression levels and locations of polypyrimidine tract-binding protein (PTB) and upstream of N-Ras (unr), the IRES trans-acting factors (ITAFs) of HCV and HRV IRES elements, were not modulated by the temperature shift from 37°C to 30°C. Taken together, this study demonstrates that efficiency of translation initiation by some viral IRES elements is temperature dependent.http://europepmc.org/articles/PMC4423848?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Maria Licursi
Ricardo A Carmona-Martinez
Seyd Razavi
Kensuke Hirasawa
spellingShingle Maria Licursi
Ricardo A Carmona-Martinez
Seyd Razavi
Kensuke Hirasawa
Promotion of Viral IRES-Mediated Translation Initiation under Mild Hypothermia.
PLoS ONE
author_facet Maria Licursi
Ricardo A Carmona-Martinez
Seyd Razavi
Kensuke Hirasawa
author_sort Maria Licursi
title Promotion of Viral IRES-Mediated Translation Initiation under Mild Hypothermia.
title_short Promotion of Viral IRES-Mediated Translation Initiation under Mild Hypothermia.
title_full Promotion of Viral IRES-Mediated Translation Initiation under Mild Hypothermia.
title_fullStr Promotion of Viral IRES-Mediated Translation Initiation under Mild Hypothermia.
title_full_unstemmed Promotion of Viral IRES-Mediated Translation Initiation under Mild Hypothermia.
title_sort promotion of viral ires-mediated translation initiation under mild hypothermia.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2015-01-01
description Internal ribosome entry site (IRES)-mediated translation is an essential replication step for certain viruses. As IRES-mediated translation is regulated differently from cap-dependent translation under various cellular conditions, we sought to investigate whether temperature influences efficiency of viral IRES-mediated translation initiation by using bicistronic reporter constructs containing an IRES element of encephalomyocarditis virus (EMCV), foot-and-mouth disease virus (FMDV), hepatitis C virus (HCV), human rhinovirus (HRV) or poliovirus (PV). Under mild hypothermic conditions (30 and 35°C), we observed increases in the efficiency of translation initiation by HCV and HRV IRES elements compared to translation initiation at 37°C. The promotion of HRV IRES activity was observed as early as 2 hours after exposure to mild hypothermia. We also confirmed the promotion of translation initiation by HRV IRES under mild hypothermia in multiple cell lines. The expression levels and locations of polypyrimidine tract-binding protein (PTB) and upstream of N-Ras (unr), the IRES trans-acting factors (ITAFs) of HCV and HRV IRES elements, were not modulated by the temperature shift from 37°C to 30°C. Taken together, this study demonstrates that efficiency of translation initiation by some viral IRES elements is temperature dependent.
url http://europepmc.org/articles/PMC4423848?pdf=render
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AT ricardoacarmonamartinez promotionofviraliresmediatedtranslationinitiationundermildhypothermia
AT seydrazavi promotionofviraliresmediatedtranslationinitiationundermildhypothermia
AT kensukehirasawa promotionofviraliresmediatedtranslationinitiationundermildhypothermia
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