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Characterisation of cyclin D1 down‐regulation in coronavirus infected cells

The positive strand RNA coronavirus, infectious bronchitis virus (IBV), induces a G2/M phase arrest and reduction in the G1 and G1/S phase transition regulator cyclin D1. Quantitative real‐time RT‐PCR and Western blot analysis demonstrated that cyclin D1 was reduced post‐transcriptionally within inf...

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Autores principales: Harrison, Sally M., Dove, Brian K., Rothwell, Lisa, Kaiser, Pete, Tarpey, Ian, Brooks, Gavin, Hiscox, Julian A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7094712/
https://www.ncbi.nlm.nih.gov/pubmed/17359980
http://dx.doi.org/10.1016/j.febslet.2007.02.039
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author Harrison, Sally M.
Dove, Brian K.
Rothwell, Lisa
Kaiser, Pete
Tarpey, Ian
Brooks, Gavin
Hiscox, Julian A.
author_facet Harrison, Sally M.
Dove, Brian K.
Rothwell, Lisa
Kaiser, Pete
Tarpey, Ian
Brooks, Gavin
Hiscox, Julian A.
author_sort Harrison, Sally M.
collection PubMed
description The positive strand RNA coronavirus, infectious bronchitis virus (IBV), induces a G2/M phase arrest and reduction in the G1 and G1/S phase transition regulator cyclin D1. Quantitative real‐time RT‐PCR and Western blot analysis demonstrated that cyclin D1 was reduced post‐transcriptionally within infected cells independently of the cell‐cycle stage at the time of infection. Confocal microscopy revealed that cyclin D1 decreased in IBV‐infected cells as infection progressed and inhibition studies indicated that a population of cyclin D1 could be targeted for degradation by a virus mediated pathway. In contrast to the SARS‐coronavirus, IBV nucleocapsid protein did not interact with cyclin D1.
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spelling pubmed-70947122020-03-25 Characterisation of cyclin D1 down‐regulation in coronavirus infected cells Harrison, Sally M. Dove, Brian K. Rothwell, Lisa Kaiser, Pete Tarpey, Ian Brooks, Gavin Hiscox, Julian A. FEBS Lett Short Communications The positive strand RNA coronavirus, infectious bronchitis virus (IBV), induces a G2/M phase arrest and reduction in the G1 and G1/S phase transition regulator cyclin D1. Quantitative real‐time RT‐PCR and Western blot analysis demonstrated that cyclin D1 was reduced post‐transcriptionally within infected cells independently of the cell‐cycle stage at the time of infection. Confocal microscopy revealed that cyclin D1 decreased in IBV‐infected cells as infection progressed and inhibition studies indicated that a population of cyclin D1 could be targeted for degradation by a virus mediated pathway. In contrast to the SARS‐coronavirus, IBV nucleocapsid protein did not interact with cyclin D1. John Wiley and Sons Inc. 2007-04-03 2007-02-28 /pmc/articles/PMC7094712/ /pubmed/17359980 http://dx.doi.org/10.1016/j.febslet.2007.02.039 Text en FEBS Letters 581 (2007) 1873-3468 © 2015 Federation of European Biochemical Societies This article is being made freely available through PubMed Central as part of the COVID-19 public health emergency response. It can be used for unrestricted research re-use and analysis in any form or by any means with acknowledgement of the original source, for the duration of the public health emergency.
spellingShingle Short Communications
Harrison, Sally M.
Dove, Brian K.
Rothwell, Lisa
Kaiser, Pete
Tarpey, Ian
Brooks, Gavin
Hiscox, Julian A.
Characterisation of cyclin D1 down‐regulation in coronavirus infected cells
title Characterisation of cyclin D1 down‐regulation in coronavirus infected cells
title_full Characterisation of cyclin D1 down‐regulation in coronavirus infected cells
title_fullStr Characterisation of cyclin D1 down‐regulation in coronavirus infected cells
title_full_unstemmed Characterisation of cyclin D1 down‐regulation in coronavirus infected cells
title_short Characterisation of cyclin D1 down‐regulation in coronavirus infected cells
title_sort characterisation of cyclin d1 down‐regulation in coronavirus infected cells
topic Short Communications
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7094712/
https://www.ncbi.nlm.nih.gov/pubmed/17359980
http://dx.doi.org/10.1016/j.febslet.2007.02.039
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