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Characterisation of cyclin D1 down-regulation in coronavirus infected cells.

Identifieur interne : 003756 ( Main/Exploration ); précédent : 003755; suivant : 003757

Characterisation of cyclin D1 down-regulation in coronavirus infected cells.

Auteurs : Sally M. Harrison [Royaume-Uni] ; Brian K. Dove ; Lisa Rothwell ; Pete Kaiser ; Ian Tarpey ; Gavin Brooks ; Julian A. Hiscox

Source :

RBID : pubmed:17359980

Descripteurs français

English descriptors

Abstract

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.

DOI: 10.1016/j.febslet.2007.02.039
PubMed: 17359980


Affiliations:


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Le document en format XML

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<term>Cyclin D1 (analysis)</term>
<term>Cyclin D1 (genetics)</term>
<term>Cyclin D1 (metabolism)</term>
<term>Down-Regulation</term>
<term>Infectious bronchitis virus</term>
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<term>Cycline D1 (analyse)</term>
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<term>Cycline D1 (métabolisme)</term>
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<term>Régulation négative</term>
<term>Technique de Western</term>
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<div type="abstract" xml:lang="en">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.</div>
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