Characterisation of cyclin D1 down-regulation in coronavirus infected cells.
Identifieur interne : 003756 ( Main/Exploration ); précédent : 003755; suivant : 003757Characterisation 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. HiscoxSource :
- FEBS letters [ 0014-5793 ] ; 2007.
Descripteurs français
- KwdFr :
- MESH :
- analyse : ARN messager, ARN viral, Cycline D1.
- génétique : Cycline D1.
- métabolisme : ARN messager, ARN viral, Cycline D1.
- Animaux, Cellules Vero, Coronavirus, RT-PCR, Régulation négative, Technique de Western, Virus de la bronchite infectieuse.
English descriptors
- KwdEn :
- Animals, Blotting, Western, Chlorocebus aethiops, Coronavirus, Cyclin D1 (analysis), Cyclin D1 (genetics), Cyclin D1 (metabolism), Down-Regulation, Infectious bronchitis virus, RNA, Messenger (analysis), RNA, Messenger (metabolism), RNA, Viral (analysis), RNA, Viral (metabolism), Reverse Transcriptase Polymerase Chain Reaction, Vero Cells.
- MESH :
- chemical , analysis : Cyclin D1, RNA, Messenger, RNA, Viral.
- chemical , genetics : Cyclin D1.
- chemical , metabolism : Cyclin D1, RNA, Messenger, RNA, Viral.
- Animals, Blotting, Western, Chlorocebus aethiops, Coronavirus, Down-Regulation, Infectious bronchitis virus, Reverse Transcriptase Polymerase Chain Reaction, Vero Cells.
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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<front><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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