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1.
PLoS One ; 8(2): e57340, 2013.
Article in English | MEDLINE | ID: mdl-23437375

ABSTRACT

Adenoviruses (Ads) with deletion of E1b55K preferentially replicate in cancer cells and have been used in cancer therapies. We have previously shown that Ad E1B55K protein is involved in induction of cyclin E for Ad replication, but this E1B55K function is not required in cancer cells in which deregulation of cyclin E is frequently observed. In this study, we investigated the interaction of cyclin E and CDK2 in Ad-infected cells. Ad infection significantly increased the large form of cyclin E (cyclin EL), promoted cyclin E/CDK2 complex formation and increased CDK2 phosphorylation at the T160 site. Activated CDK2 caused pRb phosphorylation at the S612 site. Repression of CDK2 activity with the chemical inhibitor roscovitine or with specific small interfering RNAs significantly decreased pRb phosphorylation, with concomitant repression of viral replication. Our results suggest that Ad-induced cyclin E activates CDK2 that targets the transcriptional repressor pRb to generate a cellular environment for viral productive replication. This study reveals a new molecular basis for oncolytic replication of E1b-deleted Ads and will aid in the development of new strategies for Ad oncolytic virotherapies.


Subject(s)
Adenoviridae/genetics , Cyclin E/genetics , Cyclin-Dependent Kinase 2/genetics , Gene Expression Regulation, Neoplastic/drug effects , Oncogene Proteins/genetics , Retinoblastoma Protein/genetics , Viral Proteins/genetics , Adenoviridae/metabolism , Cell Line, Tumor , Cyclin E/agonists , Cyclin E/metabolism , Cyclin-Dependent Kinase 2/antagonists & inhibitors , Cyclin-Dependent Kinase 2/metabolism , Fibroblasts/drug effects , Fibroblasts/metabolism , Fibroblasts/virology , Genes, Reporter , Green Fluorescent Proteins , HEK293 Cells , Host-Pathogen Interactions , Humans , Oncogene Proteins/agonists , Oncogene Proteins/metabolism , Phosphorylation , Protein Kinase Inhibitors/pharmacology , Purines/pharmacology , RNA, Small Interfering/genetics , Retinoblastoma Protein/antagonists & inhibitors , Retinoblastoma Protein/metabolism , Roscovitine , Viral Proteins/metabolism , Virus Replication/drug effects
2.
Mol Cell ; 23(2): 149-50, 2006 Jul 21.
Article in English | MEDLINE | ID: mdl-16857579

ABSTRACT

Targeting proteins for irreversible degradation must be under tight control and is often regulated at the level of substrate-receptor binding. But does a protein really need to be marked twice with two different modifications, first phosphorylation and then isomerization, to bind its receptor, as van Drogen et al. (2006) show for cyclin E?


Subject(s)
Cyclin E/agonists , Cyclin E/metabolism , Ubiquitins/metabolism , Cell Cycle Proteins/metabolism , F-Box Proteins/metabolism , Isomerism , Phosphorylation , Protein Binding , Ubiquitin-Protein Ligases/metabolism
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