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PMID: 9168886 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S. Research Support, U.S. Gov't, P.H.S.

Inhibition of cellular Cdk2 activity blocks human cytomegalovirus replication.

Virology ·Vol. 231 ·No. 2 ·1997-05-12 ·Pages 239-47

Bresnahan WA, Boldogh I, Chi P, Thompson EA, Albrecht T

Abstract

Human cytomegalovirus is a herpesvirus that induces numerous cellular processes upon infection. Among these are activation of cyclin-dependent kinase 2, which regulates cell cycle progression in G1 and S phase. We report here that inhibition of cellular Cdk2 activity blocks HCMV replication. Inhibition of Cdk2 activity by roscovitine inhibits HCMV DNA synthesis, production of infectious progeny, and late antigen expression in infected cells in a dose-dependent manner. HCMV replication is also inhibited by the expression of a Cdk2 dominant negative mutant, whereas expression of wild-type Cdk2 has no effect on viral replication. These data indicate that activation of cellular Cdk2 is necessary for HCMV replication.

MeSH Terms
Antigens, Viral/biosynthesis CDC2-CDC28 Kinases Cell Line Cyclin-Dependent Kinase 2 Cyclin-Dependent Kinases/antagonists & inhibitors Cyclins/metabolism Cytomegalovirus/growth & development Enzyme Activation Enzyme Inhibitors/pharmacology Fluorescent Antibody Technique, Indirect Humans Protein Serine-Threonine Kinases/antagonists & inhibitors Purines/pharmacology Roscovitine Virus Replication/drug effects
Chemicals
Antigens, Viral Cyclins Enzyme Inhibitors Purines Roscovitine Protein Serine-Threonine Kinases CDC2-CDC28 Kinases CDK2 protein, human Cyclin-Dependent Kinase 2 Cyclin-Dependent Kinases
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Bresnahan W A
Department of Microbiology and Immunology, University of Texas Medical Branch, Galveston 77550, USA.
Boldogh I
Chi P
Thompson E A
Albrecht T
Article Info
Journal
Virology
Abbr.
Virology
ISSN
0042-6822
Published
1997-05-12
Pages
239-47
Language
English
Region
United States
NLM ID
0110674
Subset
IM
Grants
NIA NIH HHS · AG10514 · United States
NCI NIH HHS · CA24347 · United States
NIDCR NIH HHS · DE11389 · United States
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