Infection with vaccinia virus alters regulation of cell cycle progression.

Abstract

The effect of vaccinia virus (VV) on cell cycle progression and its regulators was studied. Infected cultures showed significantly increased transit through G1, decreasing the percentage of cells in G1 and increasing the percentage in S phase. The numbers of cells in G2/M were not affected. Because of the increased S-phase fraction at the expense of G1, expression of cyclins and cyclin-dependent kinases (Cdks) that regulate cell cycle checkpoints was examined. Transcripts for cyclins A and B, Cdk2, and Cdc2 were decreased in VV-infected cells as infection progressed. The amounts of p53 and p27 proteins decreased after 12 and 24 h of infection, respectively. The Cdc2 and Cdk2 protein levels were decreased with increasing time after infection. Taken together, these findings would be expected to lead to more cells in S phase and G2/M, as was observed. Therefore, VV actively modulates expression of cellular regulators of the cell cycle and alters cell cycle progression.

• Authors: A Wali, D S Strayer
• Journal: DNA and cell biology (DNA Cell Biol) Vol. 18 Issue 11 Pg. 837-43 (Nov 1999) ISSN: 1044-5498 [Print] United States
• PMID: 10595397 (Publication Type: Journal Article, Research Support, U.S. Gov't, P.H.S.)

Chemical References

• Cell Cycle Proteins
• Cyclin B
• Microfilament Proteins
• Muscle Proteins
• RNA, Messenger
• Tagln protein, mouse
• Tumor Suppressor Protein p53
• CDC2 Protein Kinase
• Cyclin-Dependent Kinases

Topics

• Animals
• CDC2 Protein Kinase (metabolism)
• Cell Cycle (physiology)
• Cell Cycle Proteins (metabolism)
• Cell Line
• Cyclin B (analysis, metabolism)
• Cyclin-Dependent Kinases (metabolism)
• Genes, cdc (physiology)
• Microfilament Proteins (metabolism)
• Muscle Proteins
• RNA, Messenger (metabolism)
• Rabbits
• Tumor Suppressor Protein p53 (metabolism)
• Vaccinia virus (metabolism)