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Journal of Virology, August 2001, p. 7429-7434, Vol. 75, No. 16
0022-538X/01/$04.00+0 DOI: 10.1128/JVI.75.16.7429-7434.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.
Reovirus-Induced
1s-Dependent G2/M
Phase Cell Cycle Arrest Is Associated with Inhibition of
p34cdc2
George J.
Poggioli,1
Terence S.
Dermody,2,3,4 and
Kenneth L.
Tyler1,5,6,7,8,*
Departments of
Neurology,5
Medicine,6
Microbiology,1 and
Immunology,7 University of
Colorado Health Sciences Center, and Neurology Service, Denver Veterans
Affairs Medical Center,8 Denver, Colorado 80220, and Departments of Pediatrics2 and
Microbiology and Immunology3 and
Elizabeth B. Lamb Center for Pediatric
Research,4 Vanderbilt University School of
Medicine, Nashville, Tennessee 37232
Received 28 February 2001/Accepted 23 May 2001
Serotype 3 reoviruses inhibit cellular proliferation by inducing a
G2/M phase cell cycle arrest. Reovirus-induced
G2/M phase arrest requires the viral S1 gene-encoded
1s
nonstructural protein. The G2-to-M transition represents a
cell cycle checkpoint that is regulated by the kinase
p34cdc2. We now report that infection with serotype 3 reovirus strain Abney, but not serotype 1 reovirus strain Lang, is
associated with inhibition and hyperphosphorylation of
p34cdc2. The
1s protein is necessary and sufficient for
inhibitory phosphorylation of p34cdc2, since a viral mutant
lacking
1s fails to hyperphosphorylate p34cdc2 and
inducible expression of
1s is sufficient for p34cdc2
hyperphosphorylation. These studies establish a mechanism by which
reovirus can perturb cell cycle regulation.
*
Corresponding author. Mailing address: Department of
Neurology (B-182), University of Colorado Health Sciences Center, 4200 E. 9th Ave., Denver, CO 80262. Phone: (303) 393-2874. Fax: (303) 393-4686. E-mail: Ken.Tyler{at}UCHSC.edu.
Journal of Virology, August 2001, p. 7429-7434, Vol. 75, No. 16
0022-538X/01/$04.00+0 DOI: 10.1128/JVI.75.16.7429-7434.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.
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