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Journal of Virology, January 2000, p. 523-528, Vol. 74, No. 1
The Marjorie B. Kovler Viral Oncology
Laboratories, The University of Chicago, Chicago, Illinois 60637
Received 5 August 1999/Accepted 1 October 1999
The herpes simplex virus 1 UL3 and UL4 open
reading frames are expressed late in infection and are not essential
for viral replication in cultured cells in vitro. An earlier report
showed that the UL4 protein colocalizes with the products
of the
0022-538X/0/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.
Small Dense Nuclear Bodies Are the Site of
Localization of Herpes Simplex Virus 1 UL3 and
UL4 Proteins and of ICP22 Only When the Latter Protein
Is Present
22/US1.5 genes in small nuclear dense bodies.
Here we report that the UL3 protein also colocalized in
these small nuclear dense bodies and the localization of
UL3 and UL4 proteins in these bodies required the presence of
22/US1.5 genes. In cells infected with a
mutant lacking intact
22/US1.5 genes, UL3
was diffused throughout the nucleus even though the overall
accumulation of the
2 UL3 protein was decreased. The
results suggest that ICP22 acts both as a regulator of UL3
accumulation and as the structural component and anchor of these small
dense nuclear bodies.
*
Corresponding author. Mailing address: The Marjorie B. Kovler Viral Oncology Laboratories, The University of Chicago, 910 E. 58th St., Chicago, IL 60637. Phone: (773) 702-1898. Fax: (773) 702-1631. E-mail: bernard{at}cummings.uchicago.edu.
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