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J Gen Virol 73 (1992), 531-538; DOI 10.1099/0022-1317-73-3-531
© 1992 Society for General Microbiology

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On the cellular localization of the components of the herpes simplex virus type 1 helicase-primase complex and the viral origin-binding protein

Janice M. Calder, Elizabeth C. Stow and Nigel D. Stow

Medical Research Council Virology Unit, Institute of Virology, Church Street, Glasgow G11 5JR, U.K.

We constructed recombinant viruses based on the herpes simplex virus type 1 mutant tsK which individually were able to express the products of four viral DNA replication genes (UL5, UL8, UL9 and UL52) in the absence of any of the other proteins required for viral DNA synthesis. These viruses were used in immunofluorescence experiments to investigate the cellular localization of the four replication proteins expressed. The results demonstrated that all three components of the viral helicase-primase complex (UL5, UL8 and UL52 proteins) must be co-expressed to allow their efficient localization to the nucleus. Since the UL5 and UL52 proteins together form a complex which is enzymatically indistinguishable from a complex formed from all three proteins, a possible role of the UL8 protein may be in facilitating nuclear uptake. The UL9 protein (origin-binding protein) efficiently entered the cell nucleus when expressed alone. Both UL9 protein and the tripartite helicase-primase complex exhibited patterns of fluorescence which resembled the ‘pre-replicative sites’ described previously.

Received 2 September 1991; accepted 20 November 1991.


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