Abstract
The U L 15 gene of herpes simplex virus (HSV) is one of several genes required for the packaging of viral DNA into intranuclear B capsids to produce C capsids that become enveloped at the inner nuclear membrane. A rabbit antiserum directed against U L 15-encoded protein recognized three proteins with apparent M r s of 79,000, 80,000, and 83,000 in highly purified B capsids. The 83,000- M r protein was detected in type C capsids and comigrated with the product of a U L 15 cDNA transcribed and translated in vitro. The 83,000- and 80,000- M r proteins were readily detected in purified virions. Inasmuch as (i) none of these proteins were detectable in capsids purified from cells infected with HSV-1(ΔU L 15), a virus lacking an intact U L 15 gene, and (ii) corresponding proteins in capsids purified from cells infected with a recombinant virus [HSV-1(R7244), containing a 20-codon tag at the 3′ end of U L 15] were decreased in electrophoretic mobility relative to the wild-type proteins, we conclude that the proteins with apparent M r s of 83,000, 80,000, and 79,000 are products of U L 15 with identical C termini. The 79,000-, 80,000-, and 83,000- M r proteins remained associated with B capsids in the presence of 0.5 M guanidine HCl and remained detectable in capsids treated with 2.0 M guanidine HCl and lacking proteins associated with the capsid core. These data, therefore, indicate that U L 15-encoded proteins are integral components of B capsids. Only the 83,000- M r protein was detected in B capsids purified from cells infected with viruses lacking the U L 6, U L 17, or U L 28 genes, which are required for DNA cleavage and packaging, suggesting that capsid association of the 80,000- and 79,000- M r proteins requires intact cleavage and packaging machinery. These data, therefore, indicate that capsid association of the 80,000- and 79,000- M r U L 15-encoded proteins reflects a previously unrecognized step in the DNA cleavage and packaging reaction.