In all sequenced herpesvirus genomes, a homolog of the herpes simplex virus
type 1 UL15 gene has been identified. This gene encodes a protein that is
involved in viral genome maturation. Although transcription of the alphaher
pesvirus UL15 gene has been analyzed in detail, not much is known about the
expression of its betaherpesvirus homologs. We therefore set out to charac
terize transcription of the rat cytomegalovirus counterpart of UL15, R89. H
ere we report that R89 consists of two exons separated by a 4.7-kb intron.
The spliced R89 transcript, which is expressed at late times postinfection
(p.i.), has the capacity to encode a protein of 670 amino acids with a calc
ulated molecular mass of 77.1 kDa. The predicted amino acid sequence of thi
s protein is highly similar to that of the proteins predicted to be encoded
by the human cytomegalovirus UL89 and murine cytomegalovirus M89 genes (64
.3 and 84.5% overall identity, respectively). The region between R89 exon 1
and exon 2 was found to contain five additional genes, r90, R91, R92, R93
and R94, the latter two of which are conserved among all herpesviruses. We
show that these genes are transcribed in a highly complex fashion, resultin
g in numerous mono- and polycistronic mRNAs. (C) 2000 Published by Elsevier
Science B.V.