Gr. Sandford et al., CHARACTERIZATION OF THE MAJOR LOCUS OF IMMEDIATE-EARLY GENES OF RAT CYTOMEGALOVIRUS, Journal of virology, 67(7), 1993, pp. 4093-4103
A major locus of rat cytomegalovirus (RCMV) immediate-early (IE) RNA t
ranscription was identified. A cDNA library from rat embryo fibroblast
s infected with RCMV under IE conditions was constructed and screened
by using appropriate RCMV DNA probes, revealing at least two IE genes
(IE1 and IE2) transcribed from this locus by differential splicing. Th
e first three exons (the first is noncoding) are spliced to exon 4 to
form IE1 and to exon 5 to form IE2. The structural organization of the
RCNIV major IE region is therefore similar to that of human cytomegal
ovirus (HCMV) and murine cytomegalovirus (MCMV). When we compared the
predicted amino acid sequences of the IE1 proteins of RCMV, HCMV, and
MCMV, no areas of homology were found across all three proteins, while
a few small areas of homology were found between RCMV IE1 and MCMV IE
1. In contrast, large areas of homology were found across the carboxyl
half of RCMV IE2, HCMV IE2, and MCMV ie3 proteins. In addition, simil
arities were found at the beginning of exon 5 of RCMV and MCMV. The po
ssible significance of these conserved regions is discussed. Dinucleot
ide frequency analysis demonstrated a decrease in CpG frequency over t
he IE region. The IE gene products were able to transactivate heterolo
gous promoters.