Protein IE1 is the product of a baculovirus gene, ie1, that is activat
ed immediately upon entrance of the viral genome into the cell nucleus
. This protein was previously shown to be a trans-regulator of viral g
enes whose products are required for initiation of the infectious cycl
e including viral DNA replication. To test whether the IE1 protein is
also capable of trans-regulating nuclear genes of the host in vitro an
d in vivo, we transfected the ie1 gene of Bombyx mori nuclear polyhedr
osis virus (BmNPV) into silkworm Bm5 tissue culture cells together wit
h expression cassettes directing expression of chloramphenicol acetyl
transferase or juvenile hormone esterase under the control of the cyto
plasmic actin A3 gene promoter of B. mori. Cotransfection with the ie1
gene resulted in a dramatic increase in the amount of the two enzymes
expressed in the transfected cells. The increased enzyme activities c
orrelate with an increased accumulation of the corresponding mRNAs, an
d the latter is caused by an increase in the rate of transcription dir
ected by the cytoplasmic actin gene promoter. The chromosomal cytoplas
mic actin gene of Bm5 cells is also upregulated upon transfection of t
he cells with the ie1 gene. However, infection of cells with BmNPV doe
s not cause an increase in the level of expression of the endogenous c
ytoplasmic actin gene. Thus, the effect of IE1 on the transcriptional
properties of the cytoplasmic actin gene vary depending on whether IE1
is expressed in isolation or in the context of a viral infection. The
trans-activating effects of BmNPV ie1 gene expression on the silkmoth
actin promoter are also evident in Spodoptera frugiperda Sf21 and Cho
ristoneura fumiferana Cf1 tissue culture cells. Finally, the ie1 gene
of Autographa californica nuclear polyhedrosis virus can substitute fo
r its BmNPV counterpart in all cell lines tested. (C) 1996 Academic Pr
ess, Inc.