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J Virol, January 1998, p. 684-692, Vol. 72, No. 1
0022-538X/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.
Role of Baculovirus IE2 and Its RING Finger in
Cell Cycle Arrest
Elena A.
Prikhod'ko and
Lois K.
Miller*
Departments of Entomology and Genetics, The
University of Georgia, Athens, Georgia 30602
Received 2 June 1997/Accepted 1 October 1997
The ie2 gene of Autographa californica
nuclear polyhedrosis virus (AcMNPV) is known to
transactivate transient expression from viral promoters in a host
cell-specific manner. We report that transfection of
Spodoptera frugiperda (SF-21) cells with ie2
was sufficient to arrest the cell cycle, resulting in the accumulation
of enlarged cells with abnormally high DNA contents. By 72 h
posttransfection, more than 50% of ie2-transfected
cells had DNA contents greater than 4N. There was no evidence of
mitotic spindle formation in these cells, and expression of
ie2 appeared to block cell cycle progression in S phase.
Several ie2 mutants were analyzed to further define the
region of IE2 responsible for arresting the cell cycle. Analysis of
these mutants showed that deletion of the RING finger motif eliminated
the ability of IE2 to arrest the cell cycle but did not affect its
ability to transactivate the ie1 promoter. Moreover,
mutation of a single conserved cysteine (C251) of the RING finger motif
abolished the ability of IE2 to block cell cycle progression but had no
apparent effect on its trans-regulatory activity. In
contrast, a mutant of IE2 containing a deletion of residues 94 to 173 was able to block cell division but lacked trans-regulatory
activity. Thus, the ability of IE2 to arrest the cell cycle depended on
the integrity of the RING finger motif and was distinct from and
independent of its ability to trans-activate the
ie1 promoter. IE2 also arrested the division of cells
derived from other insect species, Trichoplusia ni (TN-368
and BTI-TN-5B1-4) and Helicoverpa zea (Hz-AM1).
*
Corresponding author. Mailing address: Department of
Entomology, The University of Georgia, 413 Biological Sciences
Building, Athens, GA 30602-2603. Phone: (706) 542-2294. Fax: (706)
542-2279. E-mail: Miller{at}bscr.uga.edu.
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