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J Virol, March 1998, p. 2532-2537, Vol. 72, No. 3
Department of Tumor Virology, Research
Institute for Microbial Diseases, Osaka University, Osaka 565, Japan
Received 2 September 1997/Accepted 6 December 1997
Previously, we isolated a novel gene, drs, which was
downregulated by retroviral oncogenes such as v-src and
v-K-ras, from a cDNA library of primary rat embryo
fibroblasts. Experiments using a temperature-sensitive mutant of the
v-src gene indicated that downregulation of drs
mRNA was dependent on functional expression of v-Src. In addition,
expression of drs mRNA was also reduced by serum
stimulation of G0-arrested normal rat fibroblast cells. To
clarify the function of the drs gene in cell transformation and proliferation, we introduced drs linked to a potent
promoter into a normal rat cell line, F2408, and examined the effect of ectopic expression of exogenous drs on the transformation
by the v-src gene and growth properties. Cells expressing
exogenous drs gene showed significantly decreased
efficiency of transformation by v-src irrespective of
functional expression of v-Src kinase, while the growth rate and
G1/S progression of the cells were not suppressed by
expression of exogenous drs gene, indicating that drs has the ability to suppress v-src
transformation without disturbing cell proliferation.
0022-538X/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.
Suppression of v-src Transformation by
the drs Gene
*
Corresponding author. Mailing address: Department of
Tumor Virology, Research Institute for Microbial Diseases, Osaka
University, 3-1 Yamadaoka, Suita, Osaka 565, Japan. Phone:
81-6-879-8313. Fax: 81-6-879-8315. E-mail:
hiroinou{at}biken.osaka-u.ac.jp.
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