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Journal of Virology, August 1999, p. 6791-6799, Vol. 73, No. 8
0022-538X/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
Simian Virus 40 Large T Antigen J Domain and Rb-Binding Motif
Are Sufficient To Block Apoptosis Induced by Growth Factor
Withdrawal in a Neural Stem Cell Line
Alison
Slinskey,1
David
Barnes,2 and
James M.
Pipas1,*
Department of Biological Sciences, University
of Pittsburgh, Pittsburgh, Pennsylvania 15260,1
and American Type Culture Collection, Manassas, Virginia
201102
Received 5 February 1999/Accepted 20 April 1999
Serum-free mouse embryo (SFME) cells are a neural stem cell line
that is dependent upon epidermal growth factor (EGF) for survival.
Removal of EGF results in the G1 arrest and apoptosis of
SFME cells. We have shown that the expression of simian virus 40 large
T antigen in SFME cells blocks apoptosis and allows cell survival and
division in the absence of EGF. Therefore the presence of T antigen
abrogates the EGF requirement. The steady-state levels of p53, p21, and
mdm-2 do not increase as SFME cells undergo apoptosis upon EGF
withdrawal. Furthermore, the amino-terminal 136 amino acids (N136) of T
antigen are sufficient to block death and to promote proliferation in
the absence of EGF, while the carboxy-terminal fragment (C251-708),
which contains the p53 binding site, is unable to block death. Taken
together, these data suggest that SFME cells deprived of EGF undergo
p53-independent apoptosis. Mutations that disrupt either the J domain
or Rb family binding abolish the ability of T antigen to block SFME
cell apoptosis and to promote cell growth. We conclude that T antigen
must act on one or more members of the Rb family to inhibit SFME cell apoptosis.
*
Corresponding author. Mailing address: Department of
Biological Sciences, University of Pittsburgh, A234 Langley Hall,
Pittsburgh, PA 15260. Phone: (412) 624-4691. Fax: (412) 624-4759. E-mail: pipas+{at}pitt.edu.
Journal of Virology, August 1999, p. 6791-6799, Vol. 73, No. 8
0022-538X/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
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