sv40 early region
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Author(s):  
R. Voglauer ◽  
J. Grillari ◽  
K. Fortschegger ◽  
M. Wieser ◽  
T. Sterovsky ◽  
...  


2002 ◽  
Vol 22 (19) ◽  
pp. 6767-6778 ◽  
Author(s):  
Patrick T. Reilly ◽  
Joanna Wysocka ◽  
Winship Herr

ABSTRACT Owing to a single missense mutation in the cell proliferation factor HCF-1, the temperature-sensitive tsBN67 hamster cell line arrests proliferation at nonpermissive temperatures, primarily in a G0/G1 state, and displays temperature-sensitive cytokinesis defects. The HCF-1 mutation in tsBN67 cells also causes a temperature-sensitive dissociation of HCF-1 from chromatin prior to cell proliferation arrest, suggesting that HCF-1-chromatin association is important for mammalian-cell proliferation. Here, we report that the simian virus 40 (SV40) early region, in particular, large T antigen (Tag), and the adenovirus oncoprotein E1A can rescue the tsBN67 cell proliferation defect at nonpermissive temperatures. The SV40 early region rescues the tsBN67 cell proliferation defect without restoring the HCF-1-chromatin association, indicating that these oncoproteins bypass a requirement for HCF-1 function. The SV40 early region also rescues the tsBN67 cytokinesis defect, suggesting that the roles of HCF-1 in cell proliferation and proper cytokinesis are intimately linked. The ability of SV40 Tag and adenovirus E1A to inactivate members of the pRb protein family—pRb, p107, and p130—is important for the bypass of HCF-1 function. These results suggest that HCF-1 regulates mammalian-cell proliferation and cytokinesis, at least in part, by either directly or indirectly opposing pRb family member function.



1995 ◽  
Vol 17 (2) ◽  
pp. 75-81 ◽  
Author(s):  
R. De Silva ◽  
D. G. Zahra ◽  
E. L. Duncan ◽  
R. R. Reddel


1994 ◽  
Vol 34 (3) ◽  
pp. 237-263 ◽  
Author(s):  
Frank J. O'Neill ◽  
Xiaoling Xu ◽  
Yan Gao ◽  
Mark Rosenfeld ◽  
Frank Jenkins ◽  
...  


1994 ◽  
Vol 213 (2) ◽  
pp. 418-427 ◽  
Author(s):  
Ruwani De Silva ◽  
Noel J. Whitaker ◽  
Eileen M. Rogan ◽  
Roger R. Reddel


1994 ◽  
Vol 16 (1) ◽  
pp. 57-60 ◽  
Author(s):  
T. Tokiwa ◽  
M. M. Lipsky ◽  
D. T. Smoot ◽  
J. F. Lechner




1992 ◽  
Vol 25 (3) ◽  
pp. 349-356 ◽  
Author(s):  
O. Hohenwarter ◽  
E. Zinser ◽  
C. Schmatz ◽  
F. Rüker ◽  
H. Katinger


Intervirology ◽  
1991 ◽  
Vol 32 (3) ◽  
pp. 173-184 ◽  
Author(s):  
Alain Legrand ◽  
Maurice Nachtigal


1990 ◽  
Vol 10 (10) ◽  
pp. 5365-5377
Author(s):  
D Wynford-Thomas ◽  
J A Bond ◽  
F S Wyllie ◽  
J S Burns ◽  
E D Williams ◽  
...  

To overcome the difficulty of assessing oncogene action in human epithelial cell types, such as thyroid, which have limited proliferative potential in culture, we have explored the use of temperature-sensitive (ts) mutants of simian virus 40 (SV40) early region to create conditionally immortalized epithelial cell lines. Normal primary cultures of human thyroid follicular cells were transfected with a plasmid containing the SV40 early region from mutant tsA58. Expanding epithelial colonies were observed after 2 to 3 months, all of which grew to greater than 200 population doublings without crisis. All showed tight temperature dependence for growth. After switch-up to the restrictive temperature (40.5 degrees C), no further increase in cell number was seen after 1 to 2 days. However, DNA synthesis declined much more slowly; the dissociation from cell division led to marked polyploidy. Viability was maintained for up to 2 weeks. Introduction of an inducible mutant ras gene into ts thyroid cells led, as expected, to morphological transformation at the permissive temperature when ras was induced. Interestingly, this was associated with a marked reduction in net growth rate. At the restrictive temperature, induction of mutant ras caused rapid cell death. These results demonstrate the utility of a ts SV40 mutant to permit the study of oncogene action in an otherwise nonproliferative target cell and reveal important differences in the interaction between ras and SV40 T in these epithelial cells compared with previously studied cell types.



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