Synthesis of virus-specific proteins in simian sarcoma virus-transformed primate cells

Virology ◽  
1981 ◽  
Vol 114 (1) ◽  
pp. 113-123 ◽  
Author(s):  
Carolyn M. Bergholz
Nature ◽  
1981 ◽  
Vol 294 (5838) ◽  
pp. 273-275 ◽  
Author(s):  
Flossie Wong-Staal ◽  
Riccardo Dalla Favera ◽  
Edward P. Gelmann ◽  
Vittorio Manzari ◽  
Stanislaw Szala ◽  
...  

1986 ◽  
Vol 6 (11) ◽  
pp. 3704-3710
Author(s):  
L Simonneau ◽  
P Crisanti ◽  
A M Lorinet ◽  
F Alliot ◽  
Y Courtois ◽  
...  

The lens-specific proteins alpha and delta crystallins and lentoid bodies, structures that follow a differentiation pathway similar to that of the lens, regularly appear after 4 to 5 weeks in quail embryo neuroretina monolayer cultures. We have investigated the effects of the avian oncogenic retroviruses Mill Hill 2 and Rous sarcoma virus on this process. Quail embryo neuroretina cells transformed by Mill Hill 2 virus were established into permanent cultures that synthesized alpha and delta crystallins and contained stem cells for the production of lentoid bodies. In contrast, transformation with the Rous sarcoma virus mutant tsNY-68 blocked the appearance of mRNA crystallins, but cytoplasmic alpha and delta crystallin mRNA and alpha crystallin appeared 44 h after a shift to the nonpermissive temperature. However, delta crystallins and lentoid bodies were only present after 7 days. The crystallins of transformed quail neuroretina cultures were immunologically indistinguishable from those of quail lenses and of normal quail embryo neuroretina cultures.


1977 ◽  
Vol 20 (1) ◽  
pp. 104-111 ◽  
Author(s):  
Carolyn M. Bergholz ◽  
Lauren G. Wolfe ◽  
Friedrich Deinhardt

Virology ◽  
1981 ◽  
Vol 114 (1) ◽  
pp. 124-131 ◽  
Author(s):  
H.-Jurgen Thiel ◽  
Thomas J. Matthews ◽  
Edward M. Broughton ◽  
Kent J. Weinhold ◽  
Dani P. Bolognesi ◽  
...  

1978 ◽  
Vol 33 (11-12) ◽  
pp. 969-980 ◽  
Author(s):  
F. Deinhardt ◽  
C. Bergholz ◽  
G. Hunsmann ◽  
J. Schneider ◽  
H.-J. Thiel ◽  
...  

The structural proteins of simian sarcoma virus type 1 and its associated virus (SSV) were analysed; in general they were similar to the corresponding components of murine leukemia viruses (MuLV), i. e. glycoproteins of approximately 69.000 and 71.000 Daltons (gp69/71), pro­teins corresponding to p15(E) and p12(E) which were identified as envelope, and p31, p15, p12 and p10 proteins identified as internal components. As in MuLV, p12 stained reddish with Coomassie blue but a pl5(C) distinct from p15(E) was not clearly identified. Using antisera specific for individual components of MuLV cross-reactions were observed between the proteins pl5(E), pi2(E) and p31 of SSV and MuLV, and to a minor degree also between their respective major glycoproteins. An antiserum reacting strongly, specifically and almost exclusively with the envelope components of SSV gp69/71, p15 (E) and p12 (E) was prepared in a goat by inoculation of the animal’s own cells, previously transformed in vitro with SSV and grown in goat serum. Comparative studies with this antiserum in complement fixation and Ouchterlony tests confirmed the strong antigenic similarities between SSV and gibbon ape lymphoma virus but did not identify any interspecies reactivity.


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