Reacquisition of a functional early region by a mouse transformant containing only defective simian virus 40 DNA

Author:

Chen S,Blanck G,Pollack R

Abstract

Viral DNA in simian virus 40-transformed mouse cells is capable of rearranging with passage. In this report, we show that such rearrangement can include an alteration in viral protein expression. SVT2, a simian virus 40-transformed mouse BALB/c 3T3 cell line, synthesizes only a super T antigen of molecular weight 100,000 without synthesizing the lytic-size large T or small t antigens with molecular weights of 94,000 and 17,000, respectively. Analyses of the integrated viral DNA revealed an early region of 4.4 kilobases instead of the lytic-size 2.7 kilobases. However, upon subcloning in either plastic or agarose or after being in culture for several passages, the appearance of lytic-size large T and small t antigens was detected. Concurrently, an early region of 2.7 kilobases, in addition to one of 4.4 kilobases, was observed.

Publisher

American Society for Microbiology

Subject

Cell Biology,Molecular Biology

Reference17 articles.

1. Rearrangement of integrated viral DNA sequences in mouse cells transformed by simian virus 40;Bender M. A.;J. Virol.,1981

2. Integration, loss, and reacquisition of defective viral DNA in SV40-transformed mouse cell lines;Blanck G.;Virology,1983

3. Nonlytic simian virus 40-specific 100K phosphoprotein is associated with anchorage-independent growth in simian virus 40-transformed and revertant mouse cell lines;Chen S.;Mol. Cell. Biol.,1981

4. Cloning and characterization of the integrated viral DNA from three lines of SV40-transformed mouse cells;Clayton C.;Cell,1981

5. Functional analysis of a simian virus 40 super T-antigen;Clayton C. E.;J. Virol.,1982

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