Interrupting the Early Region of Polyoma Virus DNA Enhances Tumorigenicity

The tumorigenicity of DNA from polyoma virus after cleavage with a variety of restriction enzymes was evaluated in suckling hamsters. Cleavage with enzymes that interrupt the region of the genome coding for the large tumor (T) antigen of polyoma virus markedly enhanced the tumorigenicity above that...

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Veröffentlicht in:Proceedings of the National Academy of Sciences - PNAS 1979-08, Vol.76 (8), p.3713-3716
Hauptverfasser: Israel, Mark A., Simmons, Daniel T., Hourihan, Sara L., Rowe, Wallace P., Martin, Malcolm A.
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container_issue 8
container_start_page 3713
container_title Proceedings of the National Academy of Sciences - PNAS
container_volume 76
creator Israel, Mark A.
Simmons, Daniel T.
Hourihan, Sara L.
Rowe, Wallace P.
Martin, Malcolm A.
description The tumorigenicity of DNA from polyoma virus after cleavage with a variety of restriction enzymes was evaluated in suckling hamsters. Cleavage with enzymes that interrupt the region of the genome coding for the large tumor (T) antigen of polyoma virus markedly enhanced the tumorigenicity above that observed with DNA I of the virus. Cell lines established in vitro from tumors induced by polyoma virions, polyoma virus DNA I, or polyoma virus DNA that had been cleaved with restriction endonucleases in the early region all contain the polyoma virus middle and small T antigens but not the large T antigen. These findings indicate that the large T antigen of polyoma virus is not required for maintenance of the transformed state and probably not for initiation of tumorigenesis by viral DNA.
doi_str_mv 10.1073/pnas.76.8.3713
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Cleavage with enzymes that interrupt the region of the genome coding for the large tumor (T) antigen of polyoma virus markedly enhanced the tumorigenicity above that observed with DNA I of the virus. Cell lines established in vitro from tumors induced by polyoma virions, polyoma virus DNA I, or polyoma virus DNA that had been cleaved with restriction endonucleases in the early region all contain the polyoma virus middle and small T antigens but not the large T antigen. 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Cleavage with enzymes that interrupt the region of the genome coding for the large tumor (T) antigen of polyoma virus markedly enhanced the tumorigenicity above that observed with DNA I of the virus. Cell lines established in vitro from tumors induced by polyoma virions, polyoma virus DNA I, or polyoma virus DNA that had been cleaved with restriction endonucleases in the early region all contain the polyoma virus middle and small T antigens but not the large T antigen. These findings indicate that the large T antigen of polyoma virus is not required for maintenance of the transformed state and probably not for initiation of tumorigenesis by viral DNA.</abstract><cop>United States</cop><pub>National Academy of Sciences of the United States of America</pub><pmid>226975</pmid><doi>10.1073/pnas.76.8.3713</doi><tpages>4</tpages><oa>free_for_read</oa></addata></record>
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subjects Animals
Antigens, Neoplasm - genetics
Base Sequence
Cell lines
Cell Transformation, Viral
Cricetinae
DNA
DNA, Viral - genetics
Enzymes
Genes, Viral
Hamsters
Molecular Weight
Neoplasms, Experimental - microbiology
Polyomavirus
Polyomavirus - genetics
Polyomavirus - pathogenicity
Transformed cell line
Tumor cell line
Tumors
Viral DNA
Viral genomes
Viral Proteins - genetics
title Interrupting the Early Region of Polyoma Virus DNA Enhances Tumorigenicity
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