Abstract
Cloned polyomavirus genomes encoding the small T antigen or truncated forms of the middle T antigen facilitated the growth of genomes encoding only the large T antigen in mouse 3T6 cells. We conclude that an N-terminal domain of the middle T antigen, in the appropriate cellular location, can substitute for the small T antigen during lytic infection.
MeSH Terms
Animals
Antigens, Polyomavirus Transforming
Antigens, Viral, Tumor/genetics,physiology
Cell Compartmentation
Cell Line
Cell Transformation, Viral
Cloning, Molecular
Cytopathogenic Effect, Viral
DNA, Viral/genetics
Mice
Oncogene Proteins, Viral/genetics,physiology
Peptide Fragments/genetics,physiology
Polyomavirus/genetics,physiology
Recombinant Proteins/physiology
Transfection
Chemicals
Antigens, Polyomavirus Transforming
Antigens, Viral, Tumor
DNA, Viral
Oncogene Proteins, Viral
Peptide Fragments
Recombinant Proteins
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Templeton D
Simon S
Eckhart W
References (11)
11 references, click to expand
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