Common features of polyomavirus mutants selected on PCC4 embryonal carcinoma cells.
AUTOR(ES)
Melin, F
RESUMO
The genomic rearrangements of six polyomavirus mutants selected on PCC4 embryonal carcinoma cells have been compared and their common characteristics pointed out. All mutants show a duplication which includes at least the adenovirus type 5 (Ad5) E1A-like enhancer core sequence plus a deletion of variable size and location. The presence of the second enhancer core sequence, the SV40-like enhancer, is not required for expression of the PyEC PCC4 phenotype. Two of these mutants are also able to express polyomavirus T antigen on F9 and LT1 cells. Multiadaptation seems to require the duplication of the Ad5 E1A-like core sequence, the maintenance of the SV40-like core sequence and a local change in DNA stability.
ACESSO AO ARTIGO
http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=554420Documentos Relacionados
- Isolation of polyomavirus mutants multiadapted to murine embryonal carcinoma cells.
- Analysis of transcription factors binding to the duplicated PEA1 and PEA3 sites that are required for polyomavirus mutant expression in PCC4 embryonic carcinoma cells.
- Negative regulation of early polyomavirus expression in mouse embryonal carcinoma cells.
- Retroviral mutants efficiently expressed in embryonal carcinoma cells.
- T-antigen-independent replication of polyomavirus DNA in murine embryonal carcinoma cells.