| Literature DB >> 9364015 |
A Inga1, S Cresta, P Monti, A Aprile, G Scott, A Abbondandolo, R Iggo, G Fronza.
Abstract
Analysis of families with germline p53 mutations shows that the mutant p53 allele behaves as a dominant oncogene at the genetic level, although it behaves as a recessive oncogene at the cellular level, since tumours invariably show mutation or loss of both wild-type alleles. At the biochemical level it is possible that some clinically important mutant p53 proteins may be carcinogenic through a dominant mechanism. We show that p53 mutants can be readily classified according to their dominant potential using a simple yeast functional assay. Wild-type p53 is constitutively expressed from a TRP1 vector, p53 mutants are expressed from an otherwise identical LEU2 vector and net transcriptional activity is scored using an ADE2-based reporter. Twenty seven p53 mutants were tested: 19 were recessive, i.e. gave white colonies, and eight showed dominant activity, i.e. gave pink/red colonies. This simple assay should facilitate studies on p53 dominance.Entities:
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Year: 1997 PMID: 9364015 DOI: 10.1093/carcin/18.10.2019
Source DB: PubMed Journal: Carcinogenesis ISSN: 0143-3334 Impact factor: 4.944