Cellular immortalization by a cDNA clone encoding the transformation-associated phosphoprotein p53 View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

1984-12

AUTHORS

J R Jenkins, K Rudge, G A Currie

ABSTRACT

Malignant transformation of primary cells requires at least two distinct and characteristic alterations in cellular behaviour. The first, cellular immortality, can be induced by chemical carcinogens or by cloned oncogenes such as polyoma large T (ref. 4), adenovirus early region 1A (E1A) or the oncogene from avian (MC29) myelocytomatosis virus, v-myc. Cells whose in vitro life-span has been extended by these procedures can be fully transformed by transfection with oncogenes belonging to a different complementation group, including genes of the ras family, adenovirus E1b and polyoma virus middle T (refs 4, 5). The unstable cellular phosphoprotein p53 is frequently present at elevated levels in transformed cells and is stabilized by the formation of complexes with simian virus 40 (SV40) large T or adenovirus E1b 57K protein. Although several reports have associated p53 with cell proliferation, its role remains obscure. We have cloned complementary DNA sequences encoding murine p53 and report here that transfection of p53 expression constructs into cells of finite lifespan in vitro results in cellular immortality and susceptibility to transformation by a ras oncogene. More... »

PAGES

651-654

Identifiers

URI

http://scigraph.springernature.com/pub.10.1038/312651a0

DOI

http://dx.doi.org/10.1038/312651a0

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1047086040

PUBMED

https://www.ncbi.nlm.nih.gov/pubmed/6095117


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