| pubmed-article:3309672 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:3309672 | lifeskim:mentions | umls-concept:C0012888 | lld:lifeskim |
| pubmed-article:3309672 | lifeskim:mentions | umls-concept:C0079419 | lld:lifeskim |
| pubmed-article:3309672 | lifeskim:mentions | umls-concept:C1167622 | lld:lifeskim |
| pubmed-article:3309672 | lifeskim:mentions | umls-concept:C0038973 | lld:lifeskim |
| pubmed-article:3309672 | lifeskim:mentions | umls-concept:C0719453 | lld:lifeskim |
| pubmed-article:3309672 | pubmed:issue | 6138 | lld:pubmed |
| pubmed-article:3309672 | pubmed:dateCreated | 1987-11-3 | lld:pubmed |
| pubmed-article:3309672 | pubmed:abstractText | The large T antigen (T) of simian virus 40 is a multifunctional protein required for both viral DNA replication and cellular transformation. T antigen forms specific protein complexes with the host protein p53 in both virus-infected and transformed cells. p53 has recently been shown to be an oncogene, but its normal function is not clear. We previously established a radioimmunoassay to study the newly described complex between T antigen and DNA polymerase alpha, and have noted a similarity between the antigenic changes induced in T by the binding of both p53 and polymerase. We now extend this analysis to a larger collection of anti-T antibodies and formally establish that p53 and DNA polymerase alpha can compete for binding to the SV40 T antigen. At a critical concentration of the three components it is possible to detect a trimeric complex of T, p53 and DNA polymerase alpha. Our observations have important implications for the control by these nuclear oncogenes of viral and cellular DNA synthesis and viral host range in both normal and transformed cells. We present a model for the action of p53 in growth control. | lld:pubmed |
| pubmed-article:3309672 | pubmed:language | eng | lld:pubmed |
| pubmed-article:3309672 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:3309672 | pubmed:citationSubset | IM | lld:pubmed |
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| pubmed-article:3309672 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:3309672 | pubmed:issn | 0028-0836 | lld:pubmed |
| pubmed-article:3309672 | pubmed:author | pubmed-author:LangD RDR | lld:pubmed |
| pubmed-article:3309672 | pubmed:author | pubmed-author:GannonJ VJV | lld:pubmed |
| pubmed-article:3309672 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:3309672 | pubmed:volume | 329 | lld:pubmed |
| pubmed-article:3309672 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:3309672 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:3309672 | pubmed:pagination | 456-8 | lld:pubmed |
| pubmed-article:3309672 | pubmed:dateRevised | 2005-11-17 | lld:pubmed |
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| pubmed-article:3309672 | pubmed:articleTitle | p53 and DNA polymerase alpha compete for binding to SV40 T antigen. | lld:pubmed |
| pubmed-article:3309672 | pubmed:affiliation | Imperial Cancer Research Fund, Clare Hall Laboratories, Herts, UK. | lld:pubmed |
| pubmed-article:3309672 | pubmed:publicationType | Journal Article | lld:pubmed |
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