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PMID: 8099841 Published · ppublish English Comparative Study Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Gain of function mutations in p53.

Nature genetics ·Vol. 4 ·No. 1 ·1993-05-00 ·Pages 42-6

Dittmer D, Pati S, Zambetti G, Chu S, Teresky AK, Moore M, Finlay C, Levine AJ

Abstract

We report that the expression of murine or human mutant p53 proteins in cells with no endogenous p53 proteins confers new or additional phenotypes upon these cells. Mutant p53 proteins expressed in cell lines lacking p53 resulted in either enhanced tumorigenic potential in nude mice ((10)3 cells) or enhanced plating efficiency in agar cell culture (human SAOS-2 cells). Also, mutant human p53 alleles, unlike the wild-type p53 protein, could also enhance the expression of a test gene regulated by the multi-drug resistance enhancer-promoter element. These data demonstrate a gain of function associated with p53 mutations in addition to the loss of function shown previously to be associated with mutations in this tumour suppressor gene.

MeSH Terms
ATP Binding Cassette Transporter, Subfamily B, Member 1 Animals Carrier Proteins/biosynthesis,genetics Cell Division/genetics Cell Line Clone Cells/transplantation Gene Expression Regulation/genetics Genes, p53 Humans Membrane Glycoproteins/biosynthesis,genetics Mice Mice, Inbred BALB C Mice, Nude Mutation Neoplasms, Experimental/genetics Phenotype Species Specificity Tumor Cells, Cultured Tumor Suppressor Protein p53/deficiency,genetics,physiology
Chemicals
ATP Binding Cassette Transporter, Subfamily B, Member 1 Carrier Proteins Membrane Glycoproteins Tumor Suppressor Protein p53
Authors & Affiliations
8 authors, click to expand affiliations / ORCID
Dittmer D
Department of Molecular Biology, Princeton University, New Jersey 08544-1014.
Pati S
Zambetti G
Chu S
Teresky A K
Moore M
Finlay C
Levine A J
Article Info
Journal
Nature genetics
Abbr.
Nat Genet
ISSN
1061-4036
Published
1993-05-00
Pages
42-6
Language
English
Region
United States
NLM ID
9216904
Subset
IM
Grants
NCI NIH HHS · P01 CA 41086 · United States
NCI NIH HHS · R01 CA55036 · United States
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