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PMID: 1301998 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Definition of a consensus binding site for p53.

Nature genetics ·Vol. 1 ·No. 1 ·1992-04-00 ·Pages 45-9

el-Deiry WS, Kern SE, Pietenpol JA, Kinzler KW, Vogelstein B

Abstract

Recent experiments have suggested that p53 action may be mediated through its interaction with DNA. We have now identified 18 human genomic clones that bind to p53 in vitro. Precise mapping of the binding sequences within these clones revealed a consensus binding site with a striking internal symmetry, consisting of two copies of the 10 base pair motif 5'-PuPuPuC(A/T)(T/A)GPyPyPy-3' separated by 0-13 base pairs. One copy of the motif was insufficient for binding, and subtle alterations of the motif, even when present in multiple copies, resulted in loss of affinity for p53. Mutants of p53, representing each of the four "hot spots" frequently altered in human cancers, failed to bind to the consensus dimer. These results define the DNA sequence elements with which p53 interacts in vitro and which may be important for p53 action in vivo.

MeSH Terms
Base Sequence Binding Sites Cloning, Molecular Consensus Sequence DNA/genetics,metabolism Humans Molecular Sequence Data Mutation Polymerase Chain Reaction Protein Binding Tumor Suppressor Protein p53/genetics,metabolism
Chemicals
Tumor Suppressor Protein p53 DNA
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
el-Deiry W S
Oncology Center, Johns Hopkins University School of Medicine, Baltimore, Maryland 21231.
Kern S E
Pietenpol J A
Kinzler K W
Vogelstein B
Article Info
Journal
Nature genetics
Abbr.
Nat Genet
ISSN
1061-4036
Published
1992-04-00
Pages
45-9
Language
English
Region
United States
NLM ID
9216904
Subset
IM
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