Preferential binding of p53 tumor suppressor to p21 promoter sites that contain inverted repeats capable of forming cruciform structure
Language English Country United States Media print-electronic
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
24134839
DOI
10.1016/j.bbrc.2013.10.015
PII: S0006-291X(13)01675-6
Knihovny.cz E-resources
- Keywords
- Cruciform, Protein–DNA binding, p53,
- MeSH
- Chromatin Immunoprecipitation MeSH
- Fluorouracil pharmacology MeSH
- Cyclin-Dependent Kinase Inhibitor p21 genetics MeSH
- DNA, Cruciform genetics MeSH
- Humans MeSH
- Mutagens toxicity MeSH
- Cell Line, Tumor MeSH
- Tumor Suppressor Protein p53 metabolism MeSH
- Inverted Repeat Sequences genetics MeSH
- Computer Simulation MeSH
- Promoter Regions, Genetic * MeSH
- Response Elements genetics MeSH
- Base Sequence MeSH
- Protein Binding drug effects genetics MeSH
- Blotting, Western MeSH
- Check Tag
- Humans MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- Fluorouracil MeSH
- Cyclin-Dependent Kinase Inhibitor p21 MeSH
- DNA, Cruciform MeSH
- Mutagens MeSH
- Tumor Suppressor Protein p53 MeSH
p53 Is one of the most critical proteins involved in protecting organisms from malignancies and its gene is frequently mutated in these diseases. p53 Functions as a transcription factor and its role in the cell is mediated by sequence-specific DNA binding. Although the genome contains many p53-binding sequences, the p53 protein binds only a subset of these sequences with high affinity. One likely mechanism of how p53 binds DNA effectively underlies its ability to recognize selective local DNA structure. We analyzed the possibility of cruciform structure formation within different regions of the p21 gene promoter. p53 protein remarkably activates the transcription of p21 gene after genotoxic treatment. In silico analysis showed that p21 gene promoter contains numerous p53 target sequences, some of which have inverted repeats capable of forming cruciform structures. Using chromatin immunoprecipitation, we demonstrated that p53 protein binds preferentially to sequences that not only contain inverted repeats but also have the ability to create local cruciform structures. Gel retardation assay also revealed strong preference of the p53 protein for response element in superhelical state, with cruciform structure in the DNA sequence. Taken together, our results suggest that p53 response element's potential for cruciform structure formation could be an additional determinant in p53 DNA-binding machinery.
References provided by Crossref.org
Interaction of Proteins with Inverted Repeats and Cruciform Structures in Nucleic Acids
Characterization of p53 Family Homologs in Evolutionary Remote Branches of Holozoa
The Rich World of p53 DNA Binding Targets: The Role of DNA Structure
Recognition of Local DNA Structures by p53 Protein
Strong preference of BRCA1 protein to topologically constrained non-B DNA structures
DNA and RNA quadruplex-binding proteins