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p53 Specifically Binds Triplex DNA In Vitro and in Cells
M. Brázdová, V. Tichý, R. Helma, P. Bažantová, A. Polášková, A. Krejčí, M. Petr, L. Navrátilová, O. Tichá, K. Nejedlý, ML. Bennink, V. Subramaniam, Z. Bábková, T. Martínek, M. Lexa, M. Adámik,
Jazyk angličtina Země Spojené státy americké
Typ dokumentu časopisecké články
NLK
Directory of Open Access Journals
od 2006
Free Medical Journals
od 2006
Public Library of Science (PLoS)
od 2006
PubMed Central
od 2006
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od 2006-12-01
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od 2006-01-01
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od 2006-01-01
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od 2006-10-01
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od 2008-01-01
Nursing & Allied Health Database (ProQuest)
od 2006-12-01
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od 2006-12-01
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od 2006-12-01
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- MeSH
- aktivace transkripce genetika MeSH
- DNA vazebné proteiny chemie genetika MeSH
- DNA chemie genetika MeSH
- konformace nukleové kyseliny MeSH
- lidé MeSH
- nádorový supresorový protein p53 chemie genetika MeSH
- nukleotidové motivy genetika MeSH
- plazmidy genetika MeSH
- promotorové oblasti (genetika) MeSH
- regulační oblasti nukleových kyselin genetika MeSH
- sekvenční delece genetika MeSH
- vazebná místa MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
Triplex DNA is implicated in a wide range of biological activities, including regulation of gene expression and genomic instability leading to cancer. The tumor suppressor p53 is a central regulator of cell fate in response to different type of insults. Sequence and structure specific modes of DNA recognition are core attributes of the p53 protein. The focus of this work is the structure-specific binding of p53 to DNA containing triplex-forming sequences in vitro and in cells and the effect on p53-driven transcription. This is the first DNA binding study of full-length p53 and its deletion variants to both intermolecular and intramolecular T.A.T triplexes. We demonstrate that the interaction of p53 with intermolecular T.A.T triplex is comparable to the recognition of CTG-hairpin non-B DNA structure. Using deletion mutants we determined the C-terminal DNA binding domain of p53 to be crucial for triplex recognition. Furthermore, strong p53 recognition of intramolecular T.A.T triplexes (H-DNA), stabilized by negative superhelicity in plasmid DNA, was detected by competition and immunoprecipitation experiments, and visualized by AFM. Moreover, chromatin immunoprecipitation revealed p53 binding T.A.T forming sequence in vivo. Enhanced reporter transactivation by p53 on insertion of triplex forming sequence into plasmid with p53 consensus sequence was observed by luciferase reporter assays. In-silico scan of human regulatory regions for the simultaneous presence of both consensus sequence and T.A.T motifs identified a set of candidate p53 target genes and p53-dependent activation of several of them (ABCG5, ENOX1, INSR, MCC, NFAT5) was confirmed by RT-qPCR. Our results show that T.A.T triplex comprises a new class of p53 binding sites targeted by p53 in a DNA structure-dependent mode in vitro and in cells. The contribution of p53 DNA structure-dependent binding to the regulation of transcription is discussed.
Department of Information Technologies Faculty of Informatics Masaryk University Brno Czech Republic
Citace poskytuje Crossref.org
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