BRÁZDOVÁ, Marie, Vlastimil TICHÝ, Robert HELMA, Pavla BAŽANTOVÁ, Alena POLÁŠKOVÁ, Aneta KREJČÍ, Marek PETR, Lucie NAVRÁTILOVÁ, Olga TICHÁ, Karel NEJEDLÝ, Martin L BENNINK, Vinod SUBRAMANIAM, Zuzana BÁBKOVÁ, Tomáš MARTÍNEK, Matej LEXA and Matej ADÁMIK. p53 Specifically Binds Triplex DNA In Vitro and in Cells. Online. PLOS ONE. Public Library of Science, 2016, vol. 11, No 12, p. "e0167439", 25 pp. ISSN 1932-6203. Available from: https://dx.doi.org/10.1371/journal.pone.0167439. [citováno 2024-04-24]
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Basic information
Original name p53 Specifically Binds Triplex DNA In Vitro and in Cells
Authors BRÁZDOVÁ, Marie (203 Czech Republic, guarantor), Vlastimil TICHÝ (203 Czech Republic), Robert HELMA (203 Czech Republic), Pavla BAŽANTOVÁ (203 Czech Republic), Alena POLÁŠKOVÁ (203 Czech Republic), Aneta KREJČÍ (203 Czech Republic), Marek PETR (203 Czech Republic), Lucie NAVRÁTILOVÁ (203 Czech Republic), Olga TICHÁ (203 Czech Republic), Karel NEJEDLÝ (203 Czech Republic), Martin L BENNINK (528 Netherlands), Vinod SUBRAMANIAM (528 Netherlands), Zuzana BÁBKOVÁ (203 Czech Republic), Tomáš MARTÍNEK (203 Czech Republic), Matej LEXA (703 Slovakia, belonging to the institution) and Matej ADÁMIK (703 Slovakia)
Edition PLOS ONE, Public Library of Science, 2016, 1932-6203.
Other information
Original language English
Type of outcome Article in a journal
Field of Study 10608 Biochemistry and molecular biology
Country of publisher United States of America
Confidentiality degree is not subject to a state or trade secret
WWW URL URL
Impact factor Impact factor: 2.806
RIV identification code RIV/00216224:14330/16:00088595
Organization unit Faculty of Informatics
Doi http://dx.doi.org/10.1371/journal.pone.0167439
UT WoS 000389482700156
Keywords in English cancer; H-DNA; non-B DNA; gene regulation; DNA binding;
Tags International impact, Reviewed
Changed by Changed by: Mgr. Martina Zapletalová, Ph.D., učo 357594. Changed: 20/1/2021 12:05.
Abstract
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.
Links
GA15-02891S, research and development projectName: Rostlinné transpozony a konformace DNA
Investor: Czech Science Foundation
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