NAVRATILOVA, L., Marie BRAZDOVA, V. TICHY, Miroslav FOJTA, Matej LEXA, I. KYJOVSKY, W. DEPPERT and E. PALEČEK. Recognition of non-canonical DNA structures in genomic DNA sequences by p53 proteins. In 34th Congress of the Federation-of-European-Biochemical-Societies Prague. 2009. ISSN 1742-464X.
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Basic information
Original name Recognition of non-canonical DNA structures in genomic DNA sequences by p53 proteins
Name in Czech Ropoznávání nekanonických DNA struktur v genomových sekvencích DNA proteiny p53
Authors NAVRATILOVA, L. (203 Czech Republic), Marie BRAZDOVA (203 Czech Republic), V. TICHY (203 Czech Republic), Miroslav FOJTA (203 Czech Republic), Matej LEXA (703 Slovakia, belonging to the institution), I. KYJOVSKY (203 Czech Republic), W. DEPPERT (276 Germany) and E. PALEČEK (203 Czech Republic, guarantor).
Edition 34th Congress of the Federation-of-European-Biochemical-Societies Prague, 2009.
Other information
Original language English
Type of outcome Conference abstract
Field of Study Genetics and molecular biology
Country of publisher United States of America
Confidentiality degree is not subject to a state or trade secret
Impact factor Impact factor: 3.042
RIV identification code RIV/00216224:14330/09:00048866
Organization unit Faculty of Informatics
ISSN 1742-464X
UT WoS 000267069900306
Keywords in English p53; triplex DNA; DNA-binding; gene regulation
Changed by Changed by: doc. Ing. Matej Lexa, Ph.D., učo 31298. Changed: 23/9/2013 21:49.
Abstract
In our analyses we combined molecular and computational approaches to understand the mutant p53 function in specific gene regulation via binding to non-canonical DNA structures in chromatin DNA. We used two glioblastoma cell lines U251 (R273H) and Onda11 (R273C) expressing endogenous mutp53 proteins to isolate natural mutant p53 binding sites (mutp53BS) by genome- wide ChIP-cloning. In our computational work, we developed tools for rapid identification of DNA sequences (among the isolated mutp53BS) tending to form non-B structures (hairpins and triplex DNA) as well as for mapping their genomic locations. These sites are frequently localized in the regulatory first introns of genes and are enriched in repetitive elements. Potential to form triplex and cruciform structures was predicted by developed computational tools and detected by enzymatic and chemical probing. The role of topological status of studied DNA and p53 domains in mutp53BS recognition was investigated by recombinant mutp53 proteins in vitro and reporter assays in vivo. Our data suggest that the mutant p53 proteins bind selectively non-B DNA structures not only in vitro but also with functional consequences in vivo.
Links
GA204/08/1560, research and development projectName: Bioinformatická a experimentální identifikace nekanonických struktur v genomové DNA
Investor: Czech Science Foundation, In vitro and in silico identification of non-canonical DNA structures in genomic sequences
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