BRÁZDOVÁ, Marie, Tomáš MARTÍNEK a Matej LEXA. In silico search for secondary structures in p53 target genes using R/Bioconductor. In Tomáš Vinař, Martin Holeňa, Matej Lexa, Ladislav Peška, Peter Vojtáš. ITAT 2013: Information Technologies - Applications and Theory (Workshops, Posters, and Tutorials). Neuvedeno: CreateSpace Independent Publishing Platform, 2013, s. 42-46. ISBN 1-4909-5208-X.
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Základní údaje
Originální název In silico search for secondary structures in p53 target genes using R/Bioconductor
Autoři BRÁZDOVÁ, Marie (203 Česká republika), Tomáš MARTÍNEK (203 Česká republika) a Matej LEXA (703 Slovensko, garant, domácí).
Vydání Neuvedeno, ITAT 2013: Information Technologies - Applications and Theory (Workshops, Posters, and Tutorials), od s. 42-46, 5 s. 2013.
Nakladatel CreateSpace Independent Publishing Platform
Další údaje
Originální jazyk angličtina
Typ výsledku Stať ve sborníku
Obor 10201 Computer sciences, information science, bioinformatics
Stát vydavatele Česká republika
Utajení není předmětem státního či obchodního tajemství
Forma vydání tištěná verze "print"
WWW URL
Kód RIV RIV/00216224:14330/13:00068953
Organizační jednotka Fakulta informatiky
ISBN 1-4909-5208-X
Klíčová slova česky R/bioconductor; p53; bioinformatics; DNA sequence analysis
Klíčová slova anglicky R/bioconductor; p53; bioinformatika; analýza sekvence DNA
Změnil Změnil: RNDr. Pavel Šmerk, Ph.D., učo 3880. Změněno: 28. 4. 2014 06:20.
Anotace
p53 is a well-known transcription factor and tumor suppressor, regulating among other processes, the commitment of cells to apoptosis and DNA repair. p53 mutants are often found in cancers of different kinds, ei- ther as mutant or misregulated p53. p53 is involved in many other processes and we currently do not understand the full range of its functions. It is known to recognize the p53con sequence by its specific DNA-binding domain (DBD). It is also known to bind DNA non-specifically. This binding has been shown to involve superhelical DNA, more specifically, cruciform, triplex and quadruplex struc- tures. In our laboratories we were intrigued by the possi- ble interplay between non-canonical DNA structure bind- ing and regular p53con binding. In an attempt to clarify this interplay and discover suitable candidate genes for fur- ther study, we carried out an in silico study on the human genome. We identified all the occurences of potential cru- ciform DNA, triplex DNA, quadruplex DNA and p53con recognition sequences in +/-40000 bp regions of known genes. We analyzed this data for statistically significant patterns and combinations of patterns using a small set of available R/Bioconductor packages. This paper describes the computational pipeline designed for this type of stud- ies. We also show preliminary results for selected human sequences.
Návaznosti
LG13010, projekt VaVNázev: Zastoupení ČR v European Research Consortium for Informatics and Mathematics (Akronym: ERCIM-CZ)
Investor: Ministerstvo školství, mládeže a tělovýchovy ČR, Zastoupení ČR v European Research Consortium for Informatics and Mathematics
VytisknoutZobrazeno: 26. 4. 2024 07:20