2013
Preferential Binding of Hot Spot Mutant p53 Proteins to Supercoiled DNA In Vitro and in Cells
BRÁZDOVÁ, Marie, Lucie NAVRATILOVA, Vlastimil TICHÝ, Kateřina NĚMCOVÁ, Matej LEXA et. al.Základní údaje
Originální název
Preferential Binding of Hot Spot Mutant p53 Proteins to Supercoiled DNA In Vitro and in Cells
Autoři
BRÁZDOVÁ, Marie (203 Česká republika), Lucie NAVRATILOVA (203 Česká republika), Vlastimil TICHÝ (203 Česká republika, garant, domácí), Kateřina NĚMCOVÁ (203 Česká republika), Matej LEXA (703 Slovensko, domácí), Roman HRSTKA (203 Česká republika), Petr PECINKA (203 Česká republika), Matej ADÁMIK (703 Slovensko, domácí), Bořivoj VOJTĚŠEK (203 Česká republika), Emil PALECEK (203 Česká republika), Wolfgang DEPPERT (276 Německo) a Miroslav FOJTA (203 Česká republika, domácí)
Vydání
Plos One, SAN FRANCISCO, PUBLIC LIBRARY SCIENCE, 2013, 1932-6203
Další údaje
Jazyk
angličtina
Typ výsledku
Článek v odborném periodiku
Obor
10608 Biochemistry and molecular biology
Stát vydavatele
Spojené státy
Utajení
není předmětem státního či obchodního tajemství
Odkazy
Impakt faktor
Impact factor: 3.534
Kód RIV
RIV/00216224:14330/13:00066842
Organizační jednotka
Fakulta informatiky
UT WoS
000317418500055
Klíčová slova anglicky
p53 tumor supressor; mutp53 oncogenic mutations; DNA topology; superhelicity; DNA binding; BAX MSP/MST1 promoter
Změněno: 13. 3. 2018 14:20, doc. Ing. Matej Lexa, Ph.D.
Anotace
V originále
Hot spot mutant p53 (mutp53) proteins exert oncogenic gain-of-function activities. Binding of mutp53 to DNA is assumed to be involved in mutp53-mediated repression or activation of several mutp53 target genes. To investigate the importance of DNA topology on mutp53-DNA recognition in vitro and in cells, we analyzed the interaction of seven hot spot mutp53 proteins with topologically different DNA substrates (supercoiled, linear and relaxed) containing and/or lacking mutp53 binding sites (mutp53BS) using a variety of electrophoresis and immunoprecipitation based techniques. All seven hot spot mutp53 proteins (R175H, G245S, R248W, R249S, R273C, R273H and R282W) were found to have retained the ability of wild-type p53 to preferentially bind circular DNA at native negative superhelix density, while linear or relaxed circular DNA was a poor substrate. The preference of mutp53 proteins for supercoiled DNA (supercoil-selective binding) was further substantiated by competition experiments with linear DNA or relaxed DNA in vitro and ex vivo. Using chromatin immunoprecipitation, the preferential binding of mutp53 to a sc mutp53BS was detected also in cells. Furthermore, we have shown by luciferase reporter assay that the DNA topology influences p53 regulation of BAX and MSP/MST1 promoters. Possible modes of mutp53 binding to topologically constrained DNA substrates and their biological consequences are discussed.
Návaznosti
GA204/08/1560, projekt VaV |
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