J 2019

p53 Binds Preferentially to Non-B DNA Structures Formed by the Pyrimidine-Rich Strands of GAA center dot TTC Trinucleotide Repeats Associated with Friedreich's Ataxia

HELMA, R., P. BAZANTOVA, M. PETR, M. ADAMIK, D. RENCIUK et. al.

Základní údaje

Originální název

p53 Binds Preferentially to Non-B DNA Structures Formed by the Pyrimidine-Rich Strands of GAA center dot TTC Trinucleotide Repeats Associated with Friedreich's Ataxia

Autoři

HELMA, R. (203 Česká republika), P. BAZANTOVA (203 Česká republika), M. PETR (203 Česká republika), M. ADAMIK (203 Česká republika), D. RENCIUK (203 Česká republika), V. TICHY (203 Česká republika), A. PASTUCHOVA (203 Česká republika), Z. SOLDANOVA (203 Česká republika), P. PECINKA (203 Česká republika), R.P. BOWATER (826 Velká Británie a Severní Irsko), Miroslav FOJTA (203 Česká republika, garant, domácí) a M. BRAZDOVA (203 Česká republika)

Vydání

Molecules, BASEL, Mayer und Muller, 2019, 1420-3049

Další údaje

Jazyk

angličtina

Typ výsledku

Článek v odborném periodiku

Obor

10608 Biochemistry and molecular biology

Stát vydavatele

Švýcarsko

Utajení

není předmětem státního či obchodního tajemství

Odkazy

Impakt faktor

Impact factor: 3.267

Kód RIV

RIV/00216224:14740/19:00110732

Organizační jednotka

Středoevropský technologický institut

UT WoS

000472631000051

Klíčová slova anglicky

trinucleotide repeat; p53; non-B DNA; DNA hairpin; DNA-protein; frataxin

Štítky

Příznaky

Mezinárodní význam, Recenzováno
Změněno: 13. 2. 2020 13:23, Mgr. Pavla Foltynová, Ph.D.

Anotace

V originále

Expansions of trinucleotide repeats (TNRs) are associated with genetic disorders such as Friedreich's ataxia. The tumor suppressor p53 is a central regulator of cell fate in response to different types of insults. Sequence and structure-selective modes of DNA recognition are among the main attributes of p53 protein. The focus of this work was analysis of the p53 structure-selective recognition of TNRs associated with human neurodegenerative diseases. Here, we studied binding of full length p53 and several deletion variants to TNRs folded into DNA hairpins or loops. We demonstrate that p53 binds to all studied non-B DNA structures, with a preference for non-B DNA structures formed by pyrimidine (Py) rich strands. Using deletion mutants, we determined the C-terminal DNA binding domain of p53 to be crucial for recognition of such non-B DNA structures. We also observed that p53 in vitro prefers binding to the Py-rich strand over the purine (Pu) rich strand in non-B DNA substrates formed by sequence derived from the first intron of the frataxin gene. The binding of p53 to this region was confirmed using chromatin immunoprecipitation in human Friedreich's ataxia fibroblast and adenocarcinoma cells. Altogether these observations provide further evidence that p53 binds to TNRs' non-B DNA structures.

Návaznosti

692068, interní kód MU
Název: BISON - Bridging Structural Biology with Biological Synthesis and Self Assembly to Reveal Key Processes in Living Systems (Akronym: BISON)
Investor: Evropská unie, BISON - Bridging Structural Biology with Biological Synthesis and Self Assembly to Reveal Key Processes in Living Systems, Spreading excellence and widening participation