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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

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    0520186 - BFÚ 2020 RIV CH eng J - Journal Article
    Helma, Robert - Bažantová, Pavla - Petr, Marek - Adámik, Matěj - Renčiuk, Daniel - Tichý, Vlastimil - Pastuchová, Alena - Soldanová, Zuzana - Pečinka, Petr - Bowater, R. P. - Fojta, Miroslav - Brázdová, Marie
    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.
    Molecules. Roč. 24, č. 11 (2019), č. článku 2078. E-ISSN 1420-3049
    R&D Projects: GA ČR(CZ) GA19-15168S; GA ČR(CZ) GA16-01625S; GA ČR(CZ) GJ17-19170Y; GA MŠMT EF15_003/0000477
    Institutional support: RVO:68081707
    Keywords : dynamic mutations * disease * length
    OECD category: Biochemistry and molecular biology
    Impact factor: 3.267, year: 2019
    Method of publishing: Open access
    https://www.mdpi.com/1420-3049/24/11/2078/pdf

    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.
    Permanent Link: http://hdl.handle.net/11104/0304872

     
     
Number of the records: 1  

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