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Interaction of C-terminal p53 isoforms depends strongly upon DNA sequence and topology

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F68081707%3A_____%2F23%3A00574514" target="_blank" >RIV/68081707:_____/23:00574514 - isvavai.cz</a>

  • Alternative codes found

    RIV/62156489:43110/23:43922658 RIV/00216305:26210/22:PU146617

  • Result on the web

    <a href="https://www.sciencedirect.com/science/article/pii/S0300908422003352?via%3Dihub" target="_blank" >https://www.sciencedirect.com/science/article/pii/S0300908422003352?via%3Dihub</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1016/j.biochi.2022.12.011" target="_blank" >10.1016/j.biochi.2022.12.011</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Interaction of C-terminal p53 isoforms depends strongly upon DNA sequence and topology

  • Original language description

    The p53 protein is a key tumor suppressor and the most commonly mutated and down-regulated protein in human tumors. It functions mainly through interaction with DNA, and p53 acts as a transcription factor that recognizes the so-called p53 target sites on the promoters of various genes. P53 has been shown to exist as many isoforms, including three C-terminal isoforms that are produced by alternative splicing. Because the C-terminal domain is responsible for sequence-nonspecific binding and regulation of p53 binding, we have analyzed DNA recognition by these C-terminal isoforms. Using atomic force microscopy, we show for the first time that all C-terminal isoforms recognize superhelical DNA. It is particularly noteworthy that a sequence-specific p53 consensus binding site is bound by p53a and b isoforms with similar affinities, whilst p53a shows higher binding to a quadruplex sequence than both p53b and p53g, and p53g loses preferential binding to both the consensus binding sequence and the quadruplex-forming sequence. These results show the important role of the variable p53 C-terminal amino acid sequences for DNA recognition. (c) 2022 Elsevier B.V. and Societe Francaise de Biochimie et Biologie Moleculaire (SFBBM). All rights reserved.

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database

  • CEP classification

  • OECD FORD branch

    10608 - Biochemistry and molecular biology

Result continuities

  • Project

    <a href="/en/project/GA22-21903S" target="_blank" >GA22-21903S: Local DNA structures and their role in mutant p53 protein function in human tumours</a><br>

  • Continuities

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Others

  • Publication year

    2023

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    Biochimie

  • ISSN

    0300-9084

  • e-ISSN

    1638-6183

  • Volume of the periodical

    208

  • Issue of the periodical within the volume

    MAY 2023

  • Country of publishing house

    NL - THE KINGDOM OF THE NETHERLANDS

  • Number of pages

    7

  • Pages from-to

    93-99

  • UT code for WoS article

    001009864200001

  • EID of the result in the Scopus database

    2-s2.0-85144931283