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Mouse Tcf3 represses canonical Wnt signaling by either competing for beta-catenin binding or through occupation of DNA-binding sites

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F68378050%3A_____%2F12%3A00387847" target="_blank" >RIV/68378050:_____/12:00387847 - isvavai.cz</a>

  • Result on the web

    <a href="http://dx.doi.org/10.1007/s11010-012-1243-9" target="_blank" >http://dx.doi.org/10.1007/s11010-012-1243-9</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1007/s11010-012-1243-9" target="_blank" >10.1007/s11010-012-1243-9</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Mouse Tcf3 represses canonical Wnt signaling by either competing for beta-catenin binding or through occupation of DNA-binding sites

  • Original language description

    Tcf3 acts as a transcription factor controlling gene expression in canonical Wnt signaling. In this study we show that mouse Tcf3 represses canonical Wnt signaling in mouse neural stem cells and in human HEK 293 cells. We demonstrate that mouse Tcf3 mediates repression of both moderate and high levels of canonical Wnt signaling, by either competing with other members of the Tcf/Lef family for binding to beta-catenin, or for binding to DNA. We observed that the repressor activity of mouse Tcf3 was only relieved effectively upon simultaneous disruption of both mechanisms. Immunofluorescence of transfected HEK 293 cells showed co-localization of beta-catenin and Tcf3 in the nucleus of cells transfected with full-length Tcf3, but not in cells transfected with N-terminal deleted versions. A direct physical interaction between beta-catenin and Tcf3 in the nucleus was confirmed by co-immunoprecipitation studies. The inhibitory beta-catenin/Tcf3 interface was independent of the ability of Tcf3

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)

  • CEP classification

    EB - Genetics and molecular biology

  • OECD FORD branch

Result continuities

  • Project

  • Continuities

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Others

  • Publication year

    2012

  • Confidentiality

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

Data specific for result type

  • Name of the periodical

    Molecular and Cellular Biochemistry

  • ISSN

    0300-8177

  • e-ISSN

  • Volume of the periodical

    365

  • Issue of the periodical within the volume

    1-2

  • Country of publishing house

    US - UNITED STATES

  • Number of pages

    11

  • Pages from-to

    53-63

  • UT code for WoS article

    000303472400007

  • EID of the result in the Scopus database