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
—