Literature DB >> 9118222

Armadillo coactivates transcription driven by the product of the Drosophila segment polarity gene dTCF.

M van de Wetering1, R Cavallo, D Dooijes, M van Beest, J van Es, J Loureiro, A Ypma, D Hursh, T Jones, A Bejsovec, M Peifer, M Mortin, H Clevers.   

Abstract

The vertebrate transcription factors TCF (T cell factor) and LEF (lymphocyte enhancer binding factor) interact with beta-catenin and are hypothesized to mediate Wingless/Wnt signaling. We have cloned a maternally expressed Drosophila TCF family member, dTCF. dTCF binds a canonical TCF DNA motif and interacts with the beta-catenin homolog Armadillo. Previous studies have identified two regions in Armadillo required for Wingless signaling. One of these interacts with dTCF, while the other constitutes a transactivation domain. Mutations in dTCF and expression of a dominant-negative dTCF transgene cause a segment polarity phenotype and affect expression of the Wingless target genes engrailed and Ultrabithorax. Epistasis analysis positions dTCF downstream of armadillo. The Armadillo-dTCF complex mediates Wingless signaling as a bipartite transcription factor.

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Year:  1997        PMID: 9118222     DOI: 10.1016/s0092-8674(00)81925-x

Source DB:  PubMed          Journal:  Cell        ISSN: 0092-8674            Impact factor:   41.582


  423 in total

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Authors:  M W Klymkowsky; B O Williams; G D Barish; H E Varmus; Y E Vourgourakis
Journal:  Mol Biol Cell       Date:  1999-10       Impact factor: 4.138

2.  Perturbation of the tight junction permeability barrier by occludin loop peptides activates beta-catenin/TCF/LEF-mediated transcription.

Authors:  I Vietor; T Bader; K Paiha; L A Huber
Journal:  EMBO Rep       Date:  2001-04       Impact factor: 8.807

3.  APC-mediated downregulation of beta-catenin activity involves nuclear sequestration and nuclear export.

Authors:  K L Neufeld; F Zhang; B R Cullen; R L White
Journal:  EMBO Rep       Date:  2000-12       Impact factor: 8.807

4.  HMG boxes of DSP1 protein interact with the rel homology domain of transcription factors.

Authors:  M Decoville; M J Giraud-Panis; C Mosrin-Huaman; M Leng; D Locker
Journal:  Nucleic Acids Res       Date:  2000-01-15       Impact factor: 16.971

5.  Direct regulation of nacre, a zebrafish MITF homolog required for pigment cell formation, by the Wnt pathway.

Authors:  R I Dorsky; D W Raible; R T Moon
Journal:  Genes Dev       Date:  2000-01-15       Impact factor: 11.361

6.  The p300/CBP acetyltransferases function as transcriptional coactivators of beta-catenin in vertebrates.

Authors:  A Hecht; K Vleminckx; M P Stemmler; F van Roy; R Kemler
Journal:  EMBO J       Date:  2000-04-17       Impact factor: 11.598

7.  Teashirt is required for transcriptional repression mediated by high Wingless levels.

Authors:  L Waltzer; L Vandel; M Bienz
Journal:  EMBO J       Date:  2001-01-15       Impact factor: 11.598

8.  Hemocytes are essential for wing maturation in Drosophila melanogaster.

Authors:  J A Kiger; J E Natzle; M M Green
Journal:  Proc Natl Acad Sci U S A       Date:  2001-08-14       Impact factor: 11.205

9.  The chromatin remodelling factor Brg-1 interacts with beta-catenin to promote target gene activation.

Authors:  N Barker; A Hurlstone; H Musisi; A Miles; M Bienz; H Clevers
Journal:  EMBO J       Date:  2001-09-03       Impact factor: 11.598

10.  PIASy, a nuclear matrix-associated SUMO E3 ligase, represses LEF1 activity by sequestration into nuclear bodies.

Authors:  S Sachdev; L Bruhn; H Sieber; A Pichler; F Melchior; R Grosschedl
Journal:  Genes Dev       Date:  2001-12-01       Impact factor: 11.361

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