Literature DB >> 9433138

TCF/LEF factor earn their wings.

H Clevers1, M van de Wetering.   

Abstract

Factors of the TCF/LEF HMG domain family (TCFs) exist in vertebrates, Drosophila melanogaster and Caenorhabditis elegans. It has very recently become evident that TCFs interact with the vertebrate WNT effector beta-catenin to mediate axis formation in Xenopus. Likewise, Armadillo (the Drosophila ortholog of beta-catenin) is genetically upstream of a Drosophila TCF in the Wingless pathway. Upon Wingless/Wnt signaling, Armadillo/beta-catenin associate with nuclear TCFs and contribute a trans-activation domain to the resulting bipartite transcription factor. The cytoplasmic tumor-suppressor protein APC binds to beta-catenin causing its destruction. In APC-deficient colon carcinoma cells, beta-catenin accumulates and is constitutively complexed with TCF factors. In APC-positive colon carcinomas and melanomas, dominant mutations in beta-catenin render it indestructable, providing an alternative mechanism to activate transcription of TCF target genes inappropriately. So, transcriptional activation of TCF target genes by beta-catenin appears to be a central event in development and cellular transformation.

Entities:  

Mesh:

Substances:

Year:  1997        PMID: 9433138     DOI: 10.1016/s0168-9525(97)01305-x

Source DB:  PubMed          Journal:  Trends Genet        ISSN: 0168-9525            Impact factor:   11.639


  73 in total

Review 1.  Regulation of mammary gland development by tissue interaction.

Authors:  G W Robinson; A B Karpf; K Kratochwil
Journal:  J Mammary Gland Biol Neoplasia       Date:  1999-01       Impact factor: 2.673

2.  The SKN-1 amino-terminal arm is a DNA specificity segment.

Authors:  T Kophengnavong; A S Carroll; T K Blackwell
Journal:  Mol Cell Biol       Date:  1999-04       Impact factor: 4.272

Review 3.  Acetylation of histones and transcription-related factors.

Authors:  D E Sterner; S L Berger
Journal:  Microbiol Mol Biol Rev       Date:  2000-06       Impact factor: 11.056

4.  An F-box protein, FWD1, mediates ubiquitin-dependent proteolysis of beta-catenin.

Authors:  M Kitagawa; S Hatakeyama; M Shirane; M Matsumoto; N Ishida; K Hattori; I Nakamichi; A Kikuchi; K Nakayama; K Nakayama
Journal:  EMBO J       Date:  1999-05-04       Impact factor: 11.598

5.  Wnt11 signaling promotes proliferation, transformation, and migration of IEC6 intestinal epithelial cells.

Authors:  Lillian Ouko; Thomas R Ziegler; Li H Gu; Leonard M Eisenberg; Vincent W Yang
Journal:  J Biol Chem       Date:  2004-04-14       Impact factor: 5.157

Review 6.  A Comprehensive Overview of Skeletal Phenotypes Associated with Alterations in Wnt/β-catenin Signaling in Humans and Mice.

Authors:  Kevin A Maupin; Casey J Droscha; Bart O Williams
Journal:  Bone Res       Date:  2013-03-29       Impact factor: 13.567

7.  HIC1 attenuates Wnt signaling by recruitment of TCF-4 and beta-catenin to the nuclear bodies.

Authors:  Tomas Valenta; Jan Lukas; Lenka Doubravska; Bohumil Fafilek; Vladimir Korinek
Journal:  EMBO J       Date:  2006-05-25       Impact factor: 11.598

8.  Common genetic variation in sFRP5 is associated with fat distribution in men.

Authors:  J K Van Camp; S Beckers; D Zegers; A Verrijken; L F Van Gaal; W Van Hul
Journal:  Endocrine       Date:  2013-11-28       Impact factor: 3.633

Review 9.  Immunobiology of hepatocarcinogenesis: Ways to go or almost there?

Authors:  Pavan Patel; Steven E Schutzer; Nikolaos Pyrsopoulos
Journal:  World J Gastrointest Pathophysiol       Date:  2016-08-15

10.  Integration of cellular adhesion and Wnt signaling: Interactions between N-cadherin and LRP5 and their role in regulating bone mass.

Authors:  Zhendong Zhong; Bart O Williams
Journal:  J Bone Miner Res       Date:  2012-09       Impact factor: 6.741

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.