A direct beta-catenin-independent interaction between androgen receptor and T cell factor 4 (Q24304373)

transcription factor 7 like 2

1 reference

catenin beta 1

1 reference

negative regulation of transcription, DNA-templated

1 reference

Moumita Barua

2

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author name string

Avital L Amir

1

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Nicole C McKnight

3

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Shinta Cheng

4

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Xin Yuan

5

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Steven P Balk

Journal of Biological Chemistry

6

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publication date

15 August 2003

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language of work or name

English

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published in

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volume

278

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issue

33

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page(s)

30828-34

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cites work

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FXXLF and WXXLF sequences mediate the NH2-terminal interaction with the ligand binding domain of the androgen receptor

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The DNA-bending protein HMG-1 enhances progesterone receptor binding to its target DNA sequences

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The High Mobility Group Protein 1 Enhances Binding of the Estrogen Receptor DNA Binding Domain to the Estrogen Response Element

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High-Mobility Group Chromatin Proteins 1 and 2 Functionally Interact with Steroid Hormone Receptors To Enhance Their DNA Binding In Vitro and Transcriptional Activity in Mammalian Cells

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HMG-1 stimulates estrogen response element binding by estrogen receptor from stably transfected HeLa cells

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SRY interacts with and negatively regulates androgen receptor transcriptional activity

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Depletion of epithelial stem-cell compartments in the small intestine of mice lacking Tcf-4

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Restricted high level expression of Tcf-4 protein in intestinal and mammary gland epithelium

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All Tcf HMG box transcription factors interact with Groucho-related co-repressors

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In vitro evidence for complex modes of nuclear beta-catenin signaling during prostate growth and tumorigenesis

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T-cell factors: turn-ons and turn-offs

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The HMG domain of lymphoid enhancer factor 1 bends DNA and facilitates assembly of functional nucleoprotein structures

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Functional interaction of beta-catenin with the transcription factor LEF-1

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XTcf-3 transcription factor mediates beta-catenin-induced axis formation in Xenopus embryos

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Nuclear localization of beta-catenin by interaction with transcription factor LEF-1

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Constitutive transcriptional activation by a beta-catenin-Tcf complex in APC-/- colon carcinoma

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Activation of beta-catenin-Tcf signaling in colon cancer by mutations in beta-catenin or APC

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

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pangolin encodes a Lef-1 homologue that acts downstream of Armadillo to transduce the Wingless signal in Drosophila.

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Human homologs of a Drosophila Enhancer of split gene product define a novel family of nuclear proteins

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The Xenopus Wnt effector XTcf-3 interacts with Groucho-related transcriptional repressors

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Drosophila Tcf and Groucho interact to repress Wingless signalling activity

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Transcriptional repression by AML1 and LEF-1 is mediated by the TLE/Groucho corepressors

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Binding of GSK3beta to the APC-beta-catenin complex and regulation of complex assembly

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Crystal structure of a beta-catenin/Tcf complex

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Structure of a human Tcf4-beta-catenin complex

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Mapping DNA interaction sites of chromosomal proteins using immunoprecipitation and polymerase chain reaction

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

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Regulation of Lef-mediated transcription and p53-dependent pathway by associating beta-catenin with CBP/p300.

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The transcriptional coactivator CBP interacts with beta-catenin to activate gene expression

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

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Synergistic coactivator function by coactivator-associated arginine methyltransferase (CARM) 1 and beta-catenin with two different classes of DNA-binding transcriptional activators

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Linking beta-catenin to androgen-signaling pathway

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The androgen receptor can promote beta-catenin nuclear translocation independently of adenomatous polyposis coli

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Liganded androgen receptor interaction with beta-catenin: nuclear co-localization and modulation of transcriptional activity in neuronal cells

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Ligand-dependent inhibition of beta-catenin/TCF signaling by androgen receptor

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Beta-catenin binds to the activation function 2 region of the androgen receptor and modulates the effects of the N-terminal domain and TIF2 on ligand-dependent transcription

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Cross-regulation of beta-catenin-LEF/TCF and retinoid signaling pathways

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Vitamin D(3) promotes the differentiation of colon carcinoma cells by the induction of E-cadherin and the inhibition of beta-catenin signaling.

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Progression of metastatic human prostate cancer to androgen independence in immunodeficient SCID mice

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Bicalutamide functions as an androgen receptor antagonist by assembly of a transcriptionally inactive receptor

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Identification of c- MYC as a Target of the APC Pathway

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

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Differential modulation of transcriptional activity of estrogen receptors by direct protein-protein interactions with the T cell factor family of transcription factors

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Beta-catenin regulates expression of cyclin D1 in colon carcinoma cells

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The beta-catenin/TCF-4 complex imposes a crypt progenitor phenotype on colorectal cancer cells

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Inhibition of androgen receptor-mediated transcription by amino-terminal enhancer of split

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Cyproterone acetate--mechanism of action and clinical effectiveness in prostate cancer treatment

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AML3/CBFalpha1 is required for androgen-specific activation of the enhancer of the mouse sex-limited protein (Slp) gene

21 January 2018

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Oct-1 preferentially interacts with androgen receptor in a DNA-dependent manner that facilitates recruitment of SRC-1

21 January 2018

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Coregulatory proteins in steroid hormone receptor action: the role of chromatin high mobility group proteins HMG-1 and -2

21 January 2018

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release_spxqp53zmngajn52gjm6a4tsq4

21 January 2018

Identifiers

DOI

10.1074/JBC.M301208200

0 references

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/spxqp53zmngajn52gjm6a4tsq4