Evidence map›Paper›PMID 17785445›Full record

ArticleMolecular and cellular biology2007

PITX2 and beta-catenin interactions regulate Lef-1 isoform expression.

Melanie Amen, Xiaoming Liu, Usha Vadlamudi, Gabriela Elizondo, Evan Diamond, John F Engelhardt, Brad A Amendt

Open access · greenAbstract read
In one paragraph

Article in Molecular and cellular biology, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 50 papers.

0numbers the graph read from it
0cells of the map it votes in
50citing papers in PubMed
3.1field-weighted citation impact, top 8% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

50 citing papers in PubMed, 77 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Research Progress of LEF1 Gene in Malignant Tumors.Clinical Medicine Insights. Oncology · 2025
    Review
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  7. Tooth number abnormality: from bench to bedside.International journal of oral science · 2023
    Review
  8. Article
  9. Article
  10. Development (Cambridge, England) · 2020
    Article
  11. Ectodermal Organ Development Is Regulated by aFrontiers in physiology · 2020
    Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors at 4 institutions in 2 countries.

Melanie AmenTexas A&M Health Science Center, Institute of Biosciences and Technology, 2121 W. Holcombe Boulevard, Houston, TX 77030, USA.
Xiaoming Liu
Usha Vadlamudi
Gabriela Elizondo
Evan Diamond
John F Engelhardt
Brad A Amendt
Texas A&M Health Science Center · USUniversity of Iowa · USTecnológico de Monterrey · MXUniversity of Tulsa · US

Funding

Vector Core-Core 2P30DK054759 · NIDDK · UNIVERSITY OF IOWA · PI Alejandro Antonio Pezzulo · 1998 to 2026
$30.5M
Molecular Mechanisms of PITX2 During Craniofacial DevelopmentR01DE013941 · NIDCR · UNIVERSITY OF TULSA · PI AMENDT, BRAD A · 2000 to 2013
$4.2M
Biology of submucosal gland stem cells in the airwayR37DK047967 · NIDDK · UNIVERSITY OF IOWA · PI ENGELHARDT, JOHN F · 2005 to 2014
$3.8M
NIDCR NIH HHS DE 13941NIDCR NIH HHS R01 DE013941NIDDK NIH HHS P30 DK054759NIDDK NIH HHS R37 DK047967
6 · The paper itself

Abstract

Lef-1 and PITX2 function in the Wnt signaling pathway by recruiting and interacting with beta-catenin to activate target genes. Chromatin immunoprecipitation (ChIP) assays identified the Lef-1 promoter as a PITX2 downstream target. Transgenic mice expressing LacZ driven by the 2.5-kb LEF-1 promoter demonstrated expression in the tooth epithelium correlated with endogenous Lef-1 FL epithelial expression. PITX2 isoforms regulate the LEF-1 promoter, and beta-catenin synergistically enhanced activation of the LEF-1 promoter in combination with PITX2 and Lef-1 isoforms. PITX2 enhances endogenous expression of the full-length beta-catenin-dependent Lef-1 isoform (Lef-1 FL) while decreasing expression of the N-terminally truncated beta-catenin-independent isoform. Our research revealed a novel interaction between PITX2, Lef-1, and beta-catenin in which the Lef-1 beta-catenin binding domain is dispensable for its interaction with PITX2. PITX2 interacts with two sites within the Lef-1 protein. Furthermore, beta-catenin interacts with the PITX2 homeodomain and Lef-1 interacts with the PITX2 C-terminal tail. Lef-1 and beta-catenin interact simultaneously and independently with PITX2 through two different sites to regulate PITX2 transcriptional activity. These data support a role for PITX2 in cell proliferation, migration, and cell division through differential Lef-1 isoform expression and interactions with Lef-1 and beta-catenin.

Indexed as

Animalsbeta CateninCHO CellsCricetinaeCricetulusFemaleGene Expression Regulation, DevelopmentalHomeobox Protein PITX2Homeodomain ProteinsHumansIncisorLymphoid Enhancer-Binding Factor 1MaleMiceMice, Inbred C57BLMutationbeta CateninHomeobox Protein PITX2Homeodomain ProteinsLymphoid Enhancer-Binding Factor 1Protein IsoformsTranscription Factors

Identifiers

PMID17785445
PMCPMC2169058
OpenAlexW2161778191

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.