Evidence map›Paper›PMID 25274628›Full record

ArticleThe Journal of biological chemistry2014

An atypical canonical bone morphogenetic protein (BMP) signaling pathway regulates Msh homeobox 1 (Msx1) expression during odontogenesis.

Guobin Yang, Guohua Yuan, Wenduo Ye, Ken W Y Cho, YiPing Chen

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
2.0field-weighted citation impact, top 14% 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

20 citing papers in PubMed, 32 citations in OpenAlex.

  1. Article
  2. Article
  3. Regenerative Glycopeptide Scaffolds Enhance BMP-4 Activity To Treat Pediatric Glioma.Regenerative engineering and translational medicine · 2025
    Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Dental Pulp Stem Cells: Advances to Applications.Stem cells and cloning : advances and applications · 2020
    Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Expression of Sox genes in tooth development.The International journal of developmental biology · 2015
    Article
  19. Article
  20. Depletion of MEIS2 inhibits osteogenic differentiation potential of human dental stem cells.International journal of clinical and experimental medicine · 2015
    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

5 authors at 3 institutions in 2 countries.

Guobin YangFrom the State Key Laboratory Breeding Base of Basic Science of Stomatology and Key Laboratory for Oral Biomedicine of Ministry of Education, School and Hospital of Stomatology, Wuhan University, Wuhan 430079, Hubei Province, China, the Department of Cell and Molecular Biology, Tulane University, New Orleans, Louisiana 70118, and.
Guohua YuanFrom the State Key Laboratory Breeding Base of Basic Science of Stomatology and Key Laboratory for Oral Biomedicine of Ministry of Education, School and Hospital of Stomatology, Wuhan University, Wuhan 430079, Hubei Province, China, the Department of Cell and Molecular Biology, Tulane University, New Orleans, Louisiana 70118, and.
Wenduo Yethe Department of Cell and Molecular Biology, Tulane University, New Orleans, Louisiana 70118, and.
Ken W Y Chothe Department of Developmental and Cell Biology, School of Biological Sciences, University of California, Irvine, California 92697.
YiPing Chenthe Department of Cell and Molecular Biology, Tulane University, New Orleans, Louisiana 70118, and ychen@tulane.edu.
Tulane University · USUniversity of California, Irvine · USWuhan University · CN

Funding

Growth Factor Signaling in Mouse PalatogensisR01DE014044 · NIDCR · TULANE UNIVERSITY OF LOUISIANA · PI CHEN, YIPING · 2002 to 2013
$3.4M
Role of BMP and Wnt signaling in early tooth developmentR01DE024152 · NIDCR · TULANE UNIVERSITY OF LOUISIANA · PI CHEN, YIPING · 2014 to 2018
$1.9M
NIDCR NIH HHS R01 DE014044NIDCR NIH HHS R01DE014044NIDCR NIH HHS R01 DE024152NIDCR NIH HHS R01DE024152
6 · The paper itself

Abstract

Bone morphogenetic protein (BMP) signaling plays an essential role in early tooth development, evidenced by disruption of BMP signaling leading to an early arrested tooth development. Despite being a central mediator of BMP canonical signaling pathway, inactivation of Smad4 in dental mesenchyme does not result in early developmental defects. In the current study, we investigated the mechanism of receptor-activated Smads (R-Smads) and Smad4 in the regulation of the odontogenic gene Msx1 expression in the dental mesenchyme. We showed that the canonical BMP signaling is not operating in the early developing tooth, as assessed by failed activation of the BRE-Gal transgenic allele and the absence of phospho-(p)Smad1/5/8-Smad4 complexes. The absence of pSmad1/5/8-Smad4 complex appeared to be the consequence of saturation of Smad4 by pSmad2/3 in the dental mesenchyme as knockdown of Smad2/3 or overexpression of Smad4 led to the formation of pSmad1/5/8-Smad4 complexes and activation of canonical BMP signaling in dental mesenchymal cells. We showed that Smad1/5 but not Smad4 are required for BMP-induced expression of Msx1 in dental mesenchymal cells. We further presented evidence that in the absence of Smad4, BMPs are still able to induce pSmad1/5/8 nuclear translocation and their binding to the Msx1 promoter directly in dental mesenchymal cells. Our results demonstrate the functional operation of an atypical canonical BMP signaling (Smad4-independent and Smad1/5/8-dependent) pathway in the dental mesenchyme during early odontogenesis, which may have general implication in the development of other organs.

Indexed as

Gene Expression Regulation, DevelopmentalSignal TransductionActive Transport, Cell NucleusAllelesAnimalsBone Morphogenetic ProteinsCell NucleusExonsGenes, HomeoboxMesodermMiceMice, TransgenicMSX1 Transcription FactorOdontogenesisRNA InterferenceSmad1 ProteinBone Morphogenetic ProteinsMsx1 protein, mouseMSX1 Transcription FactorSmad1 ProteinSmad1 protein, mouseSmad4 ProteinSmad4 protein, mouseSmad5 ProteinSmad5 protein, mouseTransforming Growth Factor beta1Bone Morphogenetic Protein (BMP)Cell SignalingCraniofacial DevelopmentDental MesenchymeGene ExpressionMsx1Smad4-independentSMAD Transcription Factor

Identifiers

PMID25274628
PMCPMC4223347
OpenAlexW2089066281

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.