Evidence map›Paper›PMID 25101640›Full record

ArticlePloS one2014

Characterization of novel MSX1 mutations identified in Japanese patients with nonsyndromic tooth agenesis.

Seishi Yamaguchi, Junichiro Machida, Munefumi Kamamoto, Masashi Kimura, Akio Shibata, Tadashi Tatematsu, Hitoshi Miyachi, Yujiro Higashi, Peter Jezewski, Atsuo Nakayama and 2 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.9field-weighted citation impact, top 15% 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

13 citing papers in PubMed, 29 citations in OpenAlex.

  1. NovelChildren (Basel, Switzerland) · 2024
    Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. The role of external aetiological factors in dental anomalies in non-syndromic cleft lip and palate patients.European archives of paediatric dentistry : official journal of the European Academy of Paediatric Dentistry · 2019
    Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. 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

12 authors at 5 institutions in 2 countries.

Seishi YamaguchiDepartment of Maxillofacial Surgery, School of Dentistry, Aichi-Gakuin University, Nagoya, Aichi, Japan; Department of Dentistry and Oral Surgery, Aichi Children's Health and Medical Center, Obu, Aichi, Japan; Department of Perinatology, Institute for Developmental Research, Aichi Human Service Center, Kasugai, Aichi, Japan.
Junichiro MachidaDepartment of Maxillofacial Surgery, School of Dentistry, Aichi-Gakuin University, Nagoya, Aichi, Japan; Department of Oral and Maxillofacial Surgery, Toyota Memorial Hospital, Toyota, Aichi, Japan.
Munefumi KamamotoDepartment of Maxillofacial Surgery, School of Dentistry, Aichi-Gakuin University, Nagoya, Aichi, Japan; Department of Oral and Maxillofacial Surgery, Japanese Red Cross Society Himeji Hospital, Himeji, Hyogo, Japan.
Masashi KimuraDepartment of Maxillofacial Surgery, School of Dentistry, Aichi-Gakuin University, Nagoya, Aichi, Japan; Department of Perinatology, Institute for Developmental Research, Aichi Human Service Center, Kasugai, Aichi, Japan.
Akio ShibataDepartment of Maxillofacial Surgery, School of Dentistry, Aichi-Gakuin University, Nagoya, Aichi, Japan; Department of Perinatology, Institute for Developmental Research, Aichi Human Service Center, Kasugai, Aichi, Japan.
Tadashi TatematsuDepartment of Maxillofacial Surgery, School of Dentistry, Aichi-Gakuin University, Nagoya, Aichi, Japan; Department of Perinatology, Institute for Developmental Research, Aichi Human Service Center, Kasugai, Aichi, Japan.
Hitoshi MiyachiDepartment of Maxillofacial Surgery, School of Dentistry, Aichi-Gakuin University, Nagoya, Aichi, Japan.
Yujiro HigashiDepartment of Perinatology, Institute for Developmental Research, Aichi Human Service Center, Kasugai, Aichi, Japan.
Peter JezewskiDepartment of Periodontology, University of Alabama at Birmingham School of Dentistry, Institute of Oral Health Research, Birmingham, Alabama, United States of America.
Atsuo NakayamaDepartment of Embryology, Institute for Developmental Research, Aichi Human Service Center, Kasugai, Aichi, Japan.
Kazuo ShimozatoDepartment of Maxillofacial Surgery, School of Dentistry, Aichi-Gakuin University, Nagoya, Aichi, Japan.
Yoshihito TokitaDepartment of Maxillofacial Surgery, School of Dentistry, Aichi-Gakuin University, Nagoya, Aichi, Japan; Department of Perinatology, Institute for Developmental Research, Aichi Human Service Center, Kasugai, Aichi, Japan.
Aichi Gakuin University · JPAichi Human Service Center · JPHimeji Red Cross Hospital · JPToyota Memorial Hospital · JPUniversity of Alabama at Birmingham · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Since MSX1 and PAX9 are linked to the pathogenesis of nonsyndromic tooth agenesis, we performed detailed mutational analysis of these two genes sampled from Japanese patients. We identified two novel MSX1 variants with an amino acid substitution within the homeodomain; Thr174Ile (T174I) from a sporadic hypodontia case and Leu205Arg (L205R) from a familial oligodontia case. Both the Thr174 and Leu205 residues in the MSX1 homeodomain are highly conserved among different species. To define possible roles of mutations at these amino acids in the pathogenesis of nonsyndromic tooth agenesis, we performed several functional analyses. It has been demonstrated that MSX1 plays a pivotal role in hard tissue development as a suppressor for mesenchymal cell differentiation. To evaluate the suppression activity of the variants in mesenchymal cells, we used the myoD-promoter, which is one of convenient reporter assay system for MSX1. Although the gene products of these MSX1 variants are stable and capable of normal nuclear localization, they do not suppress myoD-promoter activity in differentiated C2C12 cells. To clarify the molecular mechanisms underlying our results, we performed further analyses including electrophoretic mobility shift assays, and co-immunoprecipitation assays to survey the molecular interactions between the mutant MSX1 proteins and the oligonucleotide DNA with MSX1 consensus binding motif or EZH2 methyltransferase. Since EZH2 is reported to interact with MSX1 and regulate MSX1 mediated gene suppression, we hypothesized that the T174I and L205R substitutions would impair this interaction. We conclude from the results of our experiments that the DNA binding ability of MSX1 is abolished by these two amino acid substitutions. This illustrates a causative role of the T174I and L205R MSX1 homeodomain mutations in tooth agenesis, and suggests that they may influence cell proliferation and differentiation resulting in lesser tooth germ formation in vivo.

Indexed as

Amino Acid SubstitutionAmino Acid SequenceAnodontiaBinding SitesConserved SequenceDNA Mutational AnalysisElectrophoretic Mobility Shift AssayEnhancer of Zeste Homolog 2 ProteinFemaleGene Expression RegulationHumansJapanMaleMolecular Sequence DataMSX1 Transcription FactorPedigreeEnhancer of Zeste Homolog 2 ProteinEZH2 protein, humanMSX1 protein, humanMSX1 Transcription FactorPolycomb Repressive Complex 2

Identifiers

PMID25101640
PMCPMC4125152
OpenAlexW2065597789

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.