Mdm2 Promotes Odontoblast-like Differentiation by Ubiquitinating Dlx3 and p53.
cell differentiation
dentinogenesis
molecular biology
post-translational modifications
tooth development
transcription factor(s)
Journal
Journal of dental research
ISSN: 1544-0591
Titre abrégé: J Dent Res
Pays: United States
ID NLM: 0354343
Informations de publication
Date de publication:
03 2020
03 2020
Historique:
pubmed:
19
12
2019
medline:
11
11
2020
entrez:
19
12
2019
Statut:
ppublish
Résumé
Dentin is an important structural component of the tooth. Odontoblast differentiation is an essential biological process that guarantees normal dentin formation, which is precisely regulated by various proteins. Murine double minute 2 (Mdm2) is an E3 ubiquitin ligase, and it plays a pivotal role in the differentiation of different cell types, such as osteoblasts and myoblasts. However, whether Mdm2 plays a role in odontoblast differentiation remains unknown. Here, we investigated the spatiotemporal expression of Mdm2 by immunostaining and found that Mdm2 was highly expressed in the odontoblasts and slightly in the dental papilla cells of mouse incisors and molars. Gene knockdown and overexpression experiments verified that Mdm2 promoted the odontoblast-like differentiation of mouse dental papilla cells (mDPCs). Intranuclear colocalization and physical interaction between Mdm2 and distal-less 3 (Dlx3), a transcription factor important for odontoblast differentiation, was found during the odontoblast-like differentiation of mDPCs by double immunofluorescence and immunoprecipitation. Mdm2 was proved to monoubiquitinate Dlx3, which enhanced the expression of Dlx3 target gene
Identifiants
pubmed: 31847675
doi: 10.1177/0022034519893672
doi:
Substances chimiques
Distal-less homeobox proteins
0
Homeodomain Proteins
0
Transcription Factors
0
Tumor Suppressor Protein p53
0
Mdm2 protein, mouse
EC 2.3.2.27
Proto-Oncogene Proteins c-mdm2
EC 2.3.2.27
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM