Abstract | OBJECTIVE: SUBJECTS AND METHODS: Whole exome and Sanger sequencing were employed to identify mutations. Physical characteristics of the teeth were examined. Pulp cells' behaviours including cell proliferation, colony-forming unit, osteogenic differentiation, pluripotent markers, and mesenchymal stem cell markers were investigated. RESULTS: The proband had opalescent brown primary teeth with extensive loss of enamel. Mutation analysis revealed a novel heterozygous 4-bp deletion, c.1915_1918delAAGT (p.K639QfsX674), in exon 5 of the DSPP associated with DGI. Analysis of the extracted primary incisor demonstrated a decrease in brightness but an increase in yellow and red chroma. The dentin showed reduced mineral density. The dentinal tubules were present in the predentin, but progressively collapsed in the dentin. The pulp cells exhibited markedly reduced CD105 expression, decreased cell proliferation, and smaller colony-forming units. CONCLUSIONS: We identified a novel mutation in the DSPP gene which disturbed dentin characteristics and pulp cells' behaviours. Our study expands the mutation spectrum and understanding of pathologic dentin phenotypes related to the frameshift deletion in the dentin phosphoprotein (DPP) region of the DSPP gene.
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Authors | T Porntaveetus, T Osathanon, N Nowwarote, P Pavasant, C Srichomthong, K Suphapeetiporn, V Shotelersuk |
Journal | Oral diseases
(Oral Dis)
Vol. 24
Issue 4
Pg. 619-627
(May 2018)
ISSN: 1601-0825 [Electronic] Denmark |
PMID | 29117466
(Publication Type: Case Reports, Journal Article)
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Copyright | © 2017 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd. |
Chemical References |
- ENG protein, human
- Endoglin
- Extracellular Matrix Proteins
- Phosphoproteins
- Sialoglycoproteins
- dentin sialophosphoprotein
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Topics |
- Base Sequence
- Cell Differentiation
(genetics)
- Cell Proliferation
(genetics)
- Cells, Cultured
- Child, Preschool
- Colony-Forming Units Assay
- Dental Pulp
(pathology, physiopathology, ultrastructure)
- Dentin
(physiopathology, ultrastructure)
- Dentinogenesis Imperfecta
(genetics)
- Endoglin
(metabolism)
- Extracellular Matrix Proteins
(genetics)
- Humans
- Male
- Pedigree
- Phenotype
- Phosphoproteins
(genetics)
- Sequence Deletion
- Sialoglycoproteins
(genetics)
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