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A Mutation in CACNA1S Is Associated with Multiple Supernumerary Cusps and Root Maldevelopment
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Metadata
Document Title
A Mutation in CACNA1S Is Associated with Multiple Supernumerary Cusps and Root Maldevelopment
Author
Kantaputra P. Leelaadisorn N. Hatsadaloi A. Quarto N. Intachai W. Tongsima S. Kawasaki K. Ohazama A. Ngamphiw C. Wiriyakijja P.
Affiliations
Center of Excellence in Medical Genetics Research Faculty of Dentistry Chiang Mai University Chiang Mai 50200 Thailand; Division of Pediatric Dentistry Department of Orthodontics and Pediatric Dentistry Faculty of Dentistry Chiang Mai University Chiang Mai 50200 Thailand; Dental Department Rot-et Hospital Roi-et 45000 Thailand; Dental Home Clinic Khon Kaen 40000 Thailand; Division of Plastic and Reconstructive Surgery Department of Surgery School of Medicine Stanford University Stanford CA 94305 United States; National Biobank of Thailand National Science and Technology Development Agency (NSTDA) Thailand Science Park Pathum Thani 12120 Thailand; Division of Oral Anatomy Faculty of Dentistry & Graduate School of Medical and Dental Sciences Niigata University Niigata 951-8514 Japan; Department of Oral Medicine Faculty of Dentistry Chulalongkorn University Bangkok 10330 Thailand; Avatar Biotechnologies for Oral Health and Healthy Longevity Research Unit Chulalongkorn University Bangkok 10330 Thailand
Type
Article
Source Title
Diagnostics
ISSN
20754418
Year
2023
Volume
13
Issue
5
Open Access
All Open Access Gold Green
Publisher
Multidisciplinary Digital Publishing Institute (MDPI)
DOI
10.3390/diagnostics13050895
Abstract
Background: Enamel knots and Hertwig epithelial root sheath (HERS) regulate the growth and folding of the dental epithelium which subsequently determines the final form of tooth crown and roots. We would like to investigate the genetic etiology of seven patients affected with unique clinical manifestations including multiple supernumerary cusps single prominent premolars and single-rooted molars. Methods: Oral and radiographic examination and whole-exome or Sanger sequencing were performed in seven patients. Immunohistochemical study during early tooth development in mice was performed. Results: A heterozygous variant (c. 865A>G; p.Ile289Val) in CACNA1S was identified in all the patients but not in an unaffected family member and control. Immunohistochemical study showed high expression of Cacna1s in the secondary enamel knot. Conclusions: This CACNA1S variant seemed to cause impaired dental epithelial folding; too much folding in the molars and less folding in the premolars; and delayed folding (invagination) of HERS which resulted in single-rooted molars or taurodontism. Our observation suggests that the mutation in CACNA1S might disrupt calcium influx resulting in impaired dental epithelium folding and subsequent abnormal crown and root morphology. ? 2023 by the authors.
Industrial Classification
Knowledge Taxonomy Level 1
Knowledge Taxonomy Level 2
Knowledge Taxonomy Level 3
License
CC BY
Rights
Authors
Publication Source
WOS