BMPR2 Variants Underlie Nonsyndromic Oligodontia

• Published in: International journal of molecular sciences Vol. 24; no. 2; p. 1648
• Main Authors: Zheng, Jinglei, Liu, Haochen, Yu, Miao, Lin, Bichen, Sun, Kai, Liu, Hangbo, Feng, Hailan, Liu, Yang, Han, Dong
• Format: Journal Article
• Language: English
• Published: Switzerland MDPI AG 13-01-2023; MDPI
• Subjects: Amino acids; Animals; Anodontia - genetics; Anodontia - metabolism; BMP-SMAD1/5/8 signaling; BMPR2; Bone density; Bone morphogenetic protein receptor type II; Bone Morphogenetic Protein Receptors, Type II - genetics; Bone Morphogenetic Protein Receptors, Type II - metabolism; Dental enamel; Electrocardiography; Enamel; Epithelium; Etiology; Families & family life; Functional analysis; Genes; genetics; Haploinsufficiency; Heterozygosity; Humans; Hybridization; Hypertension; Kinases; Mice; Mutation; nonsyndromic oligodontia; Plasmids; Proteins; Pulmonary arteries; Teeth; variants; BMP-SMAD1/5/8 signaling; BMPR2; genetics; variants; nonsyndromic oligodontia
• ISSN: 1422-0067; 1661-6596; 1422-0067
• DOI: 10.3390/ijms24021648

Oligodontia manifests as a congenital reduction in the number of permanent teeth. Despite the major efforts that have been made, the genetic etiology of oligodontia remains largely unknown. Bone morphogenetic protein receptor type 2 (BMPR2) variants have been associated with pulmonary arterial hypertension (PAH). However, the genetic significance of BMPR2 in oligodontia has not been previously reported. In the present study, we identified a novel heterozygous variant (c.814C > T; p.Arg272Cys) of BMPR2 in a family with nonsyndromic oligodontia by performing whole-exome sequencing. In addition, we identified two additional heterozygous variants (c.1042G > A; p.Val348Ile and c.1429A > G; p.Lys477Glu) among a cohort of 130 unrelated individuals with nonsyndromic oligodontia by performing Sanger sequencing. Functional analysis demonstrated that the activities of phospho-SMAD1/5/8 were significantly inhibited in BMPR2-knockout 293T cells transfected with variant-expressing plasmids, and were significantly lower in BMPR2 heterozygosity simulation groups than in the wild-type group, indicating that haploinsufficiency may represent the genetic mechanism. RNAscope in situ hybridization revealed that BMPR2 transcripts were highly expressed in the dental papilla and adjacent inner enamel epithelium in mice tooth germs, suggesting that BMPR2 may play important roles in tooth development. Our findings broaden the genetic spectrum of oligodontia and provide clinical and genetic evidence supporting the importance of BMPR2 in nonsyndromic oligodontia.