# Investigating possible shared single nucleotide polymorphisms in isolated oral cleft and non-cleft facial morphology

**Authors:** Erika Calvano Küchler, Michelle Nascimento Meger, Bruna Correia Rauta Pires, Svenja Beisel-Memmert, Daniel Hemming, Ricardo D. Coletta, Rafaela Scariot, Mírian Aiko Nakane Matsumoto, Maria Angelica Hueb de Menezes Oliveira, Christian Kirschneck, Bianca Cavalcante-Leão

PMC · DOI: 10.3389/fdmed.2025.1546295 · Frontiers in Dental Medicine · 2025-04-15

## TL;DR

This study explores how genetic variations linked to oral clefts may also influence normal facial development.

## Contribution

The study provides evidence that SNPs associated with oral clefts are also linked to facial morphology in healthy individuals.

## Key findings

- The SNP rs17563 in BMP4 is associated with lip proportion differences based on genotype.
- The SNP rs1533767 in WNT11 is linked to multiple facial measurements with statistical significance.
- Oral cleft-associated SNPs are shown to influence normal facial development patterns.

## Abstract

Facial morphogenesis is regulated by several cellular interactions that are mediated by numerous morphogenetic signals. Based on the existing evidence, we hypothesize that oral cleft-associated single nucleotide polymorphisms (SNPs) are involved in the normal range of human face development. Therefore, this study aimed to investigate the association between SNPs in oral cleft-related genes and variations in the normal range of facial morphology.

A sample of healthy Brazilian teenagers (aged between 11 and 18 years old) were screened and collected. Frontal facial digitized photographs from orthodontic records were used to determine phenotypes, while the DNA extracted from saliva samples was used to investigate the candidate SNPs. Five oral cleft-associated SNPs in BMP2 (rs235768), BMP4 (rs17563), WNT3A (rs708111), WNT11 (rs1533767), and RUNX2 (rs1200425) were selected, and allelic discrimination analysis was performed using real-time PCR.

A total of 58 individuals (27 boys and 31 girls) were included. The facial landmarks used for the facial measurements were the trichion (Tr), glabella (G), nassion (N), subnasale (Sn), labrale superior (Ls), labrale inferior (Li), gnathion (Gn), cheilon (Ch), and zygoma (Zg). rs17563 in BMP4 was associated with lip proportion, in which individuals with the homozygous GG genotype had a higher Ch-Ch:Ls-Li proportion than the heterozygous AG genotype (p = 0.034). rs1533767 in WNT11 was associated with G-Sn:Sn-Gn (p = 0.028), N-Gn:Sn-Gn (p = 0.035), and Sn-Gn:Tr-Gn (p = 0.039).

Our study supported the hypothesis that oral cleft-associated SNPs are involved in the normal range of human facial morphology.

## Linked entities

- **Genes:** BMP2 (bone morphogenetic protein 2) [NCBI Gene 650], BMP4 (bone morphogenetic protein 4) [NCBI Gene 652], WNT3A (Wnt family member 3A) [NCBI Gene 89780], WNT11 (Wnt family member 11) [NCBI Gene 7481], RUNX2 (RUNX family transcription factor 2) [NCBI Gene 860]

## Full-text entities

- **Genes:** WNT3A (Wnt family member 3A) [NCBI Gene 89780], RUNX2 (RUNX family transcription factor 2) [NCBI Gene 860] {aka AML3, CBF-alpha-1, CBFA1, CCD, CCD1, CLCD}, BMP2 (bone morphogenetic protein 2) [NCBI Gene 650] {aka BDA2, BMP2A, SSFSC, SSFSC1}, WNT11 (Wnt family member 11) [NCBI Gene 7481] {aka HWNT11}, BMP4 (bone morphogenetic protein 4) [NCBI Gene 652] {aka BMP2B, BMP2B1, MCOPS6, OFC11, ZYME}
- **Diseases:** oral cleft (MESH:D002971), lip (MESH:D008047)
- **Species:** Homo sapiens (human, species) [taxon 9606]
- **Mutations:** rs1533767, rs17563, rs235768, rs708111, rs1200425

## Full text

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## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12037601/full.md

## References

28 references — full list in the complete paper: https://tomesphere.com/paper/PMC12037601/full.md

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Source: https://tomesphere.com/paper/PMC12037601