# Genome-wide selection analysis identifies genes associated with mandibular defects in Duolang sheep

**Authors:** Hang Cao, Qiuming Chen, Ling-Ling Liu, Wu-Jun Liu

PMC · DOI: 10.3389/fvets.2025.1714754 · Frontiers in Veterinary Science · 2026-01-05

## TL;DR

This study identifies genes linked to facial structure defects in Duolang sheep, offering insights for genetic improvement and skeletal development research.

## Contribution

The study identifies novel candidate genes associated with brachycephaly in Duolang sheep using genome-wide selection analysis.

## Key findings

- Affected Duolang sheep had shorter maxillae and longer mandibles compared to controls.
- Genomic analysis identified candidate genes like MTX2, FGF12, and IGF linked to skeletal development.
- The findings suggest a genetic basis for brachycephaly in this breed.

## Abstract

Brachycephaly is characterized by a conspicuously shortened craniofacial structure. While it is a defining trait in certain species such as Bulldogs, Persian cats, Niata cattle, Anglo-Nubian goats, and Middle White pigs, it may also represent a pathological condition. In Duolang sheep, brachycephaly is strikingly pronounced and may arise from distinct genetic and developmental mechanisms linked to breed history. This condition, often accompanied by mandibular prognathism, predisposes affected animals to health problems including brachycephalic airway obstruction syndrome, nasal blockage with dyspnea, and feeding difficulties. Duolang sheep, a dominant indigenous breed in southern Xinjiang, China, comprise approximately two million individuals, nearly 10% of which exhibit this heritable defect. Such a high prevalence poses a significant challenge to genetic improvement programs in local populations. Elucidating the genetic basis of this phenotype and identifying candidate genes is therefore essential.

To characterize the craniofacial phenotype, we obtained X-ray measurements of maxillary length, mandibular length, and incisor angle. Affected sheep displayed significantly shorter maxillae and longer mandibles compared with controls (p < 0.05), whereas incisor angle showed no significant difference. Here, we performed whole-genome resequencing of two phenotypically distinct Duolang sheep cohorts and analyzed genomic architecture and variation patterns using a selective sweep approach.

Candidate regions under strong selection were identified by Fst and π-ratio analyses. Gene annotation revealed functionally relevant candidates associated with skeletal growth and development (MTX2, FGF12, IGF, PPARGC1A, LIPC, LY86, and IL33).

These findings provide new insights into the genetic basis of brachycephaly in Duolang sheep and offer strategies for genetic improvement, contributing to broader research on skeletal development and growth regulation in livestock.

## Linked entities

- **Genes:** MTX2 (metaxin 2) [NCBI Gene 10651], FGF12 (fibroblast growth factor 12) [NCBI Gene 2257], IGF1 (insulin like growth factor 1) [NCBI Gene 3479], PPARGC1A (PPARG coactivator 1 alpha) [NCBI Gene 10891], LIPC (lipase C, hepatic type) [NCBI Gene 3990], LY86 (lymphocyte antigen 86) [NCBI Gene 9450], IL33 (interleukin 33) [NCBI Gene 90865]

## Full-text entities

- **Genes:** MYO5A [NCBI Gene 101105758], BMP3 [NCBI Gene 487826], FGF10 [NCBI Gene 443074], RUNX2 [NCBI Gene 101115489], FOXL2 [NCBI Gene 106990809], IL33 [NCBI Gene 101116705], ACTN1 [NCBI Gene 101122194], FGF9 [NCBI Gene 101116844], insulin [NCBI Gene 105613195], FGF8 [NCBI Gene 101113716], SMOC2 [NCBI Gene 101116580], LIPC [NCBI Gene 101116992], BMP3 [NCBI Gene 101108049], PPARGC1A [NCBI Gene 443270], Akt [NCBI Gene 100294652], GABRG3 [NCBI Gene 101108521], FGF12 [NCBI Gene 100302340], FST [NCBI Gene 443323], LY86 [NCBI Gene 101108087], SMOC2 (SPARC related modular calcium binding 2) [NCBI Gene 476270], MTX2 [NCBI Gene 101105801], FGF18 [NCBI Gene 780460], RORA [NCBI Gene 101102986], COL1A1 [NCBI Gene 443483]
- **Diseases:** mandibular hypoplasia (MESH:D008336), BOAS (MESH:D000402), cleidocranial dysplasia (MESH:D002973), prognathism (MESH:D011378), Brachycephaly (MESH:D003398), Depression (MESH:D003866), nasal blockage (MESH:D015508), Mandibular prognathism (MESH:D008313), respiratory distress (MESH:D012128), osteogenesis imperfecta (MESH:D010013), facial dysmorphism (MESH:C565579), Duolang sheep (MESH:D012757), dyspnea (MESH:D004417), skull deformities (MESH:D012888), facial retrusion (MESH:D063173), mandibular anomalies (MESH:D008338), infection (MESH:D007239), L-LL (MESH:D007926), Genetic defects (MESH:D030342), craniofacial defects (MESH:D019465), cranial development defects (MESH:D002658), growth retardation (MESH:D006130), obstructive respiratory syndrome (MESH:D012131), cancer (MESH:D009369)
- **Chemicals:** EDTA (MESH:D004492), chloroform (MESH:D002725), phenol (MESH:D019800), agarose (MESH:D012685)
- **Species:** Mus musculus (house mouse, species) [taxon 10090], Sus scrofa (pig, species) [taxon 9823], Ovis aries (domestic sheep, species) [taxon 9940], Bos taurus (bovine, species) [taxon 9913], Homo sapiens (human, species) [taxon 9606], HC [taxon 11103], Canis lupus familiaris (dog, subspecies) [taxon 9615], Capra hircus (domestic goat, species) [taxon 9925]
- **Mutations:** c.543 + 1G > T

## Full text

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## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12838256/full.md

## References

41 references — full list in the complete paper: https://tomesphere.com/paper/PMC12838256/full.md

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Source: https://tomesphere.com/paper/PMC12838256