» Articles » PMID: 35372529

Identification of Key Candidate Genes for Beak Length Phenotype by Whole-Genome Resequencing in Geese

Overview
Journal Front Vet Sci
Date 2022 Apr 4
PMID 35372529
Authors
Affiliations
Soon will be listed here.
Abstract

The domestic goose is an important economic animal in agriculture and its beak, a trait with high heritability, plays an important role in promoting food intake and defending against attacks. In this study, we sequenced 772 420-day-old Xingguo gray geese (XGG) using a low-depth (~1 ×) whole-genome resequencing strategy. We detected 12,490,912 single nucleotide polymorphisms (SNPs) using the standard GATK and imputed with STITCH. We then performed a genome-wide association study on the beak length trait in XGG. The results indicated that 57 SNPs reached genome-wide significance levels for the beak length trait and were assigned to seven genes, including , and . The different genotypes of the most significant SNP (top SNP), which was located upstream of and explained 7.24% of the phenotypic variation in beak length, showed significant differences in beak length. Priority-based significance analysis concluded that , and genes in the most significant quantitative trait locus interval were the most plausible positional and functional candidate genes for beak length development in the XGG population. These findings not only enhance our understanding of the genetic mechanism of the beak length phenotype in geese, but also lay the foundation for further studies to facilitate the genetic selection of traits in geese.

Citing Articles

Genome-Wide Association Studies, Runs of Homozygosity Analysis, and Copy Number Variation Detection to Identify Reproduction-Related Genes in Bama Xiang Pigs.

Mo J, Lu Y, Zhu S, Feng L, Qi W, Chen X Front Vet Sci. 2022; 9:892815.

PMID: 35711794 PMC: 9195146. DOI: 10.3389/fvets.2022.892815.

References
1.
Lamichhaney S, Berglund J, Almen M, Maqbool K, Grabherr M, Martinez-Barrio A . Evolution of Darwin's finches and their beaks revealed by genome sequencing. Nature. 2015; 518(7539):371-5. DOI: 10.1038/nature14181. View

2.
Fagerberg L, Hallstrom B, Oksvold P, Kampf C, Djureinovic D, Odeberg J . Analysis of the human tissue-specific expression by genome-wide integration of transcriptomics and antibody-based proteomics. Mol Cell Proteomics. 2013; 13(2):397-406. PMC: 3916642. DOI: 10.1074/mcp.M113.035600. View

3.
Abramyan J, Richman J . Craniofacial development: discoveries made in the chicken embryo. Int J Dev Biol. 2018; 62(1-2-3):97-107. DOI: 10.1387/ijdb.170321ja. View

4.
Davies R, Flint J, Myers S, Mott R . Rapid genotype imputation from sequence without reference panels. Nat Genet. 2016; 48(8):965-969. PMC: 4966640. DOI: 10.1038/ng.3594. View

5.
Howell G, Shindo M, Murray S, Gridley T, Wilson L, Schimenti J . Mutation of a ubiquitously expressed mouse transmembrane protein (Tapt1) causes specific skeletal homeotic transformations. Genetics. 2006; 175(2):699-707. PMC: 1800629. DOI: 10.1534/genetics.106.065177. View