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Weighted Single-Step Genome-Wide Association Study Uncovers Known and Novel Candidate Genomic Regions for Milk Production Traits and Somatic Cell Score in Valle del Belice Dairy Sheep
oleh: Hossein Mohammadi, Amir Hossein Khaltabadi Farahani, Mohammad Hossein Moradi, Salvatore Mastrangelo, Rosalia Di Gerlando, Maria Teresa Sardina, Maria Luisa Scatassa, Baldassare Portolano, Marco Tolone
Format: | Article |
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Diterbitkan: | MDPI AG 2022-04-01 |
Deskripsi
The objective of this study was to uncover genomic regions explaining a substantial proportion of the genetic variance in milk production traits and somatic cell score in a Valle del Belice dairy sheep. Weighted single-step genome-wide association studies (WssGWAS) were conducted for milk yield (MY), fat yield (FY), fat percentage (FAT%), protein yield (PY), protein percentage (PROT%), and somatic cell score (SCS). In addition, our aim was also to identify candidate genes within genomic regions that explained the highest proportions of genetic variance. Overall, the full pedigree consists of 5534 animals, of which 1813 ewes had milk data (15,008 records), and 481 ewes were genotyped with a 50 K single nucleotide polymorphism (SNP) array. The effects of markers and the genomic estimated breeding values (GEBV) of the animals were obtained by five iterations of WssGBLUP. We considered the top 10 genomic regions in terms of their explained genomic variants as candidate window regions for each trait. The results showed that top ranked genomic windows (1 Mb windows) explained 3.49, 4.04, 5.37, 4.09, 3.80, and 5.24% of the genetic variances for MY, FY, FAT%, PY, PROT%, and total SCS, respectively. Among the candidate genes found, some known associations were confirmed, while several novel candidate genes were also revealed, including <i>PPARGC1A</i>, <i>LYPLA1</i>, <i>LEP</i>, and <i>MYH9</i> for MY; <i>CACNA1C, PTPN1, ROBO2, CHRM3,</i> and <i>ERCC6</i> for FY and FAT%; <i>PCSK5</i> and <i>ANGPT1</i> for PY and PROT%; and <i>IL26</i>, <i>IFNG</i>, <i>PEX26</i>, <i>NEGR1</i>, <i>LAP3</i>, and <i>MED28</i> for SCS. These findings increase our understanding of the genetic architecture of six examined traits and provide guidance for subsequent genetic improvement through genome selection.