Journal
ANIMAL GENETICS
Volume 51, Issue 6, Pages 945-949Publisher
WILEY
DOI: 10.1111/age.12998
Keywords
genetic disorder; impaired male fertility; sperm maturation defect; sterility
Funding
- SUISAG
- Migros
- ETH Zurich Foundation
- Finnish Veterinary Research Foundation
- Ministry of Agriculture and Forestry of Finland
- Suomen Sianjalostuksen Saatio
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A recessive sperm defect of Yorkshire boars was detected more than a decade ago. Affected boars produce ejaculates that contain spermatozoa with defective acrosomes, resulting in low fertility. The acrosome defect was mapped to porcine chromosome 15 but the causal mutation has not been identified. We re-analyzed microarray-derived genotypes of affected boars and confirmed that the acrosome defect maps to a 12.24 Mb segment of porcine chromosome 15. To detect the mutation causing defective acrosomes, we sequenced the genomes of two affected and three unaffected boars to an average coverage of 11-fold. Read depth analysis revealed a 55 kb deletion that is associated with the acrosome defect. The deletion encompasses theBOLLgene encoding the boule homolog, an RNA binding protein which is an evolutionarily conserved member of theDAZ(Deleted in AZoospermia) gene family. Lack ofBOLLexpression causes spermatogenic arrest and sperm maturation failure in many species. Boars that carry the deletion in the homozygous state produce sperm but their acrosomes are defective, suggesting that lack of porcine BOLL compromises acrosome formation. Our findings warrant further research to investigate the role ofBOLLduring spermatogenesis and sperm maturation in pigs.
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