Genomic Sequencing to Detect Cross-Breeding Quality in Dogs: An Example Studying Disorders in Sexual Development

• Published in: International journal of molecular sciences Vol. 25; no. 19; p. 10763
• Main Authors: de Gennaro, Luciana, Burgio, Matteo, Lacalandra, Giovanni Michele, Petronella, Francesco, L'Abbate, Alberto, Ravasini, Francesco, Trombetta, Beniamino, Rizzo, Annalisa, Ventura, Mario, Cicirelli, Vincenzo
• Format: Journal Article
• Language: English
• Published: Switzerland MDPI AG 01.10.2024; MDPI
• Subjects: Animals; breed; Breeding; Causes of; Disorders of Sex Development - genetics; Disorders of Sex Development - veterinary; DNA sequencing; Dog breeding; Dog Diseases - genetics; Dogs; Female; French Bulldog; Genes; Genetic aspects; Genome; Genomes; genomics; Genomics - methods; High-Throughput Nucleotide Sequencing; Male; Methods; Mitochondrial DNA; Mutation; Nucleotide sequencing; Penis; Phenotype; Polymorphism, Single Nucleotide; Pseudohermaphroditism; run of homozygosity; Sex chromosomes; Sex differentiation disorders; X chromosomes; Italy; dogs; genomics; French Bulldog; run of homozygosity; breed
• ISSN: 1422-0067; 1661-6596; 1422-0067
• DOI: 10.3390/ijms251910763

Disorders of sexual development (DSDs) in dogs, similar to humans, arise from genetic mutations, gonadal differentiation, or phenotypic sex development. The French Bulldog, a breed that has seen a surge in popularity and demand, has also shown a marked increase in DSD incidence. This study aims to characterize the genetic underpinnings of DSDs in a French Bulldog named , exhibiting ambiguous genitalia and internal sexual anatomy, and to explore the impact of breeding practices on genetic diversity within the breed. We utilized a comprehensive approach combining conventional cytogenetics, molecular techniques, and deep sequencing to investigate the genetic profile of . The sequence data were compared to three other male French Bulldogs' genome sequences with typical reproductive anatomy, including 's father and the canine reference genome (CanFam6). We found a Robertsonian fusion involving chromosome 23 previously reported in dogs as a causative mutation responsible for sex reversal syndrome. Our findings revealed a 22% mosaicism (78,XX/77,XX), the absence of the sex-determining region ( ) gene, and the presence of 43 unique Single Nucleotide Variants (SNVs) not inherited from the father. Notably, the run of homozygosity (ROH) analysis showed has a higher number of homozygous segments compared to other Bulldogs, with a total length of these fragments 50% greater than the average, strongly suggesting this dog is the product of the mating between siblings. Although no direct causative genes for the DSD phenotype were identified, four candidate loci warrant further investigation. Our study highlighted the need for a better annotated and curated reference dog genome to define genes causative of any specific phenotype, suggests a potential genetic basis for the DSD phenotype in dogs, and underscores the consequences of uncontrolled breeding practices in French Bulldogs. These findings highlight the importance of implementing strategic genetic management to preserve genetic health and diversity in canine populations.