Genomic sequencing to detect cross-breeding quality in dogs: an example studying disorders in sexual development

bioRxiv Pub Date : 2024-08-08 DOI:10.1101/2024.08.07.606952
Luciana de Gennaro, Matteo Burgio, G. Lacalandra, Francesco Petronella, Alberto L’Abbate, Francesco Ravasini, B. Trombetta, Annalisa Rizzo, Mario Ventura, Vincenzo Cicirelli
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Abstract

Background Disorders of Sexual Development (DSD) in dogs, similar to humans, arise from irregularities in genetic determinants, 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 DSD in a French Bulldog named Brutus, exhibiting ambiguous genitalia and internal sexual anatomy, and to explore the impact of breeding practices on genetic diversity within the breed. Methods We utilized a comprehensive approach combining conventional cytogenetics, molecular techniques, and deep sequencing to investigate the genetic profile of Brutus. The sequence data were compared to three other male French Bulldogs genome sequences with typical reproductive anatomy, including Brutus’s father, and the canine reference genome (CanFam6). Findings Our findings revealed a 22% mosaicism (78, XX/77, XX), the absence of the SRY gene, and the presence of 43 unique Single Nucleotide Variants (SNVs) not inherited from the father. Notably, the Run of Homozygosity (ROH) analysis showed Brutus has a significantly 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. While no direct causative genes for the DSD phenotype were identified four candidate loci warranting further investigation were highlighted. Conclusions 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.
基因组测序检测狗的杂交质量:研究性发育障碍的一个实例
背景 狗的性发育障碍(DSD)与人类类似,都是由遗传决定因素、性腺分化或表型性发育不正常引起的。法国斗牛犬作为一种受欢迎程度和需求量激增的犬种,DSD发病率也明显增加。本研究旨在描述一只名为 "Brutus "的法国斗牛犬DSD的遗传基础,该犬的生殖器和内部性解剖结构模糊不清,本研究还旨在探讨育种方法对该犬种遗传多样性的影响。方法 我们采用传统细胞遗传学、分子技术和深度测序相结合的综合方法来研究 Brutus 的遗传特征。我们将序列数据与其他三个具有典型生殖解剖结构的雄性法国斗牛犬基因组序列(包括 Brutus 的父亲)以及犬类参考基因组 (CanFam6) 进行了比较。研究结果 我们的研究结果表明,Brutus 的基因组嵌合率为 22%(78, XX/77, XX),缺少 SRY 基因,而且存在 43 个独特的单核苷酸变异 (SNV),这些变异不是从父亲那里遗传来的。值得注意的是,同源性分析(ROH)显示,与其他斗牛犬相比,Brutus 的同源性片段数量明显较多,这些片段的总长度比平均值高出 50%,这有力地证明了该犬是兄弟姐妹间交配的产物。虽然没有发现 DSD 表型的直接致病基因,但强调了四个值得进一步研究的候选基因位点。结论 我们的研究强调了对参考犬基因组进行更好的注释和编辑以确定任何特定表型的致病基因的必要性,提出了犬 DSD 表型的潜在遗传基础,并强调了法国斗牛犬无节制繁殖的后果。这些发现强调了实施战略性遗传管理以保护犬类遗传健康和多样性的重要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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