Teagasc, Moorepark, Fermoy, County Cork, Ireland.
Munster Technological University, Cork, County Cork, Ireland.
J Anim Breed Genet. 2024 Sep;141(5):571-585. doi: 10.1111/jbg.12866. Epub 2024 Mar 29.
Aneuploidy is a genetic condition characterized by the loss or gain of one or more chromosomes. Aneuploidy affecting the sex chromosomes can lead to infertility in otherwise externally phenotypically normal cattle. Early identification of cattle with sex chromosomal aneuploidy is important to minimize the costs associated with rearing infertile cattle and futile breeding attempts. As most livestock breeding programs routinely genotype their breeding populations using single nucleotide polymorphism (SNP) arrays, this study aimed to assess the feasibility of integrating an aneuploidy screening tool into the existing pipelines that handle dense SNP genotype data. A further objective was to estimate the prevalence of sex chromosome aneuploidy in a population of 146,431 juvenile cattle using available genotype intensity data. Three genotype intensity statistics were used: the LogR Ratio (LRR), R-value (the sum of X and Y SNP probe intensities), and B-allele frequency (BAF) measurements. Within the female-verified population of 124,958 individuals, the estimated prevalence rate was 0.0048% for XO, 0.0350% for XXX, and 0.0004% for XXY. The prevalence of XXY in the male-verified population was 0.0870% (i.e., 18 out of 20,670 males). Cytogenetic testing was used to verify 2 of the XXX females who were still alive. The proposed approach can be readily integrated into existing genomic pipelines, serving as an efficient, large-scale screening tool for aneuploidy. Its implementation could enable the early identification of infertile animals with sex-chromosome aneuploidy.
非整倍体是一种遗传病症,其特征是一条或多条染色体的缺失或增加。性染色体非整倍体可导致外观正常的牛不育。早期识别具有性染色体非整倍体的牛对于最小化与饲养不育牛和无效繁殖尝试相关的成本非常重要。由于大多数家畜育种计划通常使用单核苷酸多态性(SNP)阵列对其育种群体进行基因分型,因此本研究旨在评估将非整倍体筛查工具整合到处理密集 SNP 基因型数据的现有管道中的可行性。另一个目标是使用可用的基因型强度数据估算 146431 头青年牛群体中性染色体非整倍体的流行率。使用了三种基因型强度统计数据:对数比(LRR)、R 值(X 和 Y SNP 探针强度的总和)和 B 等位基因频率(BAF)测量值。在经过女性验证的 124958 个人群中,XO 的估计流行率为 0.0048%,XXX 的估计流行率为 0.0350%,XXY 的估计流行率为 0.0004%。在经过男性验证的人群中,XXY 的流行率为 0.0870%(即 20670 头雄性中的 18 头)。使用细胞遗传学测试验证了仍存活的 2 名 XXX 女性。拟议的方法可以很容易地整合到现有的基因组学管道中,作为一种有效的、大规模的非整倍体筛查工具。它的实施可以实现对具有性染色体非整倍体的不育动物的早期识别。