Prevalence of sex-chromosome aneuploidy estimated using SNP genotype intensity information in a large population of juvenile dairy and beef cattle

IF 1.9 3区 农林科学 Q2 AGRICULTURE, DAIRY & ANIMAL SCIENCE Journal of Animal Breeding and Genetics Pub Date : 2024-03-29 DOI:10.1111/jbg.12866
Cliona A. Ryan, Deirdre C. Purfield, Daragh Matthews, Carla Canedo-Ribeiro, Ainhoa Valldecabres, Donagh P. Berry
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Abstract

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.

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利用 SNP 基因型强度信息估算大量幼年奶牛和肉牛的性染色体非整倍体流行率。
非整倍体是一种遗传病,其特征是一条或多条染色体缺失或增殖。影响性染色体的非整倍体可导致外部表型正常的牛不育。及早发现性染色体非整倍体牛对于最大限度地降低饲养不育牛和徒劳的育种尝试所带来的成本非常重要。由于大多数家畜育种项目都会使用单核苷酸多态性(SNP)阵列对育种群体进行常规基因分型,因此本研究旨在评估将非整倍体筛选工具整合到处理高密度 SNP 基因分型数据的现有管道中的可行性。研究的另一个目的是利用现有的基因型强度数据估算146,431头幼牛群体中性染色体非整倍体的发生率。研究中使用了三种基因型强度统计量:对数比(LRR)、R 值(X 和 Y SNP 探针强度之和)和 B 等位基因频率(BAF)测量值。在由 124 958 人组成的女性验证人群中,XO 的患病率估计为 0.0048%,XXX 为 0.0350%,XXY 为 0.0004%。男性验证人群中的 XXY 患病率为 0.0870%(即 20,670 名男性中有 18 名 XXY 患者)。细胞遗传学检测用于验证 2 名仍在世的 XXX 女性。所提出的方法可以很容易地集成到现有的基因组管道中,成为一种高效、大规模的非整倍体筛查工具。采用这种方法可以及早发现患有性染色体非整倍体的不育动物。
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来源期刊
Journal of Animal Breeding and Genetics
Journal of Animal Breeding and Genetics 农林科学-奶制品与动物科学
CiteScore
5.20
自引率
3.80%
发文量
58
审稿时长
12-24 weeks
期刊介绍: The Journal of Animal Breeding and Genetics publishes original articles by international scientists on genomic selection, and any other topic related to breeding programmes, selection, quantitative genetic, genomics, diversity and evolution of domestic animals. Researchers, teachers, and the animal breeding industry will find the reports of interest. Book reviews appear in many issues.
期刊最新文献
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