Suppr超能文献

利用单核苷酸多态性基因型强度芯片信息估计大型幼年奶牛和肉牛群体中常染色体单体和三体的发生率

Prevalence of Autosomal Monosomy and Trisomy Estimated Using Single Nucleotide Polymorphism Genotype Intensity Chip Information in a Large Population of Juvenile Dairy and Beef Cattle.

作者信息

Ryan Cliona A, Purfield Deirdre C, Matthews Daragh, Rathje Claudia, Valldecabres Ainhoa, Berry Donagh P

机构信息

Department of Animal Bioscience, Teagasc, Moorepark, Co. Cork, Ireland.

Department of Biological Science, Munster Technological University, Co. Cork, Ireland.

出版信息

J Anim Breed Genet. 2025 May;142(3):277-286. doi: 10.1111/jbg.12902. Epub 2024 Oct 14.

Abstract

Aneuploidy, a genetic condition characterised by the deletion (monosomy) or duplication (trisomy) of a chromosome, has been extensively studied in humans, particularly in the context of trisomy on chromosome 21, also known as Down syndrome. Research on autosomal aneuploidy in live-born cattle has been limited to case reports, resulting in a lack of prevalence estimates of aneuploidy in cattle. Furthermore, the viability or lethality of aneuploidy on specific autosomes in cattle has not been well documented. The objective of this study was to estimate the prevalence of autosomal aneuploidy in a large population of new-born and juvenile beef and dairy cattle using single nucleotide polymorphism (SNP) chip genotype intensity data. Of the population of 779,138 cattle genotyped when younger than 15 months of age, 139 cattle (i.e., 0.017%) were diagnosed with one case of autosomal trisomy. Trisomy in only 10 different autosomes were detected (BTA 4, 6, 12, 15, 20, 24, 26, 27, 28 and 29) albeit the one case of trisomy detected on Bos taurus autosome (BTA) 4 was in an additional population of 341,927 cattle that were genotyped at > 15 months of age and was therefore excluded from prevalence estimates to minimise bias. The prevalence of trisomy per chromosome was generally inversely related to the length of the chromosome. Although the number of affected individuals was few, there was no evidence of differences in prevalence by breed, inbreeding level or parental age. The parental origin of the detected cases of trisomy was maternal for 92% of the cases. No cases of monosomy were detected despite the large dataset, which included calves genotyped at birth, indicating the potential lethal nature of monosomy in cattle. Cytogenetic testing was used to verify three of the animals with detected autosomal trisomy who were still alive. Eighteen of the 139 animals identified with autosomal trisomy were recorded as being stillborn, resulting in a prevalence of autosomal aneuploidy in live-born cattle of 0.015%. Of the 121 live-born cattle with autosomal trisomy, a total of 68 died on farm at, on average (standard deviation), 6.8 (8.7) months of age. All animals with autosomal trisomy on BTA 6, 12, 15, 20 or 24 were either stillborn or died on farm within 15 days of birth. This study is the first report of trisomy on BTA 4, 6, 15, 20 and 27 in live-born cattle, as well as the first to document fertile cows with trisomy on BTA 4, 27 or 28. Given that genotype intensity SNP data from SNP-chips are readily available, identifying animals affected with autosomal aneuploidy as well as quantifying and monitoring the incidence can be easily undertaken.

摘要

非整倍体是一种以染色体缺失(单体型)或重复(三体型)为特征的遗传状况,在人类中已得到广泛研究,尤其是在21号染色体三体的情况下,即唐氏综合征。对新生牛常染色体非整倍体的研究仅限于病例报告,导致缺乏牛非整倍体患病率的估计。此外,牛特定常染色体上非整倍体的生存力或致死性尚未得到充分记录。本研究的目的是利用单核苷酸多态性(SNP)芯片基因型强度数据,估计大量新生和幼年肉牛及奶牛群体中常染色体非整倍体的患病率。在779,138头年龄小于15个月时进行基因分型的牛中,有139头(即0.017%)被诊断为一例常染色体三体。仅在10条不同的常染色体上检测到三体(牛染色体4、6、12、15、20、24、26、27、28和29),尽管在牛染色体(BTA)4上检测到的一例三体出现在另一群体的341,927头牛中,这些牛在15个月龄以上进行了基因分型,因此为尽量减少偏差,该例被排除在患病率估计之外。每条染色体的三体患病率通常与染色体长度呈负相关。尽管受影响个体数量较少,但没有证据表明品种、近亲繁殖水平或亲本年龄对患病率有差异。检测到的三体病例中,92%的病例其亲本来源为母本。尽管数据集很大,包括出生时进行基因分型的犊牛,但未检测到单体病例,这表明牛单体具有潜在的致死性。细胞遗传学检测用于验证仍存活的3例检测到常染色体三体的动物。在139头被鉴定为常染色体三体的动物中,有18头被记录为死产,导致新生牛中常染色体非整倍体的患病率为0.015%。在121头患有常染色体三体的新生牛中,共有68头在农场死亡,平均(标准差)死亡年龄为6.8(8.7)个月。所有在BTA 6、12、15、20或24上患有常染色体三体的动物要么死产,要么在出生后15天内死于农场。本研究是首次报道新生牛中BTA 4、6、15、20和27上的三体,也是首次记录BTA 4、27或28上患有三体的可育母牛。鉴于SNP芯片的基因型强度SNP数据很容易获得,识别受常染色体非整倍体影响的动物以及量化和监测发病率都可以很容易地进行。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8144/11975166/8e6d073228ec/JBG-142-277-g002.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验