Jacinto Joana G P, Letko Anna, Häfliger Irene M, Akyürek Eylem Emek, Sacchetto Roberta, Gentile Arcangelo, Drögemüller Cord
Institute of Genetics, Vetsuisse Faculty, University of Bern, Bern, 3012, Switzerland.
Clinic for Ruminants, Vetsuisse Faculty, University of Bern, Bern, 3012, Switzerland.
Sci Rep. 2024 Dec 28;14(1):31188. doi: 10.1038/s41598-024-82446-z.
Bovine spastic syndrome (SS) is a progressive, adult-onset neuromuscular disorder (NMD). SS is inherited but the mode of inheritance is unclear. The aim of this study was to characterize the phenotype and to identify a possible genetic cause of SS by whole-genome sequencing (WGS) and focusing on protein-changing variants. Seven affected unrelated Holstein cattle of both sexes were referred for SS at a mean age of 5.3 years (S.D.±1.1) showing intermittent spasm of the skeletal muscles of the pelvic girdle. Assuming monogenic recessive inheritance, analysis of the WGS data did not reveal any private variants common to all cases. Searching for homozygous rare variants considering each case individually, allowed the identification of a rare recessive likely pathogenic missense variant in TOR3A for one case with an allele frequency of 1.69% in a global Holstein population. In the remaining six SS cases, we identified seven potentially dominant de novo mutations or inherited alleles as private heterozygous, mostly missense, variants of uncertain significance involving seven different NMD candidate genes: MPEG1, LHX8, WHAMM, NGRN, TTN, ATP1A1, PCDH1. All eight candidate causal variants identified were predicted to be deleterious. This study describes for the first time WGS findings in confirmed cases of bovine SS and provides evidence for a heterogeneous genetic cause of SS in cattle.
牛痉挛综合征(SS)是一种进行性、成年起病的神经肌肉疾病(NMD)。SS是遗传性的,但遗传方式尚不清楚。本研究的目的是通过全基因组测序(WGS)并聚焦于蛋白改变变体来表征该疾病的表型并确定SS可能的遗传原因。七头患有SS的无亲缘关系的荷斯坦牛(雌雄均有)被转诊,平均年龄为5.3岁(标准差±1.1),表现为骨盆带骨骼肌间歇性痉挛。假设为单基因隐性遗传,对WGS数据的分析未发现所有病例共有的任何私有变体。单独考虑每个病例来寻找纯合罕见变体,使得在一个病例中鉴定出TOR3A基因中一个罕见的隐性可能致病错义变体,在全球荷斯坦牛群体中的等位基因频率为1.69%。在其余六个SS病例中,我们鉴定出七个潜在的显性新生突变或作为私有杂合子遗传的等位基因,大多为错义变体,涉及七个不同的NMD候选基因:MPEG1、LHX8、WHAMM、NGRN、TTN、ATP1A1、PCDH1。所鉴定出的所有八个候选致病变体预计都是有害的。本研究首次描述了确诊的牛SS病例的WGS结果,并为牛SS的异质性遗传原因提供了证据。