Population Genomics Group, Department of Veterinary Sciences, LMU Munich, Veterinärstr. 13, 80539, Munich, Germany.
Laboratory for Functional Genome Analysis, Gene Center Munich, LMU Munich, Feodor-Lynen-Str. 25, 81377, Munich, Germany.
Genet Sel Evol. 2018 Jul 6;50(1):36. doi: 10.1186/s12711-018-0407-9.
It has been known for almost a century that the belted phenotype in cattle follows a pattern of dominant inheritance. In 2009, the approximate position of the belt locus in Brown Swiss cattle was mapped to a 922-kb interval on bovine chromosome 3 and, subsequently, assigned to a 336-kb haplotype block based on an animal set that included, Brown Swiss, Dutch Belted (Lakenvelder) and Belted Galloway individuals. A possible candidate gene in this region i.e. HES6 was investigated but the causal mutation remains unknown. Thus, to elucidate the causal mutation of this prominent coat color phenotype, we decided to remap the belted phenotype in an independent animal set of several European bovine breeds, i.e. Gurtenvieh (belted Brown Swiss), Dutch Belted and Belted Galloway and to systematically scan the candidate region. We also checked the presence of the detected causal mutation in the genome of belted individuals from a Siberian cattle breed.
A combined linkage disequilibrium and linkage analysis based on 110 belted and non-belted animals identified a candidate interval of 2.5 Mb. Manual inspection of the haplotypes in this region identified four candidate haplotypes that consisted of five to eight consecutive SNPs. One of these haplotypes overlapped with the initial 922-kb interval, whereas two were positioned proximal and one was positioned distal to this region. Next-generation sequencing of one heterozygous and two homozygous belted animals identified only one private belted candidate allele, i.e. a multiplication event that is located between 118,608,000 and 118,614,000 bp. Targeted locus amplification and quantitative real-time PCR confirmed an increase in copy number of this region in the genomes of both European (Belted Galloway, Dutch Belted and Gurtenvieh) and Siberian (Yakutian cattle) breeds. Finally, using nanopore sequencing, the exact breakpoints were determined at 118,608,362 and 118,614,132 bp. The closest gene to the candidate causal mutation (16 kb distal) is TWIST2.
Based on our findings and those of a previously published study that identified the same multiplication event, a quadruplication on bovine chromosome 3 between positions 118,608,362 and 118,614,132 bp is the most likely candidate causal mutation for the belted phenotype in cattle.
近一个世纪以来,人们已经知道牛的带花纹表型遵循显性遗传模式。2009 年,棕色瑞士牛的带花纹基因座的大致位置被定位在牛 3 号染色体上的 922-kb 区间,并随后根据包括棕色瑞士牛、荷兰带花纹牛(Lakenvelder)和带花纹盖洛威牛在内的动物集合,将其分配到一个 336-kb 的单倍型块中。在该区域的一个可能的候选基因 HES6 进行了研究,但因果突变仍然未知。因此,为了阐明这种明显的毛色表型的因果突变,我们决定在几个欧洲牛品种的独立动物集合中重新映射带花纹表型,即 Gurtenvieh(带花纹棕色瑞士牛)、荷兰带花纹牛和带花纹盖洛威牛,并系统地扫描候选区域。我们还检查了来自西伯利亚牛品种的带花纹个体的基因组中是否存在检测到的因果突变。
基于 110 头带花纹和非带花纹动物的连锁不平衡和连锁分析,确定了一个 2.5 Mb 的候选区间。对该区域的单倍型进行手动检查,确定了四个候选单倍型,它们由 5 到 8 个连续的 SNP 组成。其中一个单倍型与最初的 922-kb 区间重叠,而两个位于该区域的近端,一个位于该区域的远端。对一个杂合和两个纯合带花纹动物的下一代测序只确定了一个私有带花纹候选等位基因,即位于 118,608,000 到 118,614,000 bp 之间的倍增事件。靶向基因座扩增和定量实时 PCR 证实了该区域在欧洲(带花纹盖洛威牛、荷兰带花纹牛和 Gurtenvieh)和西伯利亚(雅库特牛)品种的基因组中的拷贝数增加。最后,使用纳米孔测序确定了确切的断点,分别为 118,608,362 和 118,614,132 bp。最接近候选因果突变(16 kb 远端)的基因是 TWIST2。
基于我们的发现和之前发表的一项研究的结果,该研究确定了相同的倍增事件,牛 3 号染色体上 118,608,362 到 118,614,132 bp 之间的四重复是牛带花纹表型最有可能的候选因果突变。