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利用长读长 Oxford Nanopore 测序技术对婆罗门牛的 poll 等位基因进行特征分析。

Characterization of the poll allele in Brahman cattle using long-read Oxford Nanopore sequencing.

机构信息

Centre for Animal Science, Queensland Alliance for Agriculture and Food Innovation, University of Queensland, St Lucia, QLD, Australia.

Neogen Australasia, University of Queensland, Gatton, QLD, Australia.

出版信息

J Anim Sci. 2020 May 1;98(5). doi: 10.1093/jas/skaa127.

Abstract

Brahman cattle (Bos indicus) are well adapted to thrive in tropical environments. Since their introduction to Australia in 1933, Brahman's ability to grow and reproduce on marginal lands has proven their value in the tropical beef industry. The poll phenotype, which describes the absence of horns, has become desirable in the cattle industry for animal welfare and handler safety concerns. The poll locus has been mapped to chromosome one. Four alleles, each a copy number variant, have been reported across this locus in B. indicus and Bos taurus. However, the causative mutation in Brahman cattle has not been fully characterized. Oxford Nanopore Technologies' minION sequencer was used to sequence four homozygous poll (PcPc), four homozygous horned (pp), and three heterozygous (Pcp) Brahmans to characterize the poll allele in Brahman cattle. A total of 98 Gb were sequenced and an average coverage of 3.33X was achieved. Read N50 scores ranged from 9.9 to 19 kb. Examination of the mapped reads across the poll locus revealed insertions approximately 200 bp in length in the poll animals that were absent in the horned animals. These results are consistent with the Celtic poll allele, a 212-bp duplication that replaces 10 bp. This provides direct evidence that the Celtic poll allele is segregating in the Australian Brahman population.

摘要

婆罗门牛(Bos indicus)非常适应在热带环境中生长和繁殖。自 1933 年引入澳大利亚以来,婆罗门牛在边缘土地上生长和繁殖的能力证明了它们在热带牛肉行业的价值。无角表型描述了没有角的特征,这在牛业中由于动物福利和处理者安全的考虑变得很受欢迎。该无角基因座已被定位到染色体 1 上。在 B. indicus 和 Bos taurus 中,该基因座已报道了四个等位基因,每个等位基因都是拷贝数变异。然而,婆罗门牛中的致突变尚未完全确定。牛津纳米孔技术的 MinION 测序仪用于对四个纯合无角(PcPc)、四个纯合有角(pp)和三个杂合(Pcp)婆罗门牛进行测序,以对婆罗门牛中的无角等位基因进行特征分析。总共测序了 98GB,平均覆盖率达到 3.33X。读长 N50 分数范围从 9.9 到 19kb。对无角基因座上的映射读取进行检查,发现无角动物中不存在的无角动物的插入约 200bp 长。这些结果与凯尔特无角等位基因一致,该等位基因是 212bp 的重复,取代了 10bp。这提供了直接证据表明,凯尔特无角等位基因在澳大利亚婆罗门牛群体中分离。

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