Association of low race performance with mtDNA haplogroup L3b of Australian thoroughbred horses

IF 1.1 4区 生物学 Q4 GENETICS & HEREDITY
Xiang-rong Lin, Hong-Xiang Zheng, A. Davie, Shi Zhou, L. Wen, Jun Meng, Yong Zhang, QI · Aladaer, B. Liu, Wujun Liu, Xinkui Yao
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引用次数: 5

Abstract

Abstract Mitochondrial DNA (mtDNA) encodes the genes for respiratory chain sub-units that determine the efficiency of oxidative phosphorylation in mitochondria. The aim of this study was to determine if there were any haplogroups and variants in mtDNA that could be associated with athletic performance of Thoroughbred horses. The whole mitochondrial genomes of 53 maternally unrelated Australian Thoroughbred horses were sequenced and an association study was performed with the competition histories of 1123 horses within their maternal lineages. A horse mtDNA phylogenetic tree was constructed based on a total of 195 sequences (including 142 from previous reports). The association analysis showed that the sample groups with poor racing performance history were enriched in haplogroup L3b (p = .0003) and its sub-haplogroup L3b1a (p = .0007), while those that had elite performance appeared to be not significantly associated with haplogroups G2 and L3a1a1a (p > .05). Haplogroup L3b and L3b1a bear two and five specific variants of which variant T1458C (site 345 in 16s rRNA) is the only potential functional variant. Furthermore, secondary reconstruction of 16s RNA showed considerable differences between two types of 16s RNA molecules (with and without T1458C), indicating a potential functional effect. The results suggested that haplogroup L3b, could have a negative association with elite performance. The T1458C mutation harboured in haplogroup L3b could have a functional effect that is related to poor athletic performance.
澳大利亚纯种马mtDNA单倍群L3b与低比赛表现的关系
线粒体DNA (mtDNA)编码呼吸链亚基的基因,这些亚基决定线粒体氧化磷酸化的效率。本研究的目的是确定是否有任何单倍群和变异的mtDNA可能与纯种马的运动表现有关。对53匹母系无亲缘关系的澳大利亚纯种马的全线粒体基因组进行了测序,并与母系内1123匹马的竞争史进行了关联研究。基于195个序列(包括先前报道的142个序列)构建了马mtDNA系统发育树。关联分析表明,成绩较差的样本群体在单倍群L3b (p = 0.0003)及其亚单倍群L3b1a (p = 0.0007)中富集,而成绩优异的样本群体与单倍群G2和L3a1a1a的相关性不显著(p = 0.05)。单倍群L3b和L3b1a分别有2个和5个特定的变体,其中变体T1458C (16s rRNA中的345位点)是唯一潜在的功能变体。此外,16s RNA的二次重建显示两种类型的16s RNA分子(含T1458C和不含T1458C)之间存在相当大的差异,表明可能存在功能作用。结果表明,单倍群L3b可能与精英表现呈负相关。L3b单倍群中的T1458C突变可能具有与运动表现差有关的功能影响。
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来源期刊
Mitochondrial Dna Part a
Mitochondrial Dna Part a Biochemistry, Genetics and Molecular Biology-Genetics
CiteScore
3.00
自引率
0.00%
发文量
6
期刊介绍: Mitochondrial DNA Part A publishes original high-quality manuscripts on physical, chemical, and biochemical aspects of mtDNA and proteins involved in mtDNA metabolism, and/or interactions. Manuscripts on cytosolic and extracellular mtDNA, and on dysfunction caused by alterations in mtDNA integrity as well as methodological papers detailing novel approaches for mtDNA manipulation in vitro and in vivo are welcome. Descriptive papers on DNA sequences from mitochondrial genomes, and also analytical papers in the areas of population genetics, phylogenetics and human evolution that use mitochondrial DNA as a source of evidence for studies will be considered for publication. The Journal also considers manuscripts that examine population genetic and systematic theory that specifically address the use of mitochondrial DNA sequences, as well as papers that discuss the utility of mitochondrial DNA information in medical studies and in human evolutionary biology.
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