欧洲褐兔(Lepus europaeus)的有丝分裂基因组分析提出了不同谱系之间的遗传和功能分化

IF 1.1 4区 生物学 Q4 GENETICS & HEREDITY Mitochondrial Dna Part a Pub Date : 2018-04-01 DOI:10.1080/24701394.2016.1278540
T. Giannoulis, C. Stamatis, Andreas Tsipourlianos, Z. Mamuris
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引用次数: 14

摘要

摘要欧洲褐兔是一种分布于欧洲至小亚细亚的小型狩猎物种,具有重要的经济特征。使用线粒体DNA标记的群体遗传学研究揭示了两个主要的系统地理谱系的存在,欧洲人和安纳托利亚人。欧洲谱系进一步划分为欧洲型哈尔泊群和东南欧型哈尔泊群,而安纳托利亚仅由安纳托利亚/中东型哈尔泊群组成。这三个单倍群的地理分布都是离散的,在希腊东北部和保加利亚形成了一个重叠的区域,形成了一个接触区。尽管存在接触区,但在安纳托利亚从未检测到欧洲单倍型,反之亦然,这表明存在遗传障碍,导致了这种现象。在这项研究中,我们分析了来自两个谱系的标本的整个线粒体基因组,旨在检测mtDNA编码的氧化磷酸化复合物的遗传和功能分化,这些氧化磷酸化复合物可能逐渐导致谱系的生殖隔离。
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Mitogenomic analysis in European brown hare (Lepus europaeus) proposes genetic and functional differentiation between the distinct lineages
Abstract European brown hare is a small game species spreading across Europe to Asia Minor, with important economic traits. Population genetics studies using mitochondrial DNA markers have revealed the existence of two major phylogeographic lineages, the European and the Anatolian. European lineage is further divided in the European type halpogroup and south-eastern European type halpogroup, while Anatolian consists only by the Anatolian/Middle Eastern type halpogroup. All three haplogroups show a discrete geographical distribution, with an overlapping zone forming in North-East Greece and Bulgaria, forming a contact zone. Despite the existence of a contact zone, European haplotype was never detected in Anatolia and vice versa, proposing the presence of genetic barriers responsible for this phenomenon. In this study, we analyzed the whole mitochondrial genomes of specimens originating from both lineages, aiming to detect the genetic and functional differentiation of the oxidative phosphorylation complexes that are encoded by mtDNA that could lead gradually to the reproductive isolation of the lineages.
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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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