巴尔干短毛牛——欧洲最早驯养的牛

IF 1.1 4区 生物学 Q4 GENETICS & HEREDITY Mitochondrial Dna Part a Pub Date : 2018-01-02 DOI:10.1080/24701394.2016.1238901
P. Hristov, D. Sirakova, I. Mitkov, N. Spassov, G. Radoslavov
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引用次数: 3

摘要

摘要本研究旨在比较巴尔干新石器/铜石器时代牛与现代短刺红紫荆牛(Busha)的线粒体多样性,为欧洲牛驯化提供新的视角。结果表明,古代和现代样品均属于t大单倍群。在28个序列(8个古代序列和20个现代序列)中,T1和T2单倍群约占3.6% (1/28;1/28)。T3单倍群发生率最高,为57%(16/28)。基于16057A和16133C的snp,提出了新的T6单倍群。这个单倍群占古代保加利亚短毛牛种群的75%,占现代保加利亚短毛牛种群的20%。GenBank数据库的调查没有发现类似的主题,除了最近的塞尔维亚布沙牛。总体而言,这些结果表明:(1)新命名的T6单倍群是巴尔干特有的;(ii) T6单倍群在今天的保加利亚rhodopean牛中存活;巴尔干短链牛是欧洲最古老的牛品种。
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Balkan brachicerous cattle – the first domesticated cattle in Europe
Abstract The present study aimed to compare mitochondrial diversity among Balkan Neolithic/Chalcolithic cattle and present day Shorthorn Rhodopean cattle (Busha) to throw a new insight into European cattle domestication. The results showed that both ancient- and present-day samples belonged to the macrohaplogroup T. From the 28 sequences (8 ancient and 20 modern), the T1 and T2 haplogroup represent about 3.6% (1/28; 1/28). The T3 haplogroup was with the highest frequency – 57% (16/28). Based on the SNPs on 16057A and 16133C, the new T6 haplogroup was proposed. This haplogroup represents 75% from the ancient and 20% from the present day Bulgarian brachicerous cattle population. The survey in GenBank data base did not find a similar motif, except for the recent Serbian Busha cattle. Overall, these results showed that: (i) The newly named T6 haplogroup is Balkan specific; (ii) The T6 haplogroup survives in present day Bulgarian rhodopean cattle; (iii) The Balkan brachicerous cattle is the oldest European cattle breed.
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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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