Classification and phylogeny of sika deer (Cervus nippon) subspecies based on the mitochondrial control region DNA sequence using an extended sample set.

Mitochondrial Dna Pub Date : 2015-06-01 Epub Date: 2013-09-25 DOI:10.3109/19401736.2013.836509
Hengxing Ba, Fuhe Yang, Xiumei Xing, Chunyi Li
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引用次数: 8

Abstract

To further refine the classification and phylogeny of sika deer subspecies, the well-annotated sequences of the complete mitochondrial DNA (mtDNA) control region of 13 sika deer subspecies from GenBank were downloaded, aligned and analyzed in this study. By reconstructing the phylogenetic tree with an extended sample set, the results revealed a split between Northern and Southern Mainland Asia/Taiwan lineages, and moreover, two subspecies, C.n.mantchuricus and C.n.hortulorum, were existed in Northern Mainland Asia. Unexpectedly, Dybowskii's sika deer that was thought to originate from Northern Mainland Asia joins the Southern Mainland Asia/Taiwan lineage. The genetic divergences were ranged from 2.1% to 4.7% between Dybowskii's sika deer and all the other established subspecies at the mtDNA sequence level, which suggests that the maternal lineage of uncertain sika subspecies in Europe had been maintained until today. This study also provides a better understanding for the classification, phylogeny and phylogeographic history of sika deer subspecies.

基于线粒体控制区DNA序列的梅花鹿亚种分类及系统发育研究。
为了进一步完善梅花鹿亚种的分类和系统发育,本研究从GenBank中下载了13个梅花鹿亚种的全线粒体DNA (mtDNA)控制区序列,并对其进行了比对和分析。通过扩展样本集的系统发育树重建,发现亚洲大陆北部/台湾地区存在北缘和南缘的分离,并且在亚洲大陆北部地区存在两个亚种,即C.n.mantchuricus和C.n.hortulorum。出乎意料的是,被认为起源于亚洲北部大陆的戴博斯基梅花鹿加入了亚洲南部大陆/台湾的血统。在mtDNA序列水平上,戴博斯基梅花鹿与所有已确定的梅花鹿亚种之间的遗传差异在2.1% ~ 4.7%之间,这表明欧洲不确定梅花鹿亚种的母系一直保持到今天。该研究还有助于对梅花鹿亚种的分类、系统发育和系统地理历史的认识。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Mitochondrial Dna
Mitochondrial Dna 生物-遗传学
自引率
0.00%
发文量
0
审稿时长
2.4 months
期刊介绍: Previously published under the title DNA Sequence (Vols 1-19.3), Mitochondrial DNA accepts original high-quality reports based on mapping, sequencing and analysis of mitochondrial DNA and RNA. Descriptive papers on DNA sequences from mitochondrial genomes, and also analytical papers in the areas of population genetics, medical genetics, phylogenetics and human evolution that use mitochondrial DNA as a source of evidence for studies will be considered for publication. The editorial board will also consider manuscripts that examine population genetic and systematic theory that specifically address the use of mitochondrial DNA sequences.
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