已知蚊子(双翅目:库蚊科)有丝分裂基因组的系统发育关系

IF 1.1 4区 生物学 Q4 GENETICS & HEREDITY Mitochondrial Dna Part a Pub Date : 2018-01-02 DOI:10.1080/24701394.2016.1233533
Hong-liang Chu, Chun-Xiao Li, Xiao-xia Guo, Heng-duan Zhang, Peng Luo, Zhonghua Wu, Gang Wang, T. Zhao
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引用次数: 14

摘要

摘要从GenBank中收集已知蚊子有丝分裂基因组,共34种,隶属于5属,评估线粒体DNA全基因组和部分线粒体COI基因变异的实用性和有效性,重建蚊子的系统发育。基于简约、最大似然和贝叶斯(BI)方法重建了系统发育树。结果表明:(1)有丝分裂基因组和COI基因均支持以下类群的单一性:新吻按蚊亚属、蜂窝按蚊亚属、阿尔比特按蚊复合体、冈比亚按蚊复合体和点状按蚊群;(2)伊蚊属与警戒伊蚊属不是单系的;(3)表观按蚊与冈比亚按蚊复合体、大毒按蚊复合体和点状按蚊群亲缘关系较近;(4)有丝分裂基因组重建的系统发育树的贝叶斯后验概率(BPP)高于COI树。结果表明,利用有丝分裂基因组重建的系统发育关系与基于形态学数据的系统发育关系更为相似。
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The phylogenetic relationships of known mosquito (Diptera: Culicidae) mitogenomes
Abstract The known mosquito mitogenomes, containing a total of 34 species, which belong to five genera, were collected from GenBank, and the practicality and effectiveness of the variation in the complete mitochondrial DNA genome and portions of mitochondrial COI gene were assessed to reconstruct the phylogeny of mosquitoes. Phylogenetic trees were reconstructed on the basis of parsimony, maximum likelihood, and Bayesian (BI) methods. It is concluded that: (1) Both mitogenomes and COI gene support the monophly of following taxa: Subgenus Nyssorhynchus, Subgenus Cellia, Anopheles albitarsis complex, Anopheles gambiae complex, and Anopheles punctulatus group; (2) Genus Aedes is not monophyletic relative to Ochlerotatus vigilax; (3) The mitogenome results indicate a close relationship between Anopheles epiroticus and Anopheles gambiae complex, Anopheles dirus complex and Anopheles punctulatus group, respectively; (4) The Bayesian posterior probability (BPP) within phylogenetic tree reconstructed by mitogenomes is higher than COI tree. The results show that phylogenetic relationships reconstructed using the mitogenomes were more similar to those based on morphological data.
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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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