斑点粪便Scatophagus argus (Teleostei, Scatophagidae)线粒体全基因组研究。

Mitochondrial Dna Pub Date : 2015-04-01 Epub Date: 2013-09-09 DOI:10.3109/19401736.2013.830295

Jianhua Chen, Yinglei Li, Maoxian He, Binlun Yan, Xueping Meng

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引用次数: 1

摘要

采用长扩增聚合酶链反应(LA-PCR)测定了斑点粪便Scatophagus argus的线粒体全序列。该序列全长16778 bp，包含13个蛋白质编码基因、2个核糖体RNA基因、22个转移RNA基因和1个控制区。h链碱基组成分别为27.23% (A)、27.54% (T)、16.22% (G)和28.81% (C)， AT含量为55.08%。argus的基因排列与其他鱼类相同。除ND6和8个tRNA基因外，所有基因都编码在重链上。本文介绍的argus的线粒体基因组将有助于解决Scatophagidae家族和Perciformes之间的系统发育关系。

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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Complete mitochondrial genome of the spotted scat Scatophagus argus (Teleostei, Scatophagidae).

The complete mitochondrial sequence of the spotted scat Scatophagus argus has been determined using long amplification polymerase chain reaction (LA-PCR). The total length of sequence is 16,778 bp, and includes 13 protein-coding genes, 2 ribosomal RNA genes, 22 transfer RNA genes and 1 control region. The base composition of H-strand is 27.23% (A), 27.54% (T), 16.22% (G) and 28.81% (C), with an AT content of 55.08%. The arrangement of genes in S. argus is identical to that of other fish species. All genes are encoded on the heavy strand with the exception of ND6 and eight tRNA genes. The mitochondrial genome of S. argus presented here will contribute to resolve phylogenetic relationships within the family Scatophagidae and the Perciformes.

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来源期刊

Mitochondrial Dna 生物-遗传学

自引率

0.00%

发文量

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.