andonta anatina(软体动物:联合科)完整的雌性线粒体基因组:一个新的蛋白质编码基因(forf)的确认。

Mitochondrial Dna Pub Date : 2015-04-01 Epub Date: 2013-09-11 DOI:10.3109/19401736.2013.823176
Marianna Soroka, Artur Burzyński
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引用次数: 18

摘要

淡水贻贝是具有两种不同性别的线粒体基因组的动物之一。我们测序了5个andonta anatina个体的完整雌性线粒体基因组,andonta anatina是一种常见于古北区的双壳类动物。基因组长度可变:15,637-15,653 bp。这种变异几乎完全局限于非编码部分,约占基因组的5%。核苷酸多样性中等,为0.3%。核苷酸组成倾向于AT(66.0%)。所有在动物mtDNA中常见的基因以及统一线粒体基因组的ORF特征都被鉴定出来,使存在的基因总数达到38个。如果这个额外的ORF确实编码了一个蛋白质,它一定是在一个非常宽松的选择下进化的,因为这个基因内的所有替换都是非同义的。基因组的基因顺序和结构与除Gonideini外的所有双壳类雌性线粒体基因组相同。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Complete female mitochondrial genome of Anodonta anatina (Mollusca: Unionidae): confirmation of a novel protein-coding gene (F ORF).

Freshwater mussels are among animals having two different, gender-specific mitochondrial genomes. We sequenced complete female mitochondrial genomes from five individuals of Anodonta anatina, a bivalve species common in palearctic ecozone. The length of the genome was variable: 15,637-15,653 bp. This variation was almost entirely confined to the non-coding parts, which constituted approximately 5% of the genome. Nucleotide diversity was moderate, at 0.3%. Nucleotide composition was typically biased towards AT (66.0%). All genes normally seen in animal mtDNA were identified, as well as the ORF characteristic for unionid mitochondrial genomes, bringing the total number of genes present to 38. If this additional ORF does encode a protein, it must evolve under a very relaxed selection since all substitutions within this gene were non-synonymous. The gene order and structure of the genome were identical to those of all female mitochondrial genomes described in unionid bivalves except the Gonideini.

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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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