Rearrangement of the nad1 gene in Pristaulacus compressus (Spinola) (Hymenoptera: Evanioidea: Aulacidae) mitochondrial genome.

Mitochondrial Dna Pub Date : 2015-08-01 Epub Date: 2013-10-01 DOI:10.3109/19401736.2013.834436
Shu-Jun Wei, Qiu-Ling Wu, Kees van Achterberg, Xue-Xin Chen
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引用次数: 14

Abstract

The mitochondrial genome of the Pristaulacus compressus (Spinola, 1808) (Hymenoptera: Aulacidae) (GenBank accession No. KF500406) is reported in this study. This is the first sequenced mitochondrial genome from the family Aulacidae of the order Hymenoptera. The length of this mitochondrial genome is 15,563 bp with an A + T content of 84%, including 13 protein-coding, 2 rRNA and 22 tRNA gene, and an A + T-rich region (Table 1). Three tRNA and one protein-coding genes were rearranged in the P. compressus mitochondrial genome, in which, the trnY was inverted, while the trnQ was shuffled to the downstream of tRNA cluster trnI-trnQ-trnM. The trnS1 was translocated to the downstream of the A + T-rich region together with the protein-coding gene nad1. The gene arrangement pattern of this mitochondrial genome is new to the Hymenoptera. All protein-coding genes start with ATN start codon. Ten protein-coding genes stop with termination codon TAA, whereas one protein-coding gene uses incomplete stop codon TA and two use T. The A + T-region is located between rrnS and trnS1 with a length of 780 bp.

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压缩小蜜蜂线粒体基因组nad1基因的重排(膜翅目:叶蜂总科:叶蜂科)。
小蜂(Pristaulacus compressus, Spinola, 1808)线粒体基因组(膜翅目:小蜂科)(GenBank登记号:KF500406)在本研究中被报道。这是第一个从膜翅目蜂科中测序的线粒体基因组。该线粒体基因组全长15563 bp, A + T含量为84%,包括13个蛋白编码基因、2个rRNA基因和22个tRNA基因,以及一个A + T富集区(表1)。压缩白颡鱼线粒体基因组中有3个tRNA和1个蛋白编码基因重排,其中trnY被倒置,trnQ被打乱到tRNA簇trnI-trnQ-trnM的下游。trnS1与蛋白编码基因nad1一起被转移到富A + t区下游。该线粒体基因组的基因排列模式在膜翅目昆虫中是新的。所有蛋白质编码基因都以ATN起始密码子开始。10个蛋白编码基因以终止密码子TAA终止,1个蛋白编码基因使用不完全终止密码子TA, 2个蛋白编码基因使用t。A + t区位于rrnS和trnS1之间,长度为780 bp。
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Mitochondrial Dna
Mitochondrial Dna 生物-遗传学
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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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