The complete mitochondrial genome of camphor lace bug, Stephanitis macaona (Hemiptera: Tingidae) and its phylogenetic analysis.

IF 0.7 4区 生物学 Q4 GENETICS & HEREDITY Mitochondrial DNA. Part B, Resources Pub Date : 2025-02-09 eCollection Date: 2025-01-01 DOI:10.1080/23802359.2025.2463500
Tian-Qi Tian, Feng Zhang, Ying-Yan Zhai, Ying-Mei Li, Zeng-Yi Li, Bo Hong
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Abstract

Stephanitis macaona Drake, 1948 (Hemiptera: Tingidae) is an important pest of camphor trees. The complete mitochondrial genome of S. macaona was sequenced and assembled in this paper. The circular genome is 15,407 bp in length and contains 37 genes (13 protein-coding genes, 22 transfer RNA genes, 2 ribosomal RNA genes) as well as one AT-rich region (GenBank accession no. PP868166). The average nucleotide composition is 44.04% for A, 34.40% for T, 12.50% for C, and 9.06% for G. The percentage of A + T contents is 78.44%. The maximum-likelihood phylogenetic analysis of the concatenated nucleotide sequences of 13 PCGs from 21 species in the family Tingidae and two outgroup species was performed. The results indicated that Stephanitis macaona does not form sister relationships with any other species, instead nesting within the genus Stephantis. This study provides significant molecular data for advancing the evolutionary and phylogeographic analysis of S. macaona.

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樟树花虱(半翅目:樟树科)线粒体全基因组及其系统发育分析。
金凤花(半翅目:金凤花科)是樟树的重要害虫。本文对猕猴线粒体全基因组进行了测序和组装。该环状基因组全长15407 bp,包含37个基因(13个蛋白质编码基因,22个转移RNA基因,2个核糖体RNA基因)和1个AT-rich区域(GenBank登录号:PP868166)。A的平均核苷酸组成为44.04%,T为34.40%,C为12.50%,g为9.06%,其中A + T的含量为78.44%。对21种麻蝇科和2个外群种的13个PCGs序列进行了最大似然系统发育分析。结果表明,金凤花不与其他物种形成姐妹关系,而是在金凤花属内筑巢。该研究为推进猕猴的进化和系统地理分析提供了重要的分子数据。
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Mitochondrial DNA. Part B, Resources
Mitochondrial DNA. Part B, Resources Biochemistry, Genetics and Molecular Biology-Molecular Biology
CiteScore
1.30
自引率
20.00%
发文量
670
期刊介绍: This open access journal publishes high-quality and concise research articles reporting the sequence of full mitochondrial genomes, and short communications focusing on the physical, chemical, and biochemical aspects of mtDNA and proteins involved in mtDNA metabolism and interactions.
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