The extraordinary rearrangement of mitochondrial genome of the wheat pest, Aptinothrips stylifer and the mitochondrial phylogeny of Thripidae (Thysanoptera)

Author:

Li Chengwen1ORCID,Gao Yuxin1ORCID,Wang Dongxue1ORCID,Dang Lihong1234ORCID

Affiliation:

1. Department of Biology, School of Bioscience and Engineering Shaanxi University of Technology Hanzhong China

2. Shaanxi Province Key Laboratory of Bio‐Resources Hanzhong China

3. Qinba Mountain Area Collaborative Innovation Center of Bioresources Comprehensive Development Hanzhong China

4. Qinba State Key Laboratory of Biological Resources and Ecological Environment (Incubation) Hanzhong China

Abstract

AbstractThe mitochondrial gene order in Thysanoptera is notably distinct and highly rearranged, with each species exhibiting its own unique arrangement. To elucidate the relationship between gene rearrangements and phylogeny, the complete mitochondrial genome (mitogenome) of the wheat pest, Aptinothrips stylifer, was sequenced and assembled, spanning a total length of 16,033 bp. Compared with the ancestral arthropod mitogenome, significant rearrangement differences were evident in A. stylifer, whereas the gene order between A. stylifer and Anaphothrips obscurus was similar. Phylogenetic trees were reconstructed based on all 13 protein‐coding gene sequences using Bayesian inference and maximum‐likelihood methods, both yielding similar topological structures. Notably, A. stylifer was robustly clustered with A. obscurus, affirming its classification within Anaphothrips genus group. This exemplifies the potential correlation between gene rearrangements and phylogeny in the Thripidae family. Additionally, the mitogenome of A. stylifer exhibited several atypical features, including: (1) Three putative control regions (CRs) in close proximity, with CR2 and CR3 displaying partial similarity, and CR1 differing in base composition; (2) Two transfer RNAs (tRNAs), trnS1 and trnV, lacking the DHU arm; (3) Two ribosomal RNA (rRNA) genes inverted and positioned distant from each other; (4) Negative AT and GC skew (AT skew = −0.001, GC skew = −0.077); (5) One transposition (nad6), one inverse transposition (trnQ), four inversions (trnF, trnH, trnC, and gene block nad1‐trnL1‐rrnL‐trnV‐rrnS), and four tandem duplication random loss events; and (6) Two protein‐coding genes, nad2 and atp8, terminated with an incomplete stop codon “T”.

Publisher

Wiley

Subject

Insect Science,General Medicine,Biochemistry,Physiology

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