4.5 Article

Nuclear copies of mitochondrial DNA as a potential problem for phylogenetic and population genetic studies of Odonata

期刊

SYSTEMATIC ENTOMOLOGY
卷 47, 期 4, 页码 591-602

出版社

WILEY
DOI: 10.1111/syen.12550

关键词

cytochrome c oxidase subunit 1; mitogenome; mitophylogenomics; NUMTs; Leucorrhinia albifrons; Odonata

资金

  1. Grant Agency of the University of Ostrava [SGS14/PrF/2021]
  2. Charles University Research Centre program [204069]

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This study discusses the risks and limitations of using mitochondrial markers for taxonomic identification and biodiversity monitoring in Odonata, revealing that NUMTs can have a serious impact on molecular studies of Odonata, especially when the barcode is located in the cox1 gene. It is suggested that nad1 should be used alone or in combination with cox1 to minimize unintended confusion with NUMTs.
The use of mitochondrial markers for taxonomic identification and biodiversity monitoring is not without risks or limitations. Most importantly, the natural transfer of DNA from the mitochondria to the nucleus generates nonfunctional nuclear copies of mitochondrial DNA (NUMTs). Their abundance and size vary significantly among taxa, and NUMTs have been reported to complicate molecular studies based on mitochondrial markers in several insect orders, most prominently in Orthoptera. The significance of this phenomenon in Odonata has not yet been properly addressed. Here, we present a complete mitochondrial genome and a draft nuclear genome of Leucorrhinia albifrons (Odonata: Libellulidae), as well as NUMT and cox1 sequences from the related species Leucorrhinia dubia. We document the presence of NUMTs in the L. albifrons nuclear genome and in nuclear genomes of two other Odonata species available in public databases. Our results show that NUMTs can have a serious impact on barcoding, phylogenetic, population and phylogeographic studies of Odonata, especially when the barcode is located in the cox1 gene, the most frequently used molecular marker for Odonata. We suggest that nad1 should be used alone or in combination with cox1 to minimize unintended confusion with NUMTs. Finally, we present a mitophylogenomic analysis of Odonata and document several cases of misidentified mitochondrial genomes belonging to species different from those indicated in public databases. In conclusion, our findings represent an important step for future metabarcoding studies of Odonata based on mitochondrial DNA markers.

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