International Journal of Odonatology · 2014 · 19 citations · 57 references
Life SciencesBiologyGeneticsConservation GeneticsInvertebrate ZoologyPhylogeographyComparative PhylogeographyPolymerase Chain ReactionCell Division ControlMolecular PhylogeographyNuclear Dna MarkersNuclear Dna PhylogeographyNuclear Genetic MarkersPhylogeographic AnalysisPhylogeographic ConservationPhylogeographic Inference
While phylogeographic data provide valuable information to inform conservation plans, there are comparatively few Odonata phylogeographic studies. This lack of research is partially due to a lack of independent DNA markers with appropriate levels of polymorphism that PCR-amplify in a range of species. We followed an exon-primed, intron-crossing (EPIC) PCR strategy to develop five new, polymorphic nuclear DNA sequence loci (six distinct DNA fragments) for the southern damselfly Coenagrion mercuriale. These markers were: cell division cycle 5 protein (CDC5), arginine methyltransferase (PRMT), acetylglucosaminyl-transferase (AgT), myosin light chain (MLC) and phosphoglucose isomerase (PGI). Between three and five of these new markers could be PCR-amplified in five other species from the genus Coenagrion; one locus (PRMT) can be used in 26 other species of odonates that we examined, including three species of Anisoptera belonging to the genus Onychogomphus. These new nuclear genetic markers will be useful for phylogeographic studies in a range of odonate species, but also for phylogenetic studies, providing a particularly useful complement to the existing mitochondrial and nuclear loci.
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Basic local alignment search tool
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Statistical method for testing the neutral mutation hypothesis by DNA polymorphism.
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