Abstract

We generated a phylogeny for Caucasian rock lizards (Darevskia), and included six other families of true lizards (Lacertini), based on complete mitochondrial genome analysis. Next-generation sequencing (NGS) of genomic DNA was used to obtain 16 new mitogenomes of Darevskia. These, along with 35 sequences downloaded from GenBank: genera Darevskia, Zootoca, Podarcis, Phoenicolacerta, Takydromus, Lacerta, and Eremias-were used in the analysis. All four analytical methods (Bayesian Inference, BI; Maximum Likelihood, ML; Maximum Parsimony, MP; and Neighbor-Joining, NJ) showed almost congruent intra-generic topologies for Darevskia and other lizard genera. However, ML and NJ methods on one side, and BI and MP methods on the other harvested conflicting phylogenies. The ML/NJ topology supports earlier published separation of Darevskia into three mitochondrial clades (Murphy, Fu, Macculloch, Darevsky, and Kupinova, 2000), but BI and MP topologies support that the basal branching occurred between D. parvula from the western Lesser Caucasus and the rest of Darevskia. All topologies altered the phylogenetic position of some individual species, including D. daghestanica, D. derjugini, and D. chlorogaster. Reanalysis after excluding four saturated genes from the data set, and excluding genus Eremias gives fully convergent topologies. The most basal branching for true lizards was between Far Eastern Takydromus and the Western Eurasian genera (BI). Comparing phylogenetic performance of individual genes relative to whole mitogenome data, concatenated 16S RNA (the least saturated gene in our analyses) and Cytochrome b genes generate a robust phylogeny that is fully congruent with that based on the complete mitogenome.

Highlights

  • MethodsTissue samples (tail tips) were obtained from live individuals collected from 15 locations in Georgia and one in Azerbaijan

  • Sequences of complete mitochondrial DNAs of Darevskia species were deposited in GenBank with accession numbers MH481130-37; MG704915-21

  • NADH 5 starts with ACC in species: D. mixta, D.dahli, D. armeniaca, D. caucasica and D. clarkorum, with ATC in D. chlorogaster and D. derjugini, GTG in D. parvula and ACA in D. praticola

Read more

Summary

Methods

Tissue samples (tail tips) were obtained from live individuals collected from 15 locations in Georgia and one in Azerbaijan. The individuals represent 14 bisexual species and two parthenogenetic forms of Darevskia (Fig 1). The tail-tips were preserved in 95% ethanol. DNA was extracted from the samples using Qiagen DNeasy Blood and Tissue Kit, according to the manufacturer’s instructions (DNeasy Blood & Tissue Handbook 07/2006, [36]). To check for contamination, a negative control (reagents only) was included during extractions, and tested for amplification during PCR

Results
Discussion
Conclusion
Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.