DNA Barcoding Analysis and Phylogenetic Position of Endemic Lysimachia savranii Species

In this study, DNA barcode analysis and phylogenetic position of endemic species Lysimachia savranii were determined using nrDNA ITS and cpDNA rbcL sequences. Green leaves of endemic L. savranii were brought to the laboratory and genomic DNA was isolated. ITS (ITS5A and ITS4) and rbcL (rbcLaF and rbcLaR) primers were used to perform the PCR amplifications. Using BioEdit 7.2.3 and FinchTV 1.4.0, forward and reverse sequences were checked and corrected and then blasted at NCBI. For phylogenetic analyses, different species were taken from NCBI and phylogenetic trees as well as genetic distance values were revealed. The ITS sequence length was determined to be 661 nt while the rbcL sequence length was 548 nt. In both the ITS and rbcL results, L. savranii was found to be genetically closest to the L. serpyllifolia species. In the phylogenetic analysis results, L. savranii appeared in a group with L. serpyllifolia, L. nemorum and Anagilis arvensis species. Additionally, previously studies conducted revealed that Lysimachia is a paraphyletic group and this is supported by our results.

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Journal
Bulletin of University of Agricultural Sciences and Veterinary Medicine Cluj-Napoca Agriculture
Published
2025-05-15
DOI
https://doi.org/10.15835/buasvmcn-agr:2024.0003
Primary Topic
Identification and Quantification in Food
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article
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article

DNA Barcoding Analysis and Phylogenetic Position of Endemic Lysimachia savranii Species

İsa BAŞKÖSE, Emre Sevindik
Bulletin of University of Agricultural Sciences and Veterinary Medicine Cluj-Napoca Agriculture
Identification and Quantification in Food
article

DNA Barcoding Analysis and Phylogenetic Position of Endemic Lysimachia savranii Species

İsa BAŞKÖSE, Emre Sevindik
article en

Abstract

In this study, DNA barcode analysis and phylogenetic position of endemic species Lysimachia savranii were determined using nrDNA ITS and cpDNA rbcL sequences. Green leaves of endemic L. savranii were brought to the laboratory and genomic DNA was isolated. ITS (ITS5A and ITS4) and rbcL (rbcLaF and rbcLaR) primers were used to perform the PCR amplifications. Using BioEdit 7.2.3 and FinchTV 1.4.0, forward and reverse sequences were checked and corrected and then blasted at NCBI. For phylogenetic analyses, different species were taken from NCBI and phylogenetic trees as well as genetic distance values were revealed. The ITS sequence length was determined to be 661 nt while the rbcL sequence length was 548 nt. In both the ITS and rbcL results, L. savranii was found to be genetically closest to the L. serpyllifolia species. In the phylogenetic analysis results, L. savranii appeared in a group with L. serpyllifolia, L. nemorum and Anagilis arvensis species. Additionally, previously studies conducted revealed that Lysimachia is a paraphyletic group and this is supported by our results.

Bulletin of University of Agricultural Sciences and Veterinary Medicine Cluj-Napoca AgricultureVol. 82(1)
Ankara University (TR), Adnan Menderes University (TR)
Openalex Percentile: Top 89%
Identification and Quantification in Food
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