Evidence map›Paper›PMID 39190119›Full record

ArticleInternational journal of legal medicine2025

Development of a diagnostic variable number tandem repeat marker and dual TaqMan genotyping assay to distinguish Lophophora species.

Eun-Mi Hwang, Kyu-Sik Jeong, Seong Yeon Yoo, Jihyun Kim, Sanggil Choe, Joo-Young Kim

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Article in International journal of legal medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

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2citing papers in PubMed
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1 · What the graph read from it

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3 · Its place in the literature

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2 citing papers in PubMed.

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  2. The complete chloroplast genome sequence ofMitochondrial DNA. Part B, Resources · 2026
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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Eun-Mi HwangForensic DNA Division, National Forensic Service, Wonju, 26460, Republic of Korea.
Kyu-Sik JeongForensic DNA Division, National Forensic Service, Wonju, 26460, Republic of Korea.
Seong Yeon YooForensic DNA Division, National Forensic Service, Wonju, 26460, Republic of Korea.
Jihyun KimForensic Toxicology and Chemistry Division, Seoul Institute, National Forensic Service, Seoul, 08036, Republic of Korea.
Sanggil ChoeForensic Toxicology Division, National Forensic Service, Wonju, 26460, Republic of Korea.
Joo-Young KimForensic DNA Division, National Forensic Service, Wonju, 26460, Republic of Korea. jykim7112@korea.kr.ORCID http://orcid.org/0000-0003-0594-6754

Funding

National Forensic Service NFS2023DNA01National Forensic Service NFS2023STR02
6 · The paper itself

Abstract

The Lophophora genus of the Cactaceae family includes Lophophora diffusa and Lophophora williamsii, which has traditionally been used as a natural analgesic; however, its use is now under strict regulation worldwide as it contains mescaline, a unique psychotropic agent. Recently, non-medical and illegal distribution and abuse of L. williamsii have increased worldwide; thus, effective species identification methods are urgently needed. Here, we identified a new variable number tandem repeat (VNTR) marker in the trnL intron region to identify and characterize species in forensic analyses. The VNTR marker has a unique structure of tandem repeats, each with 13 nucleotides; one repeat unit was found in L. williamsii and two in L. diffusa. Phylogenetic and length polymorphism analyses confirmed that this novel VNTR marker could distinguish between Lophophora species. Furthermore, our newly developed TaqMan genotyping assay utilizes two probes; the color and position of dots on the discrimination plot differ according to the tandem repeat count within the VNTR marker. The limits of detection of the assay were 0.000063 ng (LW-VNTR probe-1) and 0.000066 ng (LW-VNTR probe-2), indicating high sensitivity. Moreover, when crime scene samples of 16 presumed L. williamsii species were analyzed, the results coincided with those of gas chromatography-mass spectrometry, confirming the applicability of our marker for Lophophora species identification. Thus, the tandem repeats within the trnL intron region can be exploited as a VNTR marker to identify L. williamsii and L. diffusa. Our dual TaqMan genotyping assay based on a novel marker demonstrates potential for forensic applications.

Indexed as

Genotyping TechniquesMinisatellite RepeatsDNA, PlantGenetic MarkersGenotypeHumansIntronsPhylogenySpecies SpecificityDNA, PlantGenetic MarkersLocked nucleic acidLophophora diffusaLophophora williamsiiMescalineTaqMan genotyping assayVariable number tandem repeats

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.