Evidence map›Paper›PMID 41790309›Full record

ArticleMolecular biology reports2026

Identification of plastome-derived mini barcodes by DNA metabarcoding and comparative effectiveness to decipher their strength and resolving power for taxonomic topology-based phylogenetic determination of Chenopodium quinoa.

Zakia Habib, Siddra Ijaz, Imran Ul Haq, Irfan Afzal, Ghulam Muhammad Ali

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Article in Molecular biology reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 authors.

Zakia HabibCentre of Agricultural Biochemistry and Biotechnology (CABB), University of Agriculture, University Road, Faisalabad, Pakistan.
Siddra IjazCentre of Agricultural Biochemistry and Biotechnology (CABB), University of Agriculture, University Road, Faisalabad, Pakistan. siddraijazkhan@yahoo.com.
Imran Ul HaqDepartment of Plant Pathology, University of Agriculture, University Road, Faisalabad, Pakistan.
Irfan AfzalDepartment of Agronomy, University of Agriculture, University Road, Faisalabad, Pakistan.
Ghulam Muhammad AliPakistan Agricultural Research Council (PARC), Islamabad, Pakistan.

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6 · The paper itself

Abstract

backgroundDiversification of cropping systems with orphan crops directly concerns food security issues. Chenopodium species display a high degree of morphological semblance, which makes their taxonomic identification intricate and challenging. METHODS AND

resultsDNA barcoding of Chenopodium quinoa was made to characterize crop material imported through international trade for the prevailing cropping system. The phylogenetic reconstruction analysis using standard DNA barcodes rbcL and matK did not yield an optimal divergence threshold to resolve C. quinoa from other closely related Chenopodium species. Hence, identifying candidate DNA barcodes for resolving taxonomic diversity is a pressing need. Therefore, this study explored several candidate regions with low intraspecific but high interspecific divergence, and fourteen hypervariable regions were identified as candidate DNA barcodes. These hypervariable regions exhibit significant nucleotide diversity. The phylogenetic analysis revealed that candidate DNA barcodes possess an optimal divergence threshold compared to standard DNA barcodes and have shown more potential to delineate C. quinoa accessions as residents of an evolutionary distinct clade from other Chenopodium species. Mini-barcodes were developed from two hypervariable regions: the trnT(UGU)-trnL(UAA) intergenic spacer region and the rpl32-trnL region. These proved to have significant qualitative and quantitative identity accuracy for two C. quinoa and C. album seed experimental mixtures.

conclusionThe standard DNA barcodes were insufficient to discriminate C. quinoa from other Chenopodium species whereas the candidate DNA barcodes and developed mini-barcodes showed high accuracy in species discrimination and germplasm authentication.

Indexed as

Chenopodium quinoaDNA Barcoding, TaxonomicPlastidsDNA, PlantGenetic VariationPhylogenySequence Analysis, DNADNA, PlantChloroplast genomeDivergence hotspot regionsNucleotide diversityPhylogenetic analysis

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