Evidence map›Paper›PMID 41087882›Full record

ArticleBMC plant biology2025

SSR genotyping of 200 tea (Camellia sinensis) clones obtained by selection and DNA barcoding of 12 varietal registration candidates.

Ayşenur Eminoğlu, Şule Güzel İzmirli, Fatih Şaban Beriş, Deryanur Dinçer, Keziban Yazıcı

Abstract read
In one paragraph

Article in BMC plant biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

Ayşenur EminoğluDepartment of Biology, Faculty of Art and Science, Division of Molecular Biology, Recep Tayyip Erdoğan University, Rize, Türkiye. aysenur.eminoglu@erdogan.edu.tr.ORCID http://orcid.org/0000-0003-1693-6332
Şule Güzel İzmirliDepartment of Biology, Faculty of Art and Science, Division of Plant Ecology, Recep Tayyip Erdoğan University, Rize, Türkiye.ORCID http://orcid.org/0000-0003-3822-8062
Fatih Şaban BerişDepartment of Biology, Faculty of Art and Science, Division of Molecular Biology, Recep Tayyip Erdoğan University, Rize, Türkiye.ORCID http://orcid.org/0000-0002-0535-943X
Deryanur DinçerDepartment of Landscape Architecture, Faculty of Engineering and Architecture, Division of Plant Material and Cultivation, Recep Tayyip Erdoğan University, Rize, Türkiye.ORCID http://orcid.org/0000-0002-1737-3124
Keziban YazıcıDepartment of Horticulture, Faculty of Agriculture, Division of Horticulture, Recep Tayyip Erdoğan University, Rize, Türkiye.ORCID http://orcid.org/0000-0002-5957-053X

Funding

Türkiye Bilimsel ve Teknolojik Araştırma Kurumu 118G038
6 · The paper itself

Abstract

Genotype and cultivar identification is essential for conserving tea genetic diversity within plantation ecosystems and ensuring the sustainability of high-quality tea production. This study represents the first large-scale genetic characterization of 200 elite varietal candidate tea (Camellia sinensis) clones, which were pre-selected from 2,034 genotypes originating from the Eastern and Western Black Sea regions of Türkiye. Eight polymorphic simple sequence repeat (SSR) markers located near loci associated with catechin content, including epicatechin (EC), epicatechin gallate (ECG), epigallocatechin (EGC), and epigallocatechin gallate (EGCG), were employed. SSR profiles were generated for all 200 tea clones cultivated in control plots at the National Tea Gene Bank, and the resulting data were additionally used for DNA barcoding of 12 varietal candidate tea clones currently under registration. Among the evaluated markers, TM412 (EGC) exhibited the highest polymorphism information content (PIC = 0.8816), whereas TM376 (EC) showed the lowest (0.4321). Notably, TM412 (EGC) and TM399 (ECG) displayed high PIC values, indicating their strong discriminatory potential for Turkish tea genotypes. The findings indicate that Turkish tea germplasm possesses substantial genetic diversity, and some markers may be effectively utilized in variety registration and breeding efforts. This study presents the first comprehensive molecular characterization of tea genetic resources in Türkiye. It contributes to the long-term conservation of selected clones and supports the variety registration process through DNA barcoding and a QR code-based traceability system. The genetic dataset generated in this work contributed directly to the establishment of Türkiye's first and the world's fifth-largest tea gene pool in Rize Province, providing a valuable reference for strengthening tea genetic resource conservation and breeding programs at both national and global scales.

Indexed as

Camellia sinensisDNA Barcoding, TaxonomicMicrosatellite RepeatsGenetic VariationGenotypeGenotyping TechniquesPolymorphism, GeneticCamellia sinensisDNA barcodingGenetic diversitySSR markers (microsatellites)Varietal registration

Identifiers

PMID41087882
PMCPMC12522243

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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.