Evidence map›Paper›PMID 42469642›Full record

ArticleBMC plant biology2026

Comparative chloroplast genome analysis reveals genetic differentiation and maternal introgression in tea plants (Camellia sinensis) from Shaoyang, China.

Jin Li, Ni Zhong, Yu Qin, Chang-Qing Xie, Han Tang, Ai-Ming Tang, Hua Luo

Abstract readComparative Study
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Article in BMC plant biology, 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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7 authors.

Jin LiInstitute of Tea Research, Shaoyang Academy of Agricultural Sciences, Shaoyang, China.
Ni ZhongInstitute of Tea Research, Hunan Academy of Agricultural Sciences, Changsha, China.
Yu QinCollege of Applied Technology, Hunan Open University, Changsha, China.
Chang-Qing XieInstitute of Tea Research, Shaoyang Academy of Agricultural Sciences, Shaoyang, China.
Han TangInstitute of Tea Research, Shaoyang Academy of Agricultural Sciences, Shaoyang, China.
Ai-Ming TangXinning County Shun Di Tea Industry Co., LTD, Shaoyang, China.
Hua LuoInstitute of Tea Research, Shaoyang Academy of Agricultural Sciences, Shaoyang, China. shaoyangnky@163.com.

Funding

Natural Science Foundation of Hunan Province S2024JJQYLH0589Natural Science Research Fund of Shaoyang City 2024PT4071
6 · The paper itself

Abstract

backgroundAlthough the tea germplasm resources in the Shaoyang area of south-west Hunan Province, China, are extremely diverse, knowledge of the maternal lineages and adaptive evolution of these resources is still limited. The genetic relationship of the populations in Tingping Township (Chengbu County) has long been a focus of attention, but due to insufficient genetic information, it was not determined to which branch they belonged in the phylogenetic tree.

resultsBy integrating the newly sequenced chloroplast genomes of Tingping tea plants with nine other accessions, we built a robust dataset comprising 15 samples that representing the broader area of Shaoyang. These plastomes range in size from 156,697 to 157,098 bp and have the typical quadripartite structure. Comparative genomic analysis of these chloroplast genomes revealed high sequence conservation (90-100% identity) with no rearrangements or large indels, yet identified 19 hypervariable intergenic regions (e.g., trnH-psbA, trnC-petN, ndhF-rpl32) and five divergent protein-coding genes (rpoC2, ycf2, ndhB, ccsA, ndhE) concentrated in non-coding regions. Analysis of inverted repeat (IR) dynamics uncovered three distinct structural architectures-standard type, IR-contracted type, and wild-specialized type-suggesting a more complex evolutionary trajectory than initially assumed. Based on statistical analyses using the PAML branch-site model, chloroplast genes in the target clade were not subject to positive selection, further supporting the view that the chloroplast genome is highly conserved. Our phylogeny also reveals a significant "West Large vs East Small" leaf type division. The Tingping samples exhibit a mosaic maternal ancestry comprising both var. assamica and var. sinensis chloroplast lineages, indicating that this region has experienced complex historical gene flow, likely associated with cultivation and seed exchange. These chloroplast genome patterns are consistent with maternal lineage introgression (chloroplast capture), although nuclear markers would be required to confirm true introgression and to distinguish ancient divergence from recent admixture.

conclusionsThis study provides the map of the maternal genetic structure of Shaoyang tea plants. The discovery of a distinct maternal lineage in 'zhuyedong' and complex patterns consistent with chloroplast capture in Tingping not only restructures our understanding of local tea evolution but also provides an indispensable genetic basis for the conservation of gene pools and the breeding of excellent tea varieties.

Indexed as

Camellia sinensisGenetic IntrogressionGenetic VariationGenome, ChloroplastChinaEvolution, MolecularPhylogenyCamellia sinensisChloroplast captureChloroplast genomeGenetic differentiationPhylogeny

Identifiers

PMID42469642
PMCPMC13660146

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