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Construction of fingerprinting for tea plant (Camellia sinensis) accessions using new genomic SSR markers

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Abstract

As one of the most popular non-alcoholic beverage crops, the tea plant (Camellia sinensis) plays an important role in human health and lifestyle. Genetic fingerprinting based on genomic-derived markers in tea, however, is still in the initial stages, which has limited tea germplasm resource utilization and cultivar protection. In the current study, we identified whole genome-based simple sequence repeat (SSR) loci and successfully developed 36 new genomic SSR markers, which are highly polymorphic with average allele number and polymorphic information content (PIC) of 14.9 and 0.862, respectively. A phylogenetic tree for 80 tea plant accessions was subsequently constructed based on their genotypic scores for these 36 markers. The phylogenetic relationships among the 80 accessions are highly consistent with their genetic backgrounds or original places. Noteworthy, robust fingerprinting power was performed, and the overall probability of finding two random individuals sharing identical genotypes across the 36 loci was estimated to be 1.5 × 10−56. We subsequently identified five SSR markers as a recommended core marker set for fingerprinting the tea plant cultivars or accessions. The combined PI and PIsibs of the marker set were 1.49 × 10−9 and 2.57 × 10−3, respectively, which allowed us to fully discriminate all 80 tea plant accessions from one another. The SSR markers developed here will provide a valuable resource for tea plant genetics and genomic studies, as well as breeding programs. The fingerprinting profiles can serve as a database that is essential for the tea industry and commercial breeding, and for tea plant cultivar identification, utilization, and protection.

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References

  • Bali S, Mamgain A, Raina SN, Yadava SK, Bhat V, Das S, Pradhan AK, Goel S (2015) Construction of a genetic linkage map and mapping of drought tolerance trait in Indian beveragial tea. Mol Breed 35:112

    Article  Google Scholar 

  • Bali S, Raina SN, Bhat V, Aggarwal RK, Goel S (2013) Development of a set of genomic microsatellite markers in tea (Camellia L.) (Camelliaceae). Mol Breed 32:735–741

    Article  CAS  Google Scholar 

  • Celik I, Bodur S, Frary A, Doganlar S (2016) Genome-wide SNP discovery and genetic linkage map construction in sunflower (Helianthus annuus L.) using a genotyping by sequencing (GBS) approach. Mol Breed 36:133

  • Chen L, Yu FL, Tong Q, Q. (2000) Discussions on phylogenetic classification and evolution of section Thea. J Tea Sci 20:89–94

    Google Scholar 

  • Fang W, Li X, Cheng H, Duan Y, Jiang X (2012) Genetic diversity and relationship of clonal tea (Camellia sinensis) cultivars in China as revealed by SSR markers. Plant Syst Evol 298:469–483

    Article  Google Scholar 

  • Freeman S, West J, James C, Lea V, Mayes S (2004) Isolation and characterization of highly polymorphic microsatellites in tea (Camellia sinensis). Mol Ecol Notes 4:324–326

    Article  CAS  Google Scholar 

  • Hashimoto M, Takasi S (1978) Morphological studies on the origin of the tea plant V, a proposal of one place of origin by cluster analysis. Jpn J Crop Agr 21:93–101

    Google Scholar 

  • Huang H, Tong Y, Zhang QJ, Gao LZ (2013) Genome size variation among and within Camellia species by using flow cytometric analysis. PLoS One 8:e64981

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Kaundun SS, Matsumoto S (2004) PCR-based amplicon length polymorphisms (ALPs) at microsatellite loci and indels from non-coding DNA regions of cloned genes as a means of authenticating commercial Japanese green teas. J Sci Food Agric 84:895–902

    Article  CAS  Google Scholar 

  • Liu K, Musel SV (2005) PowerMarker: an integrated analysis environment for genetic marker analysis. Bioinformatics 21:2128–2129

    Article  CAS  PubMed  Google Scholar 

  • Liu SR, Li WY, Long D, Hu CG, Zhang JZ (2013) Development and characterization of genomic and expressed SSRs in citrus by genome-wide analysis. PLoS One 8:e75149

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Ma JQ, Yao MZ, Ma CL, Wang XC, Jin JQ, Wang XM, Chen L (2014) Construction of a SSR-based genetic map and identification of QTLs for catechins content in tea plant (Camellia sinensis). PLoS One 9:e93131

    Article  PubMed  PubMed Central  Google Scholar 

  • Ma JQ, Zhou YH, Ma CL, Yao MZ, Jin JQ, Wang XC, Chen L (2010) Identification and characterization of 74 novel polymorphic EST-SSR markers in the tea plant, Camellia sinensis (Theaceae). Am J Bot 97:e153–e156

    Article  CAS  PubMed  Google Scholar 

  • Mukhopadhyay M, Mondal TK, Chand PK (2016) Biotechnological advances in tea (Camellia sinensis [L.] O. Kuntze): a review. Plant Cell Rep 35:255–287

    Article  CAS  PubMed  Google Scholar 

  • Nei M, Tajima F, Tateno Y (1983) Accuracy of estimated phylogenetic trees from molecular data. J Mol Evol 19:153–170

    Article  CAS  PubMed  Google Scholar 

  • Ni S, Yao MZ, Chen L, Zhao LP, Wang XC (2008) Germplasm and breeding research of tea plant based on DNA marker approaches. Front Agric China 2:200–207

    Article  Google Scholar 

  • Nimmakayala P, Abburi VL, Abburi L, Alaparthi SB, Cantrell R, Park M, Choi D, Hankins G, Malkaram S, Reddy UK (2014) Linkage disequilibrium and population-structure analysis among Capsicum annuum L. cultivars for use in association mapping. Mol Gen Genomics 289:513–521

    Article  CAS  Google Scholar 

  • Patzak J, Vrba L, Matousek J (2007) New STS molecular markers for assessment of genetic diversity and DNA fingerprinting in hop (Humulus lupulus L.) Genome 50:15–25

    Article  CAS  PubMed  Google Scholar 

  • Peakall R, Smouse PE (2012) GenAlEx 6.5: genetic analysis in Excel. Population genetic software for teaching and research—an update. Bioinformatics 28:2537–2539

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Sardar SS, Pradhan K, Shukla RP, Saraswat R, Srivastava A, Jena SN, Das AB (2016) In silico mining of EST-SSRs in Arachis hypogaea L. and their utilization for genetic structure and diversity analysis in cultivars/breeding lines in Odisha, India. Mol Breed 36:49

  • Sharangi AB (2009) Medicinal and therapeutic potentialities of tea (Camellia sinensis L.)—a review. Food Res Int 42:529–535

    Article  CAS  Google Scholar 

  • Singh NV, Abburi VL, Ramajayam D, Kumar R, Chandra R, Sharma KK, Sharma J, Babu KD, Pal RK, Mundewadikar DM, Saminathan T, Cantrell R, Nimmakayala P, Reddy UK (2015) Genetic diversity and association mapping of bacterial blight and other horticulturally important traits with microsatellite markers in pomegranate from India. Mol Gen Genomics 290:1393–1402

    Article  CAS  Google Scholar 

  • Tamura K, Dudley J, Nei M, Kumar S (2007) MEGA4: molecular evolutionary genetics analysis (MEGA) software version 4.0. Mol Biol Evol 24:1596–1599

    Article  CAS  PubMed  Google Scholar 

  • Tan LQ, Peng M, Xu LY, Wang LY, Chen SX, Zou Y, Qi GN, Cheng H (2015) Fingerprinting 128 Chinese clonal tea cultivars using SSR markers provides new insights into their pedigree relationships. Tree Genet Genomes 11:90

    Article  Google Scholar 

  • Tan LQ, Wang LY, Xu LY, Wu LY, Peng M, Zhang CC, Wei K, Bai PX, Li HL, Cheng H, Qi GN (2016) SSR-based genetic mapping and QTL analysis for timing of spring bud flush, young shoot color, and mature leaf size in tea plant (Camellia sinensis). Tree Genet Genomes 12:52

    Article  Google Scholar 

  • Tanaka J, Taniguchi F (2006) Estimation of the genome size of tea (Camellia sinensis), Camellia (C. japonica), and their interspecific hybrids by flow cytometry. J Remote Sens Soc Jpn 101:1–7

    Google Scholar 

  • Taniguchi F, Furukawa K, Metoku SO, Yamaguchi N, Ujihara T, Kono I, Fukuoka H, Tanaka J (2012) Construction of a high-density reference linkage map of tea (Camellia sinensis). Breed Sci 62:263–273

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Tautz D, Renz M (1984) Simple sequences are ubiquitous repetitive components of eukaryotic genomes. Nucleic Acids Res 12:4127–4138

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Ujihara T, Ohta R, Hayashi N, Kohata K, Tanaka J (2009) Identification of Japanese and Chinese green tea cultivars by using simple sequence repeat markers to encourage proper labeling. Biosci Biotechnol Biochem 73:15–20

    Article  CAS  PubMed  Google Scholar 

  • Ujihara T, Taniguchi F, Tanaka J, Hayashi N (2011) Development of expressed sequence tag (EST)-based cleaved amplified polymorphic sequence (CAPS) markers of tea plant and their application to cultivar identification. J Agric Food Chem 59:1557–1564

    Article  CAS  PubMed  Google Scholar 

  • Waits LP, Luikart G, Taberlet P (2001) Estimating the probability of identity among genotypes in natural populations: cautions and guidelines. Mol Ecol 10:249–256

    Article  CAS  PubMed  Google Scholar 

  • Wambulwa MC, Meegahakumbura MK, Chalo R, Kamunya S, Muchugi A, Xu JC, Liu J, Li DZ, Gao LM (2016) Nuclear microsatellites reveal the genetic architecture and breeding history of tea germplasm of East Africa. Tree Genet Genomes 12:11

    Article  Google Scholar 

  • Yang CS, Wang X, Lu G, Picinich SC (2009) Cancer prevention by tea: animal studies, molecular mechanisms and human relevance. Nat Rev Cancer 9:429–439

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Yang H, Wei CL, Liu HW, Wu JL, Li ZG, Zhang L, Jian JB, Li YY, Tai YL, Zhang J, Zhang ZZ, Jiang CJ, Xia T, Wan XC (2016) Genetic divergence between Camellia sinensis and its wild relatives revealed via genome-wide SNPs from RAD sequencing. PLoS One 11:e0151424

    Article  PubMed  PubMed Central  Google Scholar 

  • Yang YJ, Liang YR (2014) Clonal tea cultivars in China. Shanghai Scientific and Technical Publishers, Shanghai

    Google Scholar 

  • Yao MZ, Ma CL, Qiao TT, Jin JQ, Chen L (2012) Diversity distribution and population structure of tea germplasms in China revealed by EST-SSR markers. Tree Genet Genomes 8:205–220

    Article  Google Scholar 

  • Zhang JZ, Liu SR, Hu CG (2016) Identifying the genome-wide genetic variation between precocious trifoliate orange and its wild type and developing new markers for genetics research. DNA Res 23:403–414

    Article  CAS  PubMed  PubMed Central  Google Scholar 

Download references

Acknowledgments

This work was supported by the National Natural Science Foundation of China (31171608), the Special Innovative Province Construction in Anhui Province (15czs08032), the Central Guiding the Science and Technology Development of the Local (2016080503B024), and the Anhui Natural Science Foundation (1608085J08, 1608085QC57). We appreciate the anonymous reviewers for constructive comments on this manuscript.

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Authors and Affiliations

Authors

Contributions

SRL performed collections of tea plant materials, data analysis, and manuscript drafting. HWL involved in DNA isolation, designing genomic SSRs primers, SSR genotyping, PCR amplifications, and testing amplified fragments. ALW and YH coordinated collections of plant materials and DNA isolation. YLA involved in PCR amplifications and testing amplified fragments. CLW involved in experimental design, data analysis, and manuscript preparation.

Corresponding author

Correspondence to Chaoling Wei.

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The authors declare that they have no competing interests.

Electronic supplementary material

Online Resource 1

Geographic distribution of the 80 tea accessions used in this study. Numbers in parentheses indicate the number of accessions collected from each 13 provinces of China (JPEG 708 kb)

Online Resource 2

Screening of the 36 primer pairs against six selected tea cultivars on 1.5% agarose gels. The cultivars numbered 1 to 6 are ‘Tieguanyin’, ‘Shuchazao’, ‘Longjingchangye’, ‘Yungui’, ‘Yunkang 10’ and ‘Yunmei’, respectively (JPEG 1036 kb)

Online Resource 3

Details of 36 oligonucleotide SSR primer pairs including marker name, type and number of repeat motifs, forward and reverse primer sequences, and expected amplicon sizes (DOCX 17 kb)

Online Resource 4

The fingerprinting profiles of the 80 tea accessions based on five SSR markers (DOCX 21 kb)

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Liu, S., Liu, H., Wu, A. et al. Construction of fingerprinting for tea plant (Camellia sinensis) accessions using new genomic SSR markers. Mol Breeding 37, 93 (2017). https://doi.org/10.1007/s11032-017-0692-y

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