Skip to main content
Log in

Genetic diversity and relationships of wild and cultivated Zanthoxylum germplasms based on sequence-related amplified polymorphism (SRAP) markers

  • Research Article
  • Published:
Genetic Resources and Crop Evolution Aims and scope Submit manuscript

Abstract

The genus Zanthoxylum, belonging to Rutaceae, has a long history of cultivation both for economic and chemical values in China. To effectively conserve and sustainably utilize this genus resource, a study on genetic diversity and relationships of Zanthoxylum germplasms was carried out by employing SRAP markers. We used 16 primer combinations to assess genetic variations and relationships among 175 accessions from eight cultivated provenances, including Shandong, Henan, Shanxi, Shaanxi, Gansu, Sichuan, Guizhou and Yunnan. A total of 145 clear repetitive and intense bands were yielded, and the percentage of polymorphic bands was 100 % for per primer combination, indicating a relatively high diversity among Zanthoxylum germplasms. From a geographic perspective, the highest genetic diversity level was observed within Guizhou provenance (N a  = 1.97, Ne = 1.52, H = 0.31, I = 0.46) while Henan provenance had the lowest genetic diversity (N a  = 1.68, Ne = 1.45, H = 0.25, I = 0.37). Based on AMOVA results, the abundant genetic variation was mainly caused by variation of intra-provenances (84.96 %), rather than among provenances (15.038 %). The results indicated low genetic differentiation (G st  = 0.133) and high gene flow (N m  = 3.2605) among provenances. The neighbor-joining tree revealed that the 175 accessions could be divided into four groups, and groupings indicated a divergence between the cultivated accessions of Zanthoxylum bungeanum Maxim. and Z. armatum DC. Moreover, three accessions of Z. piperitum DC. var. inerme without prickles introduced from Japan gathered one cluster. Cluster IV is composed of accessions of different geographical origin, including 11 wild species and 10 cultivated accessions of Z. bungeanum. The cluster analysis also reflected a relatively close relationship between the geographical origins and the classification of accessions in cluster I. Structure analysis indicated that collected Zanthoxylum accessions could be divided into two major groups. The information obtained from our research would benefit to make use of Zanthoxylum germplasms and assist the management of a Zanthoxylum germplasms collection.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Institutional subscriptions

Fig. 1
Fig. 2
Fig. 3
Fig. 4

Similar content being viewed by others

References

  • Aneja B, Yadav NR, Chawla V, Yadav RC (2012) Sequence-related amplified polymorphism (SRAP) molecular marker system and its applications in crop improvement. Mol Breed 30:1635–1648

    Article  CAS  Google Scholar 

  • Babaei S, Talebi M, Bahar M, Zeinali H (2014) Analysis of genetic diversity among saffron (Crocus sativus) accessions from different regions of Iran as revealed by SRAP markers. Sci Hortic 171:27–31

    Article  CAS  Google Scholar 

  • Ceylan A, Öcal N, Akbulut M (2014) Genetic diversity among the Turkish common bean cultivars (Phaseolus vulgaris L.) as assessed by SRAP, POGP and cpSSR markers. Biochem Syst Ecol 54:219–229

    Article  CAS  Google Scholar 

  • Chen JJ, Lin YH, Day SH, Hwang TL, Chen IS (2011) New benzenoids and anti-inflammatory constituents from Zanthoxylum nitidum. Food Chem 125:282–287

  • Deng HP, Xu J, Chen F, Song QZ (2008) Morphological and molecular identification on genetic diversity of Zanthoxylum armatum var. novemfolius. Acta Bot Boreali-Occidential Sinica 10:2103–2109

    Google Scholar 

  • Dong P, Wei YM, Chen GY, Li W, Wang JR, Nevo E, Zheng YL (2010) Sequence-related amplified polymorphism (SRAP) of wild emmer wheat (Triticum dicoccoides) in Israel and its ecological association. Biochem Syst Ecol 38:1–11

    Article  CAS  Google Scholar 

  • Evanno G, Regnaut S, Goudet J (2005) Detecting the number of clusters of individuals using the software STRUCTURE: a simulation study. Mol Ecol 14:2611–2620

    Article  CAS  PubMed  Google Scholar 

  • Excoffier L, Laval G, Schneider S (2005) Arlequin (version 3.0): an integrated software package for population genetics data analysis. Evol Bioinform online 1:47–50

    PubMed Central  CAS  Google Scholar 

  • Guo DL, Zhang JY, Liu CH, Zhang GH, Li M, Zhang Q (2012) Genetic variability and relationships between and within grape cultivated varieties and wild species based on SRAP markers. Tree Genet Genomes 8:789–800

    Article  Google Scholar 

  • Gupta DD, Mandi SS (2013) Species Specific AFLP Markers for authentication of Zanthoxylum acanthopodium & Zanthoxylum oxyphyllum. J Med Plants 1:1–9

    CAS  Google Scholar 

  • Hamrick JL, Godt MJW, Sherman-Broyles SL (1992) Factors influencing levels of genetic diversity in woody plant species. New For 6:95–124

    Article  Google Scholar 

  • Han SZ, Wang YK, Li J, He CY, Zhou QQ, Zhao D (2011) ISSR genetic diversity analysis of Zanthoxylum bungeanum in Gansu Province. J Gansu Agric Univ 46:46–51

    CAS  Google Scholar 

  • Huang C (1997) Reipublicae popularis sinicae. In: Delectis florae reipublicae popularis sinicae agendae academiae sinicae edita. Science Press, Beijing, pp 8–10

  • Ji JJ, Huang W, Yin YX, Li Z, Gong ZH (2014) Development of a SCAR marker for early identification of S-cytoplasm based on mitochondrial SRAP analysis in pepper (Capsicum annuum L.). Mol Breed 33:679–690

    Article  CAS  Google Scholar 

  • Jing ZB, Ruan XF, Wang RZ, Yang Y (2013) Genetic diversity and relationships between and within persimmon (Diospyros L.) wild species and cultivated varieties by SRAP markers. Plant Syst Evol 299:1485–1492

    Article  Google Scholar 

  • Liu Y, Zhang JM, Wang XG, Liu F, Shen ZB (2013) Genetic diversity in Vicia amoena (Fabaceae) germplasm resource in China using SRAP and ISSR markers. Biochem Syst Ecol 51:86–93

    Article  CAS  Google Scholar 

  • Mahar KS, Rana TS, Ranade SA, Meena B (2011) Genetic variability and population structure in Sapindus emarginatus Vahl from India. Gene 485:32–39

    Article  CAS  PubMed  Google Scholar 

  • Milla-Lewis SR, Kimball JA, Zuleta MC, Harris-Shultz KR, Schwartz BM, Hanna WW (2012) Use of sequence-related amplified polymorphism (SRAP) markers for comparing levels of genetic diversity in centipedegrass (Eremochloa ophiuroides (Munro) Hack.) germplasm. Genet Resour Crop Evol 59:1517–1526

    Article  CAS  Google Scholar 

  • Nagai H, Yoshida T, Kamiya K, Yahara T, Tachida H (2009) Development and characterization of microsatellite markers in Zanthoxylum ailanthoides (Rutaceae). Mol Ecol Resour 9:667–669

    Article  CAS  PubMed  Google Scholar 

  • Pollegioni P, Woeste K, Olimpieri I, Marandola D, Cannata F, Malvolti ME (2011) Long-term human impacts on genetic structure of Italian walnut inferred by SSR markers. Tree Genet Genomes 7:707–723

    Article  Google Scholar 

  • Porebski S, Bailey LG, Baum B (1997) Modification of a CTAB DNA extraction protocol for plants containing high polysaccharide and polyphenol components. Plant Mol Biol Rep 15:8–15

    Article  CAS  Google Scholar 

  • Prieto JA, Patiño OJ, Delgado WA, Moreno JP, Cuca LE (2011) Chemical composition, insecticidal, and antifungal activities of fruit essential oils of three Colombian Zanthoxylum species. Chil J Agric Res 71:73–82

  • Sun XW, Duan ZX (1996) Progress in the studies on medicinal plants of the genus Zanthoxylum Linn. Acta Pharm Sin 31:231–240

    CAS  Google Scholar 

  • Talontsi FM, Matasyoh JC, Ngoumfo RM, Chepkorir R (2011) Mosquito larvicidal activity of alkaloids from Zanthoxylum lemairei against the malaria vector Anopheles gambiae. Pestic Biochem Phys 99:82–85

    Article  CAS  Google Scholar 

  • Tantapakul C, Phakhodee W, Ritthiwigrom T, Yossathera K, Deachathai S, Laphookhieo S (2012) Antibacterial compounds from Zanthoxylum rhetsa. Arch Pharm Res 35:1139–1142

    Article  CAS  PubMed  Google Scholar 

  • Tu YL, Wei CS, Zuo ZL, Lu YM (2001) A new Zanthoxylum genus—Z. planipinum var. dingtanensis and the research of its species classification. Guizhou Sci 19:77–80

    Google Scholar 

  • Uzun A, Yesiloglu T, Tuzcu O, Gulsen O (2009) Genetic diversity and relationships within Citrus and related genera based on sequence related amplified polymorphism markers (SRAPs). Sci Hortic 121:306–312

    Article  CAS  Google Scholar 

  • Uzun A, Gulsen O, Seday U, Bircan M, Yilmaz KU (2010) SRAP based genetic analysis of some apricot cultivars. Rom Biotech Lett 15:5396–5404

    Google Scholar 

  • Xie DY, Chen QY (2013) Utilization of Chinese prickly ash in ancient Chinese people’s Diet. J Chuxiong Normal Univ 28:10–13

    Google Scholar 

  • Yin YG, Liu Y, Li HM, Zhao S, Wang SX, Liu Y, Wu D, Xu F (2014) Genetic diversity of Pleurotus pulmonarius revealed by RAPD, ISSR, and SRAP fingerprinting. Curr Microbiol 68:397–403

    Article  CAS  PubMed  Google Scholar 

  • Yoruk B, Taskin V (2014) Genetic diversity and relationships of wild and cultivated olives in Turkey. Plant Syst Evol 300:1247–1258

    Article  Google Scholar 

  • Yoshida T, Nagai H, Yahara T, Tachida H (2010) Genetic structure and putative selective sweep in the pioneer tree, Zanthoxylum ailanthoides. J Plant Res 123:607–616

    Article  PubMed  Google Scholar 

  • Yu J, Jing Z, Cheng J (2013) Genetic diversity and population structure of Stipa bungeana, an endemic species in Loess Plateau of China, revealed using combined ISSR and SRAP markers. Genet Mol Res 13:1097–1108

    Article  Google Scholar 

  • Zhang F, Ge YY, Wang WY, Shen XL, Liu XJ, Liu JX, Tian DQ, Yu XY (2012) Genetic diversity and population structure of cultivated bromeliad accessions assessed by SRAP markers. Sci Hortic 141:1–6

    Article  CAS  Google Scholar 

  • Zheng HX, Li ZQ, Xue HD, Wang DW, Sun Y (2011) RAPD analysis of the germplasm resources of Zanthoxylum bungeanum. J Northwest For Univ 26:96–100

    Google Scholar 

Download references

Acknowledgments

This work was financially supported by Special Fund for Forestry Research in the Public Interest (No.: 201304706) and Medicinal Plant Resources Nursery Construction and Improved Variety of Zanthoxylum (Qian ZY [2012] no.3002).

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Anzhi Wei.

Electronic supplementary material

Below is the link to the electronic supplementary material.

Supplementary material 1 (DOCX 46 kb)

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Feng, S., Yang, T., Liu, Z. et al. Genetic diversity and relationships of wild and cultivated Zanthoxylum germplasms based on sequence-related amplified polymorphism (SRAP) markers. Genet Resour Crop Evol 62, 1193–1204 (2015). https://doi.org/10.1007/s10722-015-0222-x

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s10722-015-0222-x

Keywords

Navigation