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ISSR and DAMD markers revealed high genetic variability within Flavoparmelia caperata in Western Himalaya (India)

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Abstract

Flavoparmelia caperata (L.) Hale is medicinally very important and possesses antifungal and antibacterial activities. F. caperata is the only species found in India. Inter simple sequence repeat (ISSR) and Directed amplification of minisatellite DNA (DAMD) methods were used to analyze the genetic variability within F. caperata from the Western Himalayan region of India. Eleven ISSR and 10 DAMD primers produced 139 and 117 polymorphic bands, and detected 91.44 and 82.34 % polymorphisms, respectively. Cumulative band data generated for ISSR and DAMD markers resulted in 86.86 % polymorphism across all the accessions of F. caperata. The average Polymorphic information content (PIC) value obtained with ISSR, DAMD, and cumulative band data were 0.28, 0.27, and 0.27, respectively. The clustering of the F. caperata accessions in the UPGMA dendrogram showed that these accessions are intermingled with each other in different subclusters irrespective of their geographical affiliations. The pattern of genetic variations within F. caperata accessions could be due to free exchange of spores that might have taken place among these accessions in the wild. ISSR and DAMD markers efficiently and reliably resulted in discrete banding patterns and polymorphic profiles. These markers despite targeting different regions of genome, revealed almost similar levels of polymorphism across all the accessions. The wide range of genetic distance and high level of polymorphism detected by ISSR and DAMD reflected a high genetic variability among the different accessions of F. caperata.

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References

  • Bayraktar H, Dolar FS, Maden S (2008) Use of RAPD and ISSR markers in detection of genetic variation and population structure among Fusarium oxysporum f. sp. ciceris isolates on chickpea. Turk J Phytopathol 156:146–154

    Article  CAS  Google Scholar 

  • Botstein D, White RL, Skolnick M, Davis RW (1980) Construction of a genetic linkage map in man using restriction fragment length polymorphism. Am J Hum Genet 32:314–331

    PubMed  CAS  PubMed Central  Google Scholar 

  • Cobanoglu G, Sesal C, Gokmen B, Cakar S (2010) Evaluation of the antimicrobial properties of some lichens. SW J Hort Biol Environ 1:153–158

    Google Scholar 

  • Crespo A, Kauff F, Divakar PK et al (2010) Phylogenetic generic classification of parmelioid lichens (Parmeliaceae, Ascomycota) based on molecular, morphological and chemical evidence. Taxon 59:1735–1753

    Google Scholar 

  • Fontaine KM, Stocker-Worgotter ET, Booth T, Piercey-Normore MD (2013) Genetic diversity of the lichen-forming alga, Diplosphaera chodatii, in North America and Europe. Lichenologist 45(6):799–813

    Article  Google Scholar 

  • Frankham R (1996) Relationship of genetic variation to population size in wildlife. Conserv Biol 10:1500–1508

    Article  Google Scholar 

  • Frankham R (1999) Quantitative genetics in conservation biology. Genet Res 74:237–244

    Article  PubMed  CAS  Google Scholar 

  • Grube M, Hawksworth DL (2007) Trouble with lichen: the re-evaluation and re-interpretation of thallus form and fruit body types in the molecular era. Mycol Res 111:1116–1132

    Article  PubMed  Google Scholar 

  • Hamada H, Kakunaga T (1982) Potential Z-DNA forming sequences are highly dispersed in the human genome. Nature 298:396–398

    Article  PubMed  CAS  Google Scholar 

  • Heath DD, Iwama GK, Devlin RH (1993) PCR primed with the VNTR core sequences yields species specific patterns and hypervariable probes. Nucleic Acids Res 21:5782–5785

    Article  PubMed  CAS  PubMed Central  Google Scholar 

  • Honegger R, Zipper U, Scherrer, Dyer PS (2004) Genetic diversity in Xanthoria parietina (L.) Th. Fr. (Lichen-forming ascomycete) from worldwide locations. Lichenologist 36(6):381–390

    Article  Google Scholar 

  • Lande R (1988) Genetics and demography in biological. Conserv Sci 241:1455–1460

    CAS  Google Scholar 

  • Mantel N (1967) The detection of disease clustering and a generalized regression approach. Cancer Res 27:209–220

    PubMed  CAS  Google Scholar 

  • Murtagh GJ, Dyer PS, McClure PC, Crittenden PD (1999) Use of randomly amplified polymorphic DNA markers as a tool to study variation in lichen-forming fungi. Lichenologist 31(3):257–267

    Article  Google Scholar 

  • Nash TH III, Ryan BD, Gries C, Bungartz F (2002) Lichen flora of the greater sonoran desert region, vol I. Lichens Unlimited, Arizona State University, Tempe

    Google Scholar 

  • Page RDM (2001) TreeView (Win32), Ver. 1.6.5. Available from: http://taxonomy.zoology.gla.ac.uk/rod/treeview.html

  • Pavlicek A, Hrda S, Flegr J (1999) Free Tree—freeware program for construction of phylogenetic trees on the basis of distance data and bootstrapping/ jackknife analysis of the tree robustness. Application in the RAPD analysis of the genus Frenkelia. Folia Biol (Praha) 45:97–99, Available from: http://www.natur.cuni.cz/~flegr/programs/freetree.htm

    CAS  Google Scholar 

  • Pennington CW (1963) The Tarahumar of Mexico: their environment and material culture. Univ of Utah Press, Salt Lake City

    Google Scholar 

  • Printzen C (2002) Fungal specific primers for PCR-amplification of mitochondrial LSU in lichens. Mol Ecol Notes 2:130–132

    Article  CAS  Google Scholar 

  • Provost A, Wilkinson MJ (1999) A new system of comparing PCR primers applied to ISSR fingerprinting of potato cultivars. Theor Appl Genet 98:107–112

    Article  Google Scholar 

  • Rohlf FJ (1998) NTSYS-pc: numerical taxonomy and multivariate analysis system, version 2.02e. Applied Biostatistics Inc., Exeter Software, Setauket

    Google Scholar 

  • Shah A, Li DZ, Gao LM, Li HT, Möller M (2008) Genetic diversity within and among populations of the endangered species Taxus fauna (Taxaceae) from Pakistan and implications for its conservation. Biochem Syst Ecol 36:183–193

    Article  CAS  Google Scholar 

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

    Article  PubMed  CAS  PubMed Central  Google Scholar 

  • Uphof JCT (1959) Dictionary of economic plants. Hafner, New York

    Google Scholar 

  • Yuzbasioglu E, Halici MG, Karabacak M, Aksoy A (2011) RAPD and ISSR markers indicate high genetic variation within Lobathallia radiosa in Turkey. Mycol Prog 10:219–228

    Article  Google Scholar 

  • Zhou Z, Bebeli PJ, Somers DJ, Gustafson JP (1997) Direct amplification of minisatellite-region DNA with VNTR core sequences in the genus Oryza. Theor Appl Genet 95:942–949

    Article  CAS  Google Scholar 

  • Zietkiewicz E, Rafalski A, Labuda D (1994) Genome fingerprinting by simple sequence repeat (SSR)-anchored polymerase chain reaction amplification. Genomics 20:176–183

    Article  PubMed  CAS  Google Scholar 

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Acknowledgments

The authors are thankful to the Director of the CSIR-National Botanical Research Institute, Lucknow for faculties and encouragements. The financial support (No. BT/PR1457/39/204/2011) received from the Department of Biotechnology, New Delhi is gratefully acknowledged.

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Correspondence to T. S. Rana.

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Singh, N., Bajpai, R., Mahar, K.S. et al. ISSR and DAMD markers revealed high genetic variability within Flavoparmelia caperata in Western Himalaya (India). Physiol Mol Biol Plants 20, 501–508 (2014). https://doi.org/10.1007/s12298-014-0256-0

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