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Leaf Tissue Sampling and DNA Extraction Protocols

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Book cover Molecular Plant Taxonomy

Part of the book series: Methods in Molecular Biology ((MIMB,volume 1115))

Abstract

Taxonomists must be familiar with a number of issues in collecting and transporting samples using freezing methods (liquid nitrogen and dry ice), desiccants (silica gel and blotter paper), and preservatives (CTAB, ethanol, and isopropanol), with each method having its own merits and limitations. For most molecular studies, a reasonably good quality and quantity of DNA is required, which can only be obtained using standard DNA extraction protocols. There are many DNA extraction protocols that vary from simple and quick ones that yield low-quality DNA but good enough for routine analyses to the laborious and time-consuming standard methods that usually produce high quality and quantities of DNA. The protocol to be chosen will depend on the quality and quantity of DNA needed, the nature of samples, and the presence of natural substances that may interfere with the extraction and subsequent analysis. The protocol described in this chapter has been tested for extracting DNA from eight species and provided very good quality and quantity of DNA for different applications, including those genotyping methods that use restriction enzymes.

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References

  1. Klimyuk VI, Carroll BJ, Thomas CM, Jones JDG (1993) Alkali treatment for rapid preparation of plant material for reliable PCR analysis. Plant J 3:493–494

    Article  CAS  PubMed  Google Scholar 

  2. Clancy JA, Jitkov VA, Han F, Ullrich SE (1996) Barley tissue as direct template for PCR: a practical breeding tool. Mol Breed 2:181–183

    Article  CAS  Google Scholar 

  3. Langridge U, Schwall M, Langridge P (1991) Squashes of plant tissue as substrate for PCR. Nucleic Acids Res 19:6954

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  4. Ikeda N, Bautista NS, Yamada T, Kamijima O, Ishii T (2001) Ultra-simple DNA extraction method for marker-assisted selection using microsatellite markers in rice. Plant Mol Biol Report 19:27–32

    Article  CAS  Google Scholar 

  5. Lin JJ, Fleming R, Kuo JMBF, Saunders JA (2000) Detection of plant genes using a rapid, nonorganic DNA purification method. Biotechniques 28:346–350

    CAS  PubMed  Google Scholar 

  6. Gao S, Martinez C, Skinner DJ, Krivanek AF, Crouch JH, Xu Y (2008) Development of a seed DNA-based genotyping system for marker-assisted selection in maize. Mol Breed 22:477–494

    Article  CAS  Google Scholar 

  7. Marsal G, Baiges I, Canals JM, Zamora F, Fort F (2011) A fast, efficient method for extracting DNA from leaves, stems, and seeds of Vitis vinifera L. Am J Enol Vitic 62:376–381

    Article  CAS  Google Scholar 

  8. Praveen M, Nanna RS (2009) A simple and rapid method for DNA extraction from leaves of tomato, tobacco and rape seed. J Phytol 1:388–390

    Google Scholar 

  9. Salim K, Qureshi MI, Kamaluddin, Tanweer A, Abdin MZ (2007) Protocol for isolation of genomic DNA from dry and fresh roots of medicinal plants suitable for RAPD and restriction digestion. Afr J Biotechnol 6:175–178

    Google Scholar 

  10. Lin J, Ritland K (1995) Flower petals allow simpler and better isolation of DNA for plant RAPD analyses. Plant Mol Biol Report 13:210–213

    Article  CAS  Google Scholar 

  11. Reddy GM, Coe E (1990) Isolation of nucleic acids from pollen grains. Maize Genet Coop News Lett 1990, 43

    Google Scholar 

  12. Chase MW, Hills HH (1991) Silica gel: an ideal material for field preservation of leaf samples for DNA studies. Taxon 40:215–220

    Article  Google Scholar 

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

    CAS  PubMed Central  PubMed  Google Scholar 

  14. Elshire RJ, Glaubitz JC, Sun Q, Poland JA, Kawamoto K, Buckler ES et al (2011) A robust, simple genotyping-by-sequencing (GBS) approach for high diversity species. PLoS ONE 6:e19379

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  15. Rogstad SH (1992) Saturated NaCl-CTAB solution as a means of field preservation of leaves for DNA analyses. Taxon 41:701–708

    Article  Google Scholar 

  16. Storchova H, Hrdlickova R, Chrtek J Jr, Tetera M, Fitze D, Fehrer J (2000) An improved method of DNA isolation from plants collected in the field and conserved in saturated NaCl/CTAB solution. Taxon 49:79–84

    Article  Google Scholar 

  17. Fukatsu T (1999) Acetone preservation: a practical technique for molecular analysis. Mol Ecol 8:1935–1945

    Article  CAS  PubMed  Google Scholar 

  18. Flournoy LE, Adams RP, Pandy RN (1996) Interim and archival preservation of plant specimens in alcohols for DNA studies. Biotechniques 20:657–660

    CAS  PubMed  Google Scholar 

  19. Dubreuil P, Warburton M, Chastanet M, Hoisington D, Charcosset A (2006) More on the introduction of temperate maize into Europe: large-scale bulk SSR genotyping and new historical elements. Maydica 51:281–291

    Google Scholar 

  20. Warburton ML, Setimela P, Franco J, Cordova H, Pixley K, Banziger M et al (2010) Toward a cost-effective fingerprinting methodology to distinguish maize open-pollinated varieties. Crop Sci 50:467–477

    Article  Google Scholar 

  21. Etten JV, Lopez MRF, Monterroso LGM, Samayoa KMP (2008) Genetic diversity of maize (Zea mays L. ssp. mays) in communities of the western highlands of Guatemala: geographical patterns and processes. Genet Resour Crop Evol 55:303–317

    Article  Google Scholar 

  22. Eschholz TW, Peter R, Stamp P, Hund A (2008) Genetic diversity of Swiss maize (Zea mays L. ssp. mays) assessed with individuals and bulks on agarose gels. Genet Resour Crop Evol 55:971–983

    Article  Google Scholar 

  23. Reif JC, Hamrit S, Heckenberger M, Schipprack W, Peter MH, Bohn M et al (2005) Genetic structure and diversity of European flint maize populations determined with SSR analyses of individuals and bulks. Theor Appl Genet 111:906–913

    Article  CAS  PubMed  Google Scholar 

  24. Michelmore RW, Paran I, Kesseli RV (1991) Identification of markers linked to disease-resistance genes by bulked segregant analysis: a rapid method to detect markers in specific genomic regions by using segregating populations. Proc Natl Acad Sci USA 88:9828–9832

    Article  CAS  PubMed  Google Scholar 

  25. Pacek P, Sajantila A, Syvanen AC (1993) Determination of allele frequencies at loci with length polymorphism by quantitative analysis of DNA amplified from pooled samples. PCR Methods Appl 2:313–317

    Article  CAS  PubMed  Google Scholar 

  26. Fu YB (2003) Applications of bulking in molecular characterization of plant germplasm: a critical review. Plant Gen Res 1:161–167

    Article  Google Scholar 

  27. Wang H, Qi MQ, Cutler AJ (1993) A simple method of preparing plant samples for PCR. Nucleic Acids Res 21:4153–4154

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  28. Williams CE, Ronald PC (1994) PCR template-DNA isolated quickly from monocot and dicot leaves without tissue homogenization. Nucleic Acids Res 22:1917–1918

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  29. Post RV, Post LV, Dayteg C, Nilsson M, Forster BP, Tuvesson S (2003) A high-throughput DNA extraction method for barley seed. Euphytica 130:255–260

    Article  Google Scholar 

  30. Saghai-Maroof MA, Soliman KM, Jorgensen RA, Allard RW (1984) Ribosomal DNA spacer-length polymorphisms in barley: mendelian inheritance, chromosomal location, and population dynamics. Proc Natl Acad Sci 81:8014–8018

    Article  CAS  PubMed  Google Scholar 

  31. Murray MG, Thompson WF (1980) Rapid isolation of high molecular weight plant DNA. Nucleic Acids Res 8:4321–4325

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  32. Paterson AH, Brubaker CL, Wendel JF (1993) A rapid method for extraction of cotton (Gossypium spp.) genomic DNA suitable for RFLP or PCR analysis. Plant Mol Biol Report 11:122–127

    Article  CAS  Google Scholar 

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Acknowledgements

This protocol was optimized for the molecular breeding component of the Drought Tolerant Maize for Africa (DTMA) project, which is funded by funded by the Bill and Melinda Gates Foundation. The author would like to thank Veronica Ogugo for testing the protocol in different species.

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© 2014 Springer New York

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Semagn, K. (2014). Leaf Tissue Sampling and DNA Extraction Protocols. In: Besse, P. (eds) Molecular Plant Taxonomy. Methods in Molecular Biology, vol 1115. Humana Press, Totowa, NJ. https://doi.org/10.1007/978-1-62703-767-9_3

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  • DOI: https://doi.org/10.1007/978-1-62703-767-9_3

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  • Publisher Name: Humana Press, Totowa, NJ

  • Print ISBN: 978-1-62703-766-2

  • Online ISBN: 978-1-62703-767-9

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