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      Protocol: a simple method for extracting next-generation sequencing quality genomic DNA from recalcitrant plant species

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          Abstract

          Next-generation sequencing technologies rely on high quality DNA that is suitable for library preparation followed by sequencing. Some plant species store large amounts of phenolics and polysaccharides within their leaf tissue making genomic DNA extraction difficult. While many DNA extraction methods exist that contend with the presence of phenolics and polysaccharides, these methods rely on long incubations, multiple precipitations or commercially available kits to produce high molecular weight and contaminant-free DNA. In this protocol, we describe simple modifications to the established CTAB- based extraction method that allows for reliable isolation of high molecular weight genomic DNA from difficult to isolate plant species Corymbia (a eucalypt) and Coffea (coffee). The simplified protocol does not require multiple clean up steps or commercial based kits, and the isolated DNA passed stringent quality control standards for whole genome sequencing on Illumina HiSeq and TruSeq sequencing platforms.

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          Most cited references13

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          A quick and inexpensive method for removing polysaccharides from plant genomic DNA.

          A quick and inexpensive method has been demonstrated to remove polysaccharide contamination from plant DNA. Isolated plant genomic DNA with polysaccharide contaminants was dissolved in TE (10 mM Tris-HCl, pH 7.4, 1 mM EDTA) with NaCl ranging from 0.5-3.0 M, then precipitated with two volumes of ethanol. Most of the polysaccharides were removed effectively in a single high-salt precipitation at 1.0-2.5 M NaCl. At 3.0 M NaCl, the salt precipitated out of solution. Purified DNA was easily digested by either HindIII or EcoRI and was satisfactory as a template for PCR. The results show that high-salt precipitation effectively removed polysaccharides and their inhibitory effects on restriction enzyme and Taq polymerase activity.
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            An efficient method for isolation of RNA and DNA from plants containing polyphenolics.

            M. John (1992)
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              A simple and rapid method for isolation of high quality genomic DNA from fruit trees and conifers using PVP.

              Because DNA degradation is mediated by secondary plant products such as phenolic terpenoids, the isolation of high quality DNA from plants containing a high content of polyphenolics has been a difficult problem. We demonstrate an easy extraction process by modifying several existing ones. Using this process we have found it possible to isolate DNAs from four fruit trees, grape (Vitis spp.), apple (Malus spp.), pear (Pyrus spp.) and persimmon (Diospyros spp.) and four species of conifer, Pinus densiflora, Pinus koraiensis,Taxus cuspidata and Juniperus chinensis within a few hours. Compared with the existing method, we have isolated high quality intact DNAs (260/280 = 1.8-2.0) routinely yielding 250-500 ng/microl (total 7.5-15 microg DNA from four to five tissue discs).
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                Author and article information

                Contributors
                Journal
                Plant Methods
                Plant Methods
                Plant Methods
                BioMed Central
                1746-4811
                2014
                27 June 2014
                : 10
                : 21
                Affiliations
                [1 ]Queensland Alliance for Agriculture and Food Innovation, University of Queensland, Brisbane 4072, Australia
                Article
                1746-4811-10-21
                10.1186/1746-4811-10-21
                4105509
                25053969
                59281288-6ff1-47f7-a3a1-48062a922a7b
                Copyright © 2014 Healey et al.; licensee BioMed Central Ltd.

                This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver ( http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

                History
                : 7 May 2014
                : 23 June 2014
                Categories
                Methodology

                Plant science & Botany
                dna extraction,next-generation sequencing,ctab,corymbia,coffea
                Plant science & Botany
                dna extraction, next-generation sequencing, ctab, corymbia, coffea

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