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PCR amplification of SNP loci from crude DNA for large-scale genotyping of oomycetes.

Identifieur interne : 000F51 ( Main/Exploration ); précédent : 000F50; suivant : 000F52

PCR amplification of SNP loci from crude DNA for large-scale genotyping of oomycetes.

Auteurs : Jian Hu [États-Unis] ; Rebecca Lyon [États-Unis] ; Yuxin Zhou [États-Unis] ; Kurt Lamour [États-Unis]

Source :

RBID : pubmed:24871597

Descripteurs français

English descriptors

Abstract

Similar to other eukaryotes, single nucleotide polymorphism (SNP) markers are abundant in many oomycete plant pathogen genomes. High resolution DNA melting analysis (HR-DMA) is a cost-effective method for SNP genotyping, but like many SNP marker technologies, is limited by the amount and quality of template DNA. We describe PCR preamplification of Phytophthora and Peronospora SNP loci from crude DNA extracted from a small amount of mycelium and/or infected plant tissue to produce sufficient template to genotype at least 10 000 SNPs. The approach is fast, inexpensive, requires minimal biological material and should be useful for many organisms in a variety of contexts.

DOI: 10.3852/13-218
PubMed: 24871597


Affiliations:


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Le document en format XML

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<div type="abstract" xml:lang="en">Similar to other eukaryotes, single nucleotide polymorphism (SNP) markers are abundant in many oomycete plant pathogen genomes. High resolution DNA melting analysis (HR-DMA) is a cost-effective method for SNP genotyping, but like many SNP marker technologies, is limited by the amount and quality of template DNA. We describe PCR preamplification of Phytophthora and Peronospora SNP loci from crude DNA extracted from a small amount of mycelium and/or infected plant tissue to produce sufficient template to genotype at least 10 000 SNPs. The approach is fast, inexpensive, requires minimal biological material and should be useful for many organisms in a variety of contexts. </div>
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