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Using SNP markers to dissect linkage disequilibrium at a major quantitative trait locus for resistance to the potato cyst nematode Globodera pallida on potato chromosome V.

Identifieur interne : 001A18 ( Main/Exploration ); précédent : 001A17; suivant : 001A19

Using SNP markers to dissect linkage disequilibrium at a major quantitative trait locus for resistance to the potato cyst nematode Globodera pallida on potato chromosome V.

Auteurs : Ute Achenbach [Allemagne] ; Joao Paulo ; Evgenyia Ilarionova ; Jens Lübeck ; Josef Strahwald ; Eckhard Tacke ; Hans-Reinhard Hofferbert ; Christiane Gebhardt

Source :

RBID : pubmed:19020852

Descripteurs français

English descriptors

Abstract

The damage caused by the parasitic root cyst nematode Globodera pallida is a major yield-limiting factor in potato cultivation . Breeding for resistance is facilitated by the PCR-based marker 'HC', which is diagnostic for an allele conferring high resistance against G. pallida pathotype Pa2/3 that has been introgressed from the wild potato species Solanum vernei into the Solanum tuberosum tetraploid breeding pool. The major quantitative trait locus (QTL) controlling this nematode resistance maps on potato chromosome V in a hot spot for resistance to various pathogens including nematodes and the oomycete Phytophthora infestans. An unstructured sample of 79 tetraploid, highly heterozygous varieties and breeding clones was selected based on presence (41 genotypes) or absence (38 genotypes) of the HC marker. Testing the clones for resistance to G. pallida confirmed the diagnostic power of the HC marker. The 79 individuals were genotyped for 100 single nucleotide polymorphisms (SNPs) at 10 loci distributed over 38 cM on chromosome V. Forty-five SNPs at six loci spanning 2 cM in the interval between markers GP21-GP179 were associated with resistance to G. pallida. Based on linkage disequilibrium (LD) between SNP markers, six LD groups comprising between 2 and 18 SNPs were identified. The LD groups indicated the existence of multiple alleles at a single resistance locus or at several, physically linked resistance loci. LD group C comprising 18 SNPs corresponded to the 'HC' marker. LD group E included 16 SNPs and showed an association peak, which positioned one nematode resistance locus physically close to the R1 gene family.

DOI: 10.1007/s00122-008-0925-x
PubMed: 19020852


Affiliations:


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Le document en format XML

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<term>Genotype (MeSH)</term>
<term>Immunity, Innate (genetics)</term>
<term>Linkage Disequilibrium (MeSH)</term>
<term>Plant Diseases (genetics)</term>
<term>Plant Diseases (parasitology)</term>
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<term>Polymorphism, Single Nucleotide (MeSH)</term>
<term>Quantitative Trait Loci (MeSH)</term>
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<term>Solanum tuberosum (parasitology)</term>
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<term>Locus de caractère quantitatif (MeSH)</term>
<term>Maladies des plantes (génétique)</term>
<term>Maladies des plantes (parasitologie)</term>
<term>Marqueurs génétiques (MeSH)</term>
<term>Polymorphisme de nucléotide simple (MeSH)</term>
<term>Réaction de polymérisation en chaîne (MeSH)</term>
<term>Solanum tuberosum (génétique)</term>
<term>Solanum tuberosum (parasitologie)</term>
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<div type="abstract" xml:lang="en">The damage caused by the parasitic root cyst nematode Globodera pallida is a major yield-limiting factor in potato cultivation . Breeding for resistance is facilitated by the PCR-based marker 'HC', which is diagnostic for an allele conferring high resistance against G. pallida pathotype Pa2/3 that has been introgressed from the wild potato species Solanum vernei into the Solanum tuberosum tetraploid breeding pool. The major quantitative trait locus (QTL) controlling this nematode resistance maps on potato chromosome V in a hot spot for resistance to various pathogens including nematodes and the oomycete Phytophthora infestans. An unstructured sample of 79 tetraploid, highly heterozygous varieties and breeding clones was selected based on presence (41 genotypes) or absence (38 genotypes) of the HC marker. Testing the clones for resistance to G. pallida confirmed the diagnostic power of the HC marker. The 79 individuals were genotyped for 100 single nucleotide polymorphisms (SNPs) at 10 loci distributed over 38 cM on chromosome V. Forty-five SNPs at six loci spanning 2 cM in the interval between markers GP21-GP179 were associated with resistance to G. pallida. Based on linkage disequilibrium (LD) between SNP markers, six LD groups comprising between 2 and 18 SNPs were identified. The LD groups indicated the existence of multiple alleles at a single resistance locus or at several, physically linked resistance loci. LD group C comprising 18 SNPs corresponded to the 'HC' marker. LD group E included 16 SNPs and showed an association peak, which positioned one nematode resistance locus physically close to the R1 gene family.</div>
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<AbstractText>The damage caused by the parasitic root cyst nematode Globodera pallida is a major yield-limiting factor in potato cultivation . Breeding for resistance is facilitated by the PCR-based marker 'HC', which is diagnostic for an allele conferring high resistance against G. pallida pathotype Pa2/3 that has been introgressed from the wild potato species Solanum vernei into the Solanum tuberosum tetraploid breeding pool. The major quantitative trait locus (QTL) controlling this nematode resistance maps on potato chromosome V in a hot spot for resistance to various pathogens including nematodes and the oomycete Phytophthora infestans. An unstructured sample of 79 tetraploid, highly heterozygous varieties and breeding clones was selected based on presence (41 genotypes) or absence (38 genotypes) of the HC marker. Testing the clones for resistance to G. pallida confirmed the diagnostic power of the HC marker. The 79 individuals were genotyped for 100 single nucleotide polymorphisms (SNPs) at 10 loci distributed over 38 cM on chromosome V. Forty-five SNPs at six loci spanning 2 cM in the interval between markers GP21-GP179 were associated with resistance to G. pallida. Based on linkage disequilibrium (LD) between SNP markers, six LD groups comprising between 2 and 18 SNPs were identified. The LD groups indicated the existence of multiple alleles at a single resistance locus or at several, physically linked resistance loci. LD group C comprising 18 SNPs corresponded to the 'HC' marker. LD group E included 16 SNPs and showed an association peak, which positioned one nematode resistance locus physically close to the R1 gene family.</AbstractText>
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<li>Cologne</li>
</settlement>
</list>
<tree>
<noCountry>
<name sortKey="Gebhardt, Christiane" sort="Gebhardt, Christiane" uniqKey="Gebhardt C" first="Christiane" last="Gebhardt">Christiane Gebhardt</name>
<name sortKey="Hofferbert, Hans Reinhard" sort="Hofferbert, Hans Reinhard" uniqKey="Hofferbert H" first="Hans-Reinhard" last="Hofferbert">Hans-Reinhard Hofferbert</name>
<name sortKey="Ilarionova, Evgenyia" sort="Ilarionova, Evgenyia" uniqKey="Ilarionova E" first="Evgenyia" last="Ilarionova">Evgenyia Ilarionova</name>
<name sortKey="Lubeck, Jens" sort="Lubeck, Jens" uniqKey="Lubeck J" first="Jens" last="Lübeck">Jens Lübeck</name>
<name sortKey="Paulo, Joao" sort="Paulo, Joao" uniqKey="Paulo J" first="Joao" last="Paulo">Joao Paulo</name>
<name sortKey="Strahwald, Josef" sort="Strahwald, Josef" uniqKey="Strahwald J" first="Josef" last="Strahwald">Josef Strahwald</name>
<name sortKey="Tacke, Eckhard" sort="Tacke, Eckhard" uniqKey="Tacke E" first="Eckhard" last="Tacke">Eckhard Tacke</name>
</noCountry>
<country name="Allemagne">
<region name="Rhénanie-du-Nord-Westphalie">
<name sortKey="Achenbach, Ute" sort="Achenbach, Ute" uniqKey="Achenbach U" first="Ute" last="Achenbach">Ute Achenbach</name>
</region>
</country>
</tree>
</affiliations>
</record>

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