Serveur d'exploration sur les maladies des plantes grimpantes

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Construction of a high-density linkage map and QTL detection of downy mildew resistance in Vitis aestivalis-derived 'Norton'.

Identifieur interne : 000186 ( Main/Exploration ); précédent : 000185; suivant : 000187

Construction of a high-density linkage map and QTL detection of downy mildew resistance in Vitis aestivalis-derived 'Norton'.

Auteurs : Surya Sapkota [États-Unis] ; Li-Ling Chen [États-Unis] ; Shanshan Yang [États-Unis] ; Katie E. Hyma [États-Unis] ; Lance Cadle-Davidson [États-Unis] ; Chin-Feng Hwang [États-Unis]

Source :

RBID : pubmed:30341491

Descripteurs français

English descriptors

Abstract

KEY MESSAGE

A major QTL for downy mildew resistance was detected on chromosome 18 (Rpv27) in Vitis aestivalis-derived 'Norton' based on a high-resolution linkage map with SNP and SSR markers as well as 2 years of field and laboratory phenotyping data. Grapevine downy mildew caused by the oomycete Plasmopara viticola is one of the most widespread and destructive diseases, particularly in humid viticultural areas where it damages green tissues and defoliates vines. Traditional Vitis vinifera wine grape cultivars are susceptible to downy mildew whereas several North American and a few Asian cultivars possess various levels of resistance to this disease. To identify genetic determinants of downy mildew resistance in V. aestivalis-derived 'Norton,' a mapping population with 182 genotypes was developed from a cross between 'Norton' and V. vinifera 'Cabernet Sauvignon' from which a consensus map was constructed via 411 simple sequence repeat (SSR) markers. Using genotyping-by-sequencing, 3825 single nucleotide polymorphism (SNP) markers were also generated. Of these, 1665 SNP and 407 SSR markers were clustered into 19 linkage groups in 159 genotypes, spanning a genetic distance of 2203.5 cM. Disease progression in response to P. viticola was studied in this population for 2 years under both laboratory and field conditions, and strong correlations were observed among data sets (Spearman correlation coefficient = 0.57-0.79). A quantitative trait loci (QTL) analysis indicated a resistance locus on chromosome 18, here named Rpv27, explaining 33.8% of the total phenotypic variation. Flanking markers closely linked with the trait can be further used for marker-assisted selection in the development of new cultivars with resistance to downy mildew.


DOI: 10.1007/s00122-018-3203-6
PubMed: 30341491


Affiliations:


Links toward previous steps (curation, corpus...)


Le document en format XML

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<term>Chromosome Mapping (MeSH)</term>
<term>Chromosomes, Plant (genetics)</term>
<term>Disease Resistance (genetics)</term>
<term>Genetic Linkage (MeSH)</term>
<term>Genotype (MeSH)</term>
<term>Microsatellite Repeats (MeSH)</term>
<term>Oomycetes (pathogenicity)</term>
<term>Phenotype (MeSH)</term>
<term>Plant Diseases (genetics)</term>
<term>Plant Diseases (microbiology)</term>
<term>Polymorphism, Single Nucleotide (MeSH)</term>
<term>Quantitative Trait Loci (MeSH)</term>
<term>Vitis (genetics)</term>
<term>Vitis (microbiology)</term>
</keywords>
<keywords scheme="KwdFr" xml:lang="fr">
<term>Cartographie chromosomique (MeSH)</term>
<term>Chromosomes de plante (génétique)</term>
<term>Génotype (MeSH)</term>
<term>Liaison génétique (MeSH)</term>
<term>Locus de caractère quantitatif (MeSH)</term>
<term>Maladies des plantes (génétique)</term>
<term>Maladies des plantes (microbiologie)</term>
<term>Oomycetes (pathogénicité)</term>
<term>Phénotype (MeSH)</term>
<term>Polymorphisme de nucléotide simple (MeSH)</term>
<term>Répétitions microsatellites (MeSH)</term>
<term>Résistance à la maladie (génétique)</term>
<term>Vitis (génétique)</term>
<term>Vitis (microbiologie)</term>
</keywords>
<keywords scheme="MESH" qualifier="genetics" xml:lang="en">
<term>Chromosomes, Plant</term>
<term>Disease Resistance</term>
<term>Plant Diseases</term>
<term>Vitis</term>
</keywords>
<keywords scheme="MESH" qualifier="génétique" xml:lang="fr">
<term>Chromosomes de plante</term>
<term>Maladies des plantes</term>
<term>Résistance à la maladie</term>
<term>Vitis</term>
</keywords>
<keywords scheme="MESH" qualifier="microbiologie" xml:lang="fr">
<term>Maladies des plantes</term>
<term>Vitis</term>
</keywords>
<keywords scheme="MESH" qualifier="microbiology" xml:lang="en">
<term>Plant Diseases</term>
<term>Vitis</term>
</keywords>
<keywords scheme="MESH" qualifier="pathogenicity" xml:lang="en">
<term>Oomycetes</term>
</keywords>
<keywords scheme="MESH" qualifier="pathogénicité" xml:lang="fr">
<term>Oomycetes</term>
</keywords>
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<term>Chromosome Mapping</term>
<term>Genetic Linkage</term>
<term>Genotype</term>
<term>Microsatellite Repeats</term>
<term>Phenotype</term>
<term>Polymorphism, Single Nucleotide</term>
<term>Quantitative Trait Loci</term>
</keywords>
<keywords scheme="MESH" xml:lang="fr">
<term>Cartographie chromosomique</term>
<term>Génotype</term>
<term>Liaison génétique</term>
<term>Locus de caractère quantitatif</term>
<term>Phénotype</term>
<term>Polymorphisme de nucléotide simple</term>
<term>Répétitions microsatellites</term>
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<b>KEY MESSAGE</b>
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<p>A major QTL for downy mildew resistance was detected on chromosome 18 (Rpv27) in Vitis aestivalis-derived 'Norton' based on a high-resolution linkage map with SNP and SSR markers as well as 2 years of field and laboratory phenotyping data. Grapevine downy mildew caused by the oomycete Plasmopara viticola is one of the most widespread and destructive diseases, particularly in humid viticultural areas where it damages green tissues and defoliates vines. Traditional Vitis vinifera wine grape cultivars are susceptible to downy mildew whereas several North American and a few Asian cultivars possess various levels of resistance to this disease. To identify genetic determinants of downy mildew resistance in V. aestivalis-derived 'Norton,' a mapping population with 182 genotypes was developed from a cross between 'Norton' and V. vinifera 'Cabernet Sauvignon' from which a consensus map was constructed via 411 simple sequence repeat (SSR) markers. Using genotyping-by-sequencing, 3825 single nucleotide polymorphism (SNP) markers were also generated. Of these, 1665 SNP and 407 SSR markers were clustered into 19 linkage groups in 159 genotypes, spanning a genetic distance of 2203.5 cM. Disease progression in response to P. viticola was studied in this population for 2 years under both laboratory and field conditions, and strong correlations were observed among data sets (Spearman correlation coefficient = 0.57-0.79). A quantitative trait loci (QTL) analysis indicated a resistance locus on chromosome 18, here named Rpv27, explaining 33.8% of the total phenotypic variation. Flanking markers closely linked with the trait can be further used for marker-assisted selection in the development of new cultivars with resistance to downy mildew.</p>
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<AbstractText Label="KEY MESSAGE" NlmCategory="UNASSIGNED">A major QTL for downy mildew resistance was detected on chromosome 18 (Rpv27) in Vitis aestivalis-derived 'Norton' based on a high-resolution linkage map with SNP and SSR markers as well as 2 years of field and laboratory phenotyping data. Grapevine downy mildew caused by the oomycete Plasmopara viticola is one of the most widespread and destructive diseases, particularly in humid viticultural areas where it damages green tissues and defoliates vines. Traditional Vitis vinifera wine grape cultivars are susceptible to downy mildew whereas several North American and a few Asian cultivars possess various levels of resistance to this disease. To identify genetic determinants of downy mildew resistance in V. aestivalis-derived 'Norton,' a mapping population with 182 genotypes was developed from a cross between 'Norton' and V. vinifera 'Cabernet Sauvignon' from which a consensus map was constructed via 411 simple sequence repeat (SSR) markers. Using genotyping-by-sequencing, 3825 single nucleotide polymorphism (SNP) markers were also generated. Of these, 1665 SNP and 407 SSR markers were clustered into 19 linkage groups in 159 genotypes, spanning a genetic distance of 2203.5 cM. Disease progression in response to P. viticola was studied in this population for 2 years under both laboratory and field conditions, and strong correlations were observed among data sets (Spearman correlation coefficient = 0.57-0.79). A quantitative trait loci (QTL) analysis indicated a resistance locus on chromosome 18, here named Rpv27, explaining 33.8% of the total phenotypic variation. Flanking markers closely linked with the trait can be further used for marker-assisted selection in the development of new cultivars with resistance to downy mildew.</AbstractText>
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<Affiliation>Division of Plant Sciences, University of Missouri, Columbia, MO, 65211, USA.</Affiliation>
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<Affiliation>Plant Pathology and Plant Microbe Biology Section, School of Integrative Plant Science, NYS Agricultural Experiment Station, Cornell University, Geneva, NY, 14456, USA.</Affiliation>
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<Affiliation>Bioinformatics Core Facility, The Biodesign Institute, Arizona State University, Tempe, AZ, 85287-5001, USA.</Affiliation>
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<Affiliation>State Fruit Experiment Station at Mountain Grove Campus, Darr College of Agriculture, Missouri State University, Springfield, MO, 65897, USA. ChinFengHwang@MissouriState.edu.</Affiliation>
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<Grant>
<GrantID>Agriculture</GrantID>
<Agency>U.S. Department of Agriculture</Agency>
<Country></Country>
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<Grant>
<GrantID>Food Research Initiative (2013-67014-21360)</GrantID>
<Agency>U.S. Department of Agriculture</Agency>
<Country></Country>
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<Year>2018</Year>
<Month>10</Month>
<Day>19</Day>
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<QualifierName UI="Q000235" MajorTopicYN="N">genetics</QualifierName>
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<QualifierName UI="Q000235" MajorTopicYN="Y">genetics</QualifierName>
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<DescriptorName UI="D008040" MajorTopicYN="Y">Genetic Linkage</DescriptorName>
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<DescriptorName UI="D005838" MajorTopicYN="N">Genotype</DescriptorName>
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<MeshHeading>
<DescriptorName UI="D018895" MajorTopicYN="N">Microsatellite Repeats</DescriptorName>
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<MeshHeading>
<DescriptorName UI="D009868" MajorTopicYN="N">Oomycetes</DescriptorName>
<QualifierName UI="Q000472" MajorTopicYN="N">pathogenicity</QualifierName>
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<MeshHeading>
<DescriptorName UI="D010641" MajorTopicYN="N">Phenotype</DescriptorName>
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<MeshHeading>
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