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BAC-derived markers converted from RFLP linked to Phytophthora capsici resistance in pepper (Capsicum annuum L.).

Identifieur interne : 001D45 ( Main/Exploration ); précédent : 001D44; suivant : 001D46

BAC-derived markers converted from RFLP linked to Phytophthora capsici resistance in pepper (Capsicum annuum L.).

Auteurs : Hyoun-Joung Kim [Corée du Sud] ; Seok-Hyeon Nahm ; Heung-Ryul Lee ; Gi-Bo Yoon ; Ki-Taek Kim ; Byoung-Cheorl Kang ; Doil Choi ; Oh Yeol Kweon ; Myeong-Cheoul Cho ; Jin-Kyung Kwon ; Jung-Heon Han ; Jeong-Ho Kim ; Minkyu Park ; Jong Hwa Ahn ; Soon Ho Choi ; Nam Han Her ; Joo-Hee Sung ; Byung-Dong Kim

Source :

RBID : pubmed:18795251

Descripteurs français

English descriptors

Abstract

Phytophthora capsici Leonian, an oomycete pathogen, is a serious problem in pepper worldwide. Its resistance in pepper is controlled by quantitative trait loci (QTL). To detect QTL associated with P. capsici resistance, a molecular linkage map was constructed using 100 F(2) individuals from a cross between Capsicum annuum 'CM334' and C. annuum 'Chilsungcho'. This linkage map consisted of 202 restriction fragment length polymorphisms (RFLPs), 6 WRKYs and 1 simple sequence repeat (SSR) covering 1482.3 cM, with an average interval marker distance of 7.09 cM. QTL mapping of Phytophthora root rot and damping-off resistance was performed in F(2:3) originated from a cross between resistant Mexican landrace C. annuum 'CM334' and susceptible Korean landrace C. annuum 'Chilsungcho' using composite interval mapping (CIM) analysis. Four QTL explained 66.3% of the total phenotypic variations for root rot resistance and three 44.9% for damping-off resistance. Of these QTL loci, two were located close to RFLP markers CDI25 on chromosome 5 (P5) and CT211A on P9. A bacterial artificial chromosome (BAC) library from C. annuum 'CM334' was screened with these two RFLP probes to obtain sequence information around the RFLP marker loci for development of PCR-based markers. CDI25 and CT211 probes identified seven and eight BAC clones, respectively. Nine positive BAC clones containing probe regions were sequenced and used for cytogenetic analysis. One single-nucleotide amplified polymorphism (SNAP) for the CDI25 locus, and two SSRs and cleaved amplified polymorphic sequence (CAPS) for CT211 were developed using sequences of the positive BAC clones. These markers will be valuable for rapid selection of genotypes and map-based cloning for resistance genes against P. capsici.

DOI: 10.1007/s00122-008-0873-5
PubMed: 18795251


Affiliations:


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


Le document en format XML

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<term>Capsicum (genetics)</term>
<term>Capsicum (microbiology)</term>
<term>Chromosome Mapping (MeSH)</term>
<term>Chromosomes, Artificial, Bacterial (MeSH)</term>
<term>Chromosomes, Plant (MeSH)</term>
<term>DNA, Plant (genetics)</term>
<term>Genetic Markers (MeSH)</term>
<term>Genome, Plant (MeSH)</term>
<term>Immunity, Innate (MeSH)</term>
<term>Phytophthora (pathogenicity)</term>
<term>Plant Diseases (genetics)</term>
<term>Plant Diseases (microbiology)</term>
<term>Polymorphism, Restriction Fragment Length (MeSH)</term>
<term>Polymorphism, Single Nucleotide (MeSH)</term>
<term>Quantitative Trait Loci (MeSH)</term>
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<term>ADN des plantes (génétique)</term>
<term>Capsicum (génétique)</term>
<term>Capsicum (microbiologie)</term>
<term>Cartographie chromosomique (MeSH)</term>
<term>Chromosomes artificiels de bactérie (MeSH)</term>
<term>Chromosomes de plante (MeSH)</term>
<term>Génome végétal (MeSH)</term>
<term>Immunité innée (MeSH)</term>
<term>Locus de caractère quantitatif (MeSH)</term>
<term>Maladies des plantes (génétique)</term>
<term>Maladies des plantes (microbiologie)</term>
<term>Marqueurs génétiques (MeSH)</term>
<term>Phytophthora (pathogénicité)</term>
<term>Polymorphisme de nucléotide simple (MeSH)</term>
<term>Polymorphisme de restriction (MeSH)</term>
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<term>DNA, Plant</term>
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<term>Capsicum</term>
<term>Plant Diseases</term>
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<term>ADN des plantes</term>
<term>Capsicum</term>
<term>Maladies des plantes</term>
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<keywords scheme="MESH" qualifier="microbiologie" xml:lang="fr">
<term>Capsicum</term>
<term>Maladies des plantes</term>
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<keywords scheme="MESH" qualifier="microbiology" xml:lang="en">
<term>Capsicum</term>
<term>Plant Diseases</term>
</keywords>
<keywords scheme="MESH" qualifier="pathogenicity" xml:lang="en">
<term>Phytophthora</term>
</keywords>
<keywords scheme="MESH" qualifier="pathogénicité" xml:lang="fr">
<term>Phytophthora</term>
</keywords>
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<term>Chromosome Mapping</term>
<term>Chromosomes, Artificial, Bacterial</term>
<term>Chromosomes, Plant</term>
<term>Genetic Markers</term>
<term>Genome, Plant</term>
<term>Immunity, Innate</term>
<term>Polymorphism, Restriction Fragment Length</term>
<term>Polymorphism, Single Nucleotide</term>
<term>Quantitative Trait Loci</term>
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<term>Chromosomes artificiels de bactérie</term>
<term>Chromosomes de plante</term>
<term>Génome végétal</term>
<term>Immunité innée</term>
<term>Locus de caractère quantitatif</term>
<term>Marqueurs génétiques</term>
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<div type="abstract" xml:lang="en">Phytophthora capsici Leonian, an oomycete pathogen, is a serious problem in pepper worldwide. Its resistance in pepper is controlled by quantitative trait loci (QTL). To detect QTL associated with P. capsici resistance, a molecular linkage map was constructed using 100 F(2) individuals from a cross between Capsicum annuum 'CM334' and C. annuum 'Chilsungcho'. This linkage map consisted of 202 restriction fragment length polymorphisms (RFLPs), 6 WRKYs and 1 simple sequence repeat (SSR) covering 1482.3 cM, with an average interval marker distance of 7.09 cM. QTL mapping of Phytophthora root rot and damping-off resistance was performed in F(2:3) originated from a cross between resistant Mexican landrace C. annuum 'CM334' and susceptible Korean landrace C. annuum 'Chilsungcho' using composite interval mapping (CIM) analysis. Four QTL explained 66.3% of the total phenotypic variations for root rot resistance and three 44.9% for damping-off resistance. Of these QTL loci, two were located close to RFLP markers CDI25 on chromosome 5 (P5) and CT211A on P9. A bacterial artificial chromosome (BAC) library from C. annuum 'CM334' was screened with these two RFLP probes to obtain sequence information around the RFLP marker loci for development of PCR-based markers. CDI25 and CT211 probes identified seven and eight BAC clones, respectively. Nine positive BAC clones containing probe regions were sequenced and used for cytogenetic analysis. One single-nucleotide amplified polymorphism (SNAP) for the CDI25 locus, and two SSRs and cleaved amplified polymorphic sequence (CAPS) for CT211 were developed using sequences of the positive BAC clones. These markers will be valuable for rapid selection of genotypes and map-based cloning for resistance genes against P. capsici.</div>
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<AbstractText>Phytophthora capsici Leonian, an oomycete pathogen, is a serious problem in pepper worldwide. Its resistance in pepper is controlled by quantitative trait loci (QTL). To detect QTL associated with P. capsici resistance, a molecular linkage map was constructed using 100 F(2) individuals from a cross between Capsicum annuum 'CM334' and C. annuum 'Chilsungcho'. This linkage map consisted of 202 restriction fragment length polymorphisms (RFLPs), 6 WRKYs and 1 simple sequence repeat (SSR) covering 1482.3 cM, with an average interval marker distance of 7.09 cM. QTL mapping of Phytophthora root rot and damping-off resistance was performed in F(2:3) originated from a cross between resistant Mexican landrace C. annuum 'CM334' and susceptible Korean landrace C. annuum 'Chilsungcho' using composite interval mapping (CIM) analysis. Four QTL explained 66.3% of the total phenotypic variations for root rot resistance and three 44.9% for damping-off resistance. Of these QTL loci, two were located close to RFLP markers CDI25 on chromosome 5 (P5) and CT211A on P9. A bacterial artificial chromosome (BAC) library from C. annuum 'CM334' was screened with these two RFLP probes to obtain sequence information around the RFLP marker loci for development of PCR-based markers. CDI25 and CT211 probes identified seven and eight BAC clones, respectively. Nine positive BAC clones containing probe regions were sequenced and used for cytogenetic analysis. One single-nucleotide amplified polymorphism (SNAP) for the CDI25 locus, and two SSRs and cleaved amplified polymorphic sequence (CAPS) for CT211 were developed using sequences of the positive BAC clones. These markers will be valuable for rapid selection of genotypes and map-based cloning for resistance genes against P. capsici.</AbstractText>
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