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Genetic and cytogenetic mapping of DMI1, DMI2, and DMI3 genes of Medicago truncatula involved in Nod factor transduction, nodulation, and mycorrhization
- Source :
- Molecular Plant-Microbe Interactions 15 (2002) 11, Scopus-Elsevier, Molecular Plant-Microbe Interactions, 15(11), 1108-1118
- Publication Year :
- 2002
-
Abstract
- The DMI1, DMI2, and DMI3 genes of Medicago truncatula, which are required for both nodulation and mycorrhization, control early steps of Nod factor signal transduction. Here, we have used diverse approaches to pave the way for the map-based cloning of these genes. Molecular amplification fragment length polymorphism markers linked to the three genes were identified by bulked segregant analysis. Integration of these markers into the general genetic map of M. truncatula revealed that DMI1, DMI2, and DMI3 are located on linkage groups 2, 5, and 8, respectively. Cytogenetic studies using fluorescent in situ hybridization (FISH) on mitotic and pachytene chromThe DMI1, DMI2, and DMI3 genes of Medicago truncatula, which are required for both nodulation and mycorrhization, control early steps of Nod factor signal transduction. Here, we have used diverse approaches to pave the way for the map-based cloning of these genes. Molecular amplification fragment length polymorphism markers linked to the three genes were identified by bulked segregant analysis. Integration of these markers into the general genetic map of M. truncatula revealed that DMI1, DMI2, and DMI3 are located on linkage groups 2, 5, and 8, respectively. Cytogenetic studies using fluorescent in situ hybridization (FISH) on mitotic and pachytene chromosomes confirmed the location of DMI1, DMI2, and DMI3 on chromosomes 2, 5, and 8. FISH-pachytene studies revealed that the three genes are in euchromatic regions of the genome, with a ratio of genetic to cytogenetic distances between 0.8 and 1.6 cM per ¿m in the DMI1, DMI2, and DMI3 regions. Through grafting experiments, we showed that the genetic control of the dmi1, dmi2, and dmi3 nodulation phenotypes is determined at the root level. This means that mutants can be transformed by Agrobacterium rhizogenes to accelerate the complementation step of map-based cloning projects for DMI1, DMI2, and DMI3.
- Subjects :
- Genetic Markers
Chromosomes, Artificial, Bacterial
Physiology
Agrobacterium
extended dna fibers
markers
arabidopsis-thaliana
Biology
Genes, Plant
in-situ hybridization
Plant Roots
Genome
Chromosomes, Plant
Nod factor
resistance
Gene mapping
Gene Expression Regulation, Plant
Chromosome Segregation
Mycorrhizae
Medicago
Laboratorium voor Moleculaire Biologie
Symbiosis
Gene
In Situ Hybridization, Fluorescence
Genetics
fish
Genetic Complementation Test
Bulked segregant analysis
Chromosome Mapping
food and beverages
General Medicine
pea mutants
biology.organism_classification
Medicago truncatula
Phenotype
pachytene chromosomes
Genetic marker
Cytogenetic Analysis
identification
Laboratory of Molecular Biology
Agronomy and Crop Science
alfalfa
Polymorphism, Restriction Fragment Length
Rhizobium
Signal Transduction
Subjects
Details
- Language :
- English
- ISSN :
- 08940282
- Volume :
- 15
- Issue :
- 11
- Database :
- OpenAIRE
- Journal :
- Molecular Plant-Microbe Interactions
- Accession number :
- edsair.doi.dedup.....5ddd6ced675c50a64f4e4d3a36e4424b
- Full Text :
- https://doi.org/10.1094/mpmi.2002.15.11.1108