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1.
PLoS One ; 7(3): e32703, 2012.
Artigo em Inglês | MEDLINE | ID: mdl-22427867

RESUMO

Sheath blight (ShB) caused by the soil-borne pathogen Rhizoctonia solani is one of the most devastating diseases in rice world-wide. Global attention has focused on examining individual mapping populations for quantitative trait loci (QTLs) for ShB resistance, but to date no study has taken advantage of association mapping to examine hundreds of lines for potentially novel QTLs. Our objective was to identify ShB QTLs via association mapping in rice using 217 sub-core entries from the USDA rice core collection, which were phenotyped with a micro-chamber screening method and genotyped with 155 genome-wide markers. Structure analysis divided the mapping panel into five groups, and model comparison revealed that PCA5 with genomic control was the best model for association mapping of ShB. Ten marker loci on seven chromosomes were significantly associated with response to the ShB pathogen. Among multiple alleles in each identified loci, the allele contributing the greatest effect to ShB resistance was named the putative resistant allele. Among 217 entries, entry GSOR 310389 contained the most putative resistant alleles, eight out of ten. The number of putative resistant alleles presented in an entry was highly and significantly correlated with the decrease of ShB rating (r = -0.535) or the increase of ShB resistance. Majority of the resistant entries that contained a large number of the putative resistant alleles belonged to indica, which is consistent with a general observation that most ShB resistant accessions are of indica origin. These findings demonstrate the potential to improve breeding efficiency by using marker-assisted selection to pyramid putative resistant alleles from various loci in a cultivar for enhanced ShB resistance in rice.


Assuntos
Resistência à Doença/genética , Oryza/genética , Doenças das Plantas/microbiologia , Rhizoctonia , Mapeamento Cromossômico , Genótipo , Desequilíbrio de Ligação , Modelos Genéticos , Oryza/microbiologia , Análise de Componente Principal , Locos de Características Quantitativas/genética
2.
PLoS One ; 7(12): e52540, 2012.
Artigo em Inglês | MEDLINE | ID: mdl-23285082

RESUMO

Straighthead, a physiological disorder characterized by sterile florets and distorted spikelets, causes significant yield losses in rice, and occurs in many countries. The current control method of draining paddies early in the season stresses plants, is costly, and wastes water. Development of resistant cultivar is regarded as the most efficient way for its control. We mapped a QTL for straighthead resistance using two recombinant inbred line (RIL) F(9) populations that were phenotyped over two years using monosodium methanearsonate (MSMA) to induce the symptoms. One population of 170 RILs was genotyped with 136 SSRs and the other population of 91 RILs was genotyped with 159 SSRs. A major QTL qSH-8 was identified in an overlapping region in both populations, and explained 46% of total variation in one and 67% in another population for straighthead resistance. qSH-8 was fine mapped from 1.0 Mbp to 340 kb using 7 SSR markers and further mapped to 290 kb in a population between RM22573 and InDel 27 using 4 InDel markers. SSR AP3858-1 and InDel 11 were within the fine mapped region, and co-segregated with straighthead resistance in both RIL populations, as well as in a collection of diverse global accessions. These results demonstrate that AP3858-1 and InDel 11 can be used for marker-assisted selection (MAS) for straighthead resistant cultivars, which is especially important because there is no effective way to directly evaluate straighthead resistance.


Assuntos
Resistência à Doença/genética , Ligação Genética , Oryza/genética , Oryza/imunologia , Mapeamento Físico do Cromossomo , Doenças das Plantas/genética , Doenças das Plantas/imunologia , Cromossomos de Plantas/genética , Cruzamentos Genéticos , Marcadores Genéticos , Genótipo , Mutação INDEL/genética , Endogamia , Repetições de Microssatélites/genética , Fenótipo , Polimorfismo Genético , Locos de Características Quantitativas/genética , Recombinação Genética/genética , Reprodutibilidade dos Testes
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