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Crop Science Abstract - ORIGINAL RESEARCH

Development of SNP Assays for Marker-Assisted Selection of Two Southern Root-Knot Nematode Resistance QTL in Soybean


This article in CS

  1. Vol. 47 No. S2, p. S-73-S-82
    Received: Oct 15, 2006

    * Corresponding author(s): ha@uga.edu
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  1. Bo-Keun Ha *a,
  2. Richard S. Husseya and
  3. H. Roger Boermab
  1. a Dep. of Crop and Soil Sci., Univ. of Georgia, Center for Applied Genetic Technologies, 111 Riverbend Rd., Athens, GA 30602
    b Dep. of Plant Pathology, Univ. of Georgia, 2106 Miller Plant Sciences Bldg., Athens, GA 30602


The identification of single nucleotide polymorphism (SNP) markers tightly linked to soybean [Glycine max (L.) Merr.] quantitative trait loci (QTL) conditioning resistance to southern root-knot nematode (Meloidogyne incognita) (Mi) would enhance the efficiency and cost effectiveness of marker-assisted selection (MAS) for this trait. Bacterial artificial chromosome (BAC) ends and simple sequence repeat (SSR)-containing genomic DNA clones were used to develop SNP markers linked to two soybean Mi resistance QTL on Linkage Group O (LG-O) and LG-G. A total of 14 BAC-end sequences and seven SSR flanking regions were used to design primers to amplify genomic fragments of PI 96354 (Mi resistant) and ‘Bossier’ (Mi susceptible). We discovered three SNPs in Satt358 source-sequences located near a major Mi-resistant QTL on LG-O and three SNPs in Satt199 source-sequences located near a minor Mi-resistant QTL on LG-G. Using a direct hybridization SNP assay detected on a Luminex 100 flow cytometer, the SNP358 genotypes of 94 F2:3 lines from a cross of PI 96354 × Bossier were congruent with the genotypes of the SSR marker Satt358. The genotypes of SNP199 marker which targets a SNP in Satt199 source-sequence also showed 100% congruence with the genotypes of the SSR marker Satt199. SNP genotyping of 24 known Mi-resistant or Mi-susceptible cultivars showed that SNP358 and SNP199 markers should be highly effective in MAS for the Mi-resistance QTL on LG-O and LG-G.

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