24 research outputs found

    Validation of a major QTL for salinity tolerance on chromosome 1 of rice in three different breeding populations

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    The effect of a major quantitative trait locus (QTL) for salinity tolerance in rice, designated as SalTol in a previous study, was tested using three F2 breeding populations. The populations were derived from the following F1 hybrids: 'BRRI dhan40' (susceptible)/ 'IR61920-3B-22-2-1' (highly tolerant); 'BRRI dhan28' (highly susceptible)/ 'IR50184-3B-18-2B-1' (moderately tolerant); and 'Kajalsail' (tolerant)/ 'IR52713-2B-8-2B-1-2' (tolerant). Targeted mapping of the chromosome region containing SolTol (49.6 to 87.1 cM) on chromosome 1 was conducted using 20 SSR and two EST markers. Comparisons of linkage maps of the three populations were very similar to the previous QTL map that identified SolTol. A QTL was only detected for 'BRRI dhan40'/ 'IR61920-3B-22-2-1' population. The SSR marker RM8094 was the most tightly-linked marker (P<0.001); four other markers, RM1287, RM3412, RM493 and CP03970, were also significantly associated with salinity tolerance (P<0.05). An F-3 population of the cross 'BRRI dhan40'/ 'IR61920' was used to reconfirm this result. This was interesting because the tolerant parent in this population was not related to the tolerant parent used for the original mapping population. QTLs were not detected at the SalTol locus for either of the other two populations. This was consistent with the phenotypes of the parents used to construct these populations, and indicates that the SolTol QTL may only be effective in specific populations

    QTL mapping for salinity tolerance of rice at seedline stage

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    A marker-assisted backcross approach for developing submergence-tolerant rice cultivars

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    Submergence stress regularly affects 15 million hectares or more of rainfed lowland rice areas in South and Southeast Asia. A major QTL on chromosome 9, Sub1, has provided the opportunity to apply marker assisted backcrossing (MAB) to develop submergence tolerant versions of rice cultivars that are widely grown in the region. In the present study, molecular markers that were tightly linked with Sub1, flanking Sub1, and unlinked to Sub1 were used to apply foreground, recombinant, and background selection, respectively, in backcrosses between a submergence-tolerant donor and the widely grown recurrent parent Swarna. By the BC2F2 generation a submergence tolerant plant was identified that possessed Swarna type simple sequence repeat (SSR) alleles on all fragments analyzed except the tip segment of rice chromosome 9 that possessed the Sub1 locus. A BC3F2 double recombinant plant was identified that was homozygous for all Swarna type alleles except for an approximately 2.3-3.4 Mb region surrounding the Sub1 locus. The results showed that the mega variety Swarna could be efficiently converted to a submergence tolerant variety in three backcross generations, involving a time of two to three years. Polymorphic markers for foreground and recombinant selection were identified for four other mega varieties to develop a wider range of submergence tolerant varieties to meet the needs of farmers in the flood-prone regions. This approach demonstrates the effective use of marker assisted selection for a major QTL in a molecular breeding program
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