Mapping of Ascochyta blight resistance gene(s)/QTLs from exotic Cicer arietinum L. germplasm in cultivated kabuli chickpea
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Date
2019
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Punjab Agricultural University, Ludhiana
Abstract
Chickpea is an important pulse crop in the world after dry beans. Ascochyta blight caused by Ascochyta rabiei is a major fungal disease of chickpea and can cause upto 100% yield losses under favourable conditions. It is both air-borne and seed-borne disease that spreads rapidly to all the aerial parts including leaves, petioles, flowers, pods, branches and stems leading to rapid collapse and death of plants. The present investigation was undertaken for mapping of Ascochyta blight resistance gene using an interspecific population. The chickpea cultivar, L 552, besides having several agronomically important characters is susceptible to Ascochyta blight and the exotic accession, FLIP 05-43, is resistant to Ascochyta blight. An F2 interspecific population was developed from cross between L 552 (female parent) and FLIP 05-43 (donar parent). Inheritance studies in F2 and F2:3 populations revealed that inheritance of Ascochyta blight resistance was controlled by monogenic recessive gene, that was designated as arr6. A total of 300 SSR markers were used for polymorphism survey of the parents. A considerably low polymorphism of 15.30 % was found between the parents, and 46 polymorphic markers were used for genotyping of F2 population. For generating linkage map, these 46 SSRs were subjected to linkage analysis using MAPDISTO (1.7.6.5) software at LOD of 3, only 31 markers were mapped generating a linkage map of 377.14 cM with eight linkage groups. Using this linkage map, arr6 gene was mapped onto linkage group 4 at a distance of 8.6 cM distal to CGMM072 marker and from NCPGR247 marker, it was located at a distance 16.1 cM. There is a need to identify more SSR markers in the region lying between the markers CGMM072 and NCPGR247 in order to minimize the distance from the arr6 gene and its transfer to the elite cultivar (L 552) for providing durable resistance against Ascochyta blight. Thus, this study provides further prospective for fine mapping and map based cloning of the arr6 gene.
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