Please use this identifier to cite or link to this item: http://223.31.159.10:8080/jspui/handle/123456789/497
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dc.contributor.authorDas, Shouvik-
dc.contributor.authorUpadhyaya, Hari D.-
dc.contributor.authorSrivastava, Rishi-
dc.contributor.authorBajaj, Deepak-
dc.contributor.authorGowda, C.L.L.-
dc.contributor.authorSharma, Shivali-
dc.contributor.authorSingh, Sube-
dc.contributor.authorTyagi, Akhilesh K.-
dc.contributor.authorParida, Swarup K.-
dc.date.accessioned2016-01-04T05:20:52Z-
dc.date.available2016-01-04T05:20:52Z-
dc.date.issued2015-
dc.identifier.citationDNA Res., 22(5): 377-386en_US
dc.identifier.issn1756-1663-
dc.identifier.urihttp://172.16.0.77:8080/jspui/handle/123456789/497-
dc.descriptionAccepted date: 25 August 2015en_US
dc.description.abstractWe developed 21,499 genome-wide insertion–deletion (InDel) markers (2- to 54-bp in silico fragment length polymorphism) by comparing the genomic sequences of four (desi, kabuli and wild C. reticulatum) chickpea [Cicer arietinum (L.)] accessions. InDel markers showing 2- to 6-bp fragment length polymorphism among accessions were abundant (76.8%) in the chickpea genome. The physically mapped 7,643 and 13,856 markers on eight chromosomes and unanchored scaffolds, respectively, were structurally and functionally annotated. The 4,506 coding (23% large-effect frameshift mutations) and regulatory InDel markers were identified from 3,228 genes (representing 11.7% of total 27,571 desi genes), suggesting their functional relevance for trait association/genetic mapping. High amplification (97%) and intra-specific polymorphic (60–83%) potential and wider genetic diversity (15–89%) were detected by genome-wide 6,254 InDel markers among desi, kabuli and wild accessions using even a simpler cost-effective agarose gel-based assay. This signifies added advantages of this user-friendly genetic marker system for manifold large-scale genotyping applications in laboratories with limited infrastructure and resources. Utilizing 6,254 InDel markers-based high-density (inter-marker distance: 0.212 cM) inter-specific genetic linkage map (ICC 4958 × ICC 17160) of chickpea as a reference, three major genomic regions harboring six flowering and maturity time robust QTLs (16.4–27.5% phenotypic variation explained, 8.1–11.5 logarithm of odds) were identified. Integration of genetic and physical maps at these target QTL intervals mapped on three chromosomes delineated five InDel markers-containing candidate genes tightly linked to the QTLs governing flowering and maturity time in chickpea. Taken together, our study demonstrated the practical utility of developing and high-throughput genotyping of such beneficial InDel markers at a genome-wide scale to expedite genomics-assisted breeding applications in chickpea.en_US
dc.description.sponsorshipThe authors gratefully acknowledge the financial support for this study provided by a research grant (102/IFD/SAN/2161/2013-14) from the Department of Biotechnology (DBT), Government of India. Funding to pay the Open Access publication charges for this article was provided by the National Institute of Plant Genome Research (NIPGR).en_US
dc.language.isoen_USen_US
dc.publisherOxford University Pressen_US
dc.subjectChickpeaen_US
dc.subjectflowering timeen_US
dc.subjectInDelen_US
dc.subjectmaturity timeen_US
dc.subjectQTLen_US
dc.titleGenome-wide insertion-deletion (InDel) marker discovery and genotyping for genomics- assisted breeding applications in chickpeaen_US
dc.typeArticleen_US
dc.identifier.officialurlhttp://dnaresearch.oxfordjournals.org/content/22/5/377en_US
dc.identifier.doi10.1093/dnares/dsv020en_US
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