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dc.contributorUpadhyaya, Hari D.en_US
dc.contributorSrivastava, Rishien_US
dc.contributorBajaj, Deepaken_US
dc.contributorGowda, C. L. L.en_US
dc.contributorSharma, Shivalien_US
dc.contributorSingh, Subeen_US
dc.contributorTyagi, Akhilesh K.en_US
dc.contributorParida, Swarup K.en_US
dc.creatorDas, Shouviken_US
dc.date.accessioned2017-05-15T18:53:01Z
dc.date.available2017-05-15T18:53:01Z
dc.identifierhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4596403/en_US
dc.identifierhttps://mel.cgiar.org/reporting/download/hash/8DaTBcmeen_US
dc.identifier.citationShouvik Das, Hari D. Upadhyaya, Rishi Srivastava, Deepak Bajaj, C. L. L. Gowda, Shivali Sharma, Sube Singh, Akhilesh K. Tyagi, Swarup K. Parida. (15/9/2015). Genome-wide insertion–deletion (InDel) marker discovery and genotyping for genomics-assisted breeding applications in chickpea. DNA Research, 22 (5), pp. 377-386.en_US
dc.identifier.urihttps://hdl.handle.net/20.500.11766/7003
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.formatPDFen_US
dc.languageenen_US
dc.publisherOxford University Press (OUP)en_US
dc.rightsCC-BY-NC-4.0en_US
dc.sourceDNA Research;22,(2015) Pagination 377-386en_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.typeJournal Articleen_US
dcterms.available2015-09-15en_US
dcterms.extent377-386en_US
cg.subject.agrovocplant genetic resourcesen_US
cg.subject.agrovocflowering timeen_US
cg.subject.agrovocChickpeaen_US
cg.contributor.centerInternational Crops Research Institute for the Semi-Arid Tropics - ICRISATen_US
cg.contributor.centerNational Institute of Plant Genome Research - NIPGRen_US
cg.contributor.crpCGIAR Research Program on Grain Legumes - GLen_US
cg.contributor.funderNot Applicableen_US
cg.contributor.project-lead-instituteInternational Center for Agricultural Research in the Dry Areas - ICARDAen_US
cg.coverage.regionSouthern Asiaen_US
cg.coverage.countryINen_US
cg.contactswarup@nipgr.ac.inen_US
cg.identifier.doihttps://dx.doi.org/10.1093/dnares/dsv020en_US
cg.isijournalISI Journalen_US
dc.identifier.statusOpen accessen_US
mel.impact-factor5.267en_US
cg.issn1340-2838en_US
cg.journalDNA Researchen_US
cg.issue5en_US
cg.volume22en_US


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