Please use this identifier to cite or link to this item: http://223.31.159.10:8080/jspui/handle/123456789/690
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dc.contributor.authorDaware, Anurag-
dc.contributor.authorDas, Sweta-
dc.contributor.authorSrivastava, Rishi-
dc.contributor.authorBadoni, Saurabh-
dc.contributor.authorSingh, Ashok K.-
dc.contributor.authorAgarwal, Pinky-
dc.contributor.authorParida, Swarup K.-
dc.contributor.authorTyagi, Akhilesh K.-
dc.date.accessioned2016-11-04T09:02:20Z-
dc.date.available2016-11-04T09:02:20Z-
dc.date.issued2016-
dc.identifier.citationFront. Plant Sc., 7: 1535en_US
dc.identifier.issn1664-462X-
dc.identifier.urihttp://59.163.192.83:8080/jspui/handle/123456789/690-
dc.descriptionAccepted date: 29 September 2016en_US
dc.description.abstractDevelopment and use of genome-wide informative simple sequence repeat (SSR) markers and novel integrated genomic strategies are vital to drive genomics-assisted breeding applications and for efficient dissection of quantitative trait loci (QTLs) underlying complex traits in rice. The present study developed 6244 genome-wide informative SSR markers exhibiting in silico fragment length polymorphism based on repeat-unit variations among genomic sequences of 11 indica, japonica, aus, and wild rice accessions. These markers were mapped on diverse coding and non-coding sequence components of known cloned/candidate genes annotated from 12 chromosomes and revealed a much higher amplification (97%) and polymorphic potential (88%) along with wider genetic/functional diversity level (16–74% with a mean 53%) especially among accessions belonging to indica cultivar group, suggesting their utility in large-scale genomics-assisted breeding applications in rice. A high-density 3791 SSR markers-anchored genetic linkage map (IR 64 × Sonasal) spanning 2060 cM total map-length with an average inter-marker distance of 0.54 cM was generated. This reference genetic map identified six major genomic regions harboring robust QTLs (31% combined phenotypic variation explained with a 5.7–8.7 LOD) governing grain weight on six rice chromosomes. One strong grain weight major QTL region (OsqGW5.1) was narrowed-down by integrating traditional QTL mapping with high-resolution QTL region-specific integrated SSR and single nucleotide polymorphism markers-based QTL-seq analysis and differential expression profiling. This led us to delineate two natural allelic variants in two known cis-regulatory elements (RAV1AAT and CARGCW8GAT) of glycosyl hydrolase and serine carboxypeptidase genes exhibiting pronounced seed-specific differential regulation in low (Sonasal) and high (IR 64) grain weight mapping parental accessions. Our genome-wide SSR marker resource (polymorphic within/between diverse cultivar groups) and integrated genomic strategy can efficiently scan functionally relevant potential molecular tags (markers, candidate genes and alleles) regulating complex agronomic traits (grain weight) and expedite marker-assisted genetic enhancement in rice.en_US
dc.description.sponsorshipThe authors gratefully acknowledge the financial support for this study provided by a research grant from the Department of Biotechnology (DBT), Government of India (102/IFD/SAN/2161/2013-14)en_US
dc.language.isoen_USen_US
dc.publisherFrontiers Media S.A.en_US
dc.subjectgrain weighten_US
dc.subjectQTLen_US
dc.subjectQTL-seqen_US
dc.subjectriceen_US
dc.subjectSNPen_US
dc.subjectSSRen_US
dc.titleAn efficient strategy combining SSR markers- and advanced QTL-seq-driven QTL mapping unravels candidate genes regulating grain weight in riceen_US
dc.typeArticleen_US
dc.identifier.officialurlhttp://journal.frontiersin.org/article/10.3389/fpls.2016.01535/fullen_US
dc.identifier.doi10.3389/fpls.2016.01535en_US
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