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dc.contributor.authorLata, Charu-
dc.contributor.authorBhutty, Sarita-
dc.contributor.authorBahadur, Ranjit Prasad-
dc.contributor.authorMajee, Manoj-
dc.contributor.authorPrasad, Manoj-
dc.date.accessioned2014-04-30T05:23:44Z-
dc.date.available2014-04-30T05:23:44Z-
dc.date.issued2011-
dc.identifier.citationJ. Exp. Bot., 62(10): 3387-3401en_US
dc.identifier.urihttp://hdl.handle.net/123456789/203-
dc.description.abstractThe DREB genes code for important plant transcription factors involved in the abiotic stress response and signal transduction. Characterization of DREB genes and development of functional markers for effective alleles is important for marker-assisted selection in foxtail millet. Here the characterization of a cDNA (SiDREB2) encoding a putative dehydration-responsive element-binding protein 2 from foxtail millet and the development of an allele-specific marker (ASM) for dehydration tolerance is reported. A cDNA clone (GenBank accession no. GT090998) coding for a putative DREB2 protein was isolated as a differentially expressed gene from a 6 h dehydration stress SSH library. A 5' RACE (rapid amplification of cDNA ends) was carried out to obtain the full-length cDNA, and sequence analysis showed that SiDREB2 encoded a polypeptide of 234 amino acids with a predicted mol. wt of 25.72 kDa and a theoretical pI of 5.14. A theoretical model of the tertiary structure shows that it has a highly conserved GCC-box-binding N-terminal domain, and an acidic C-terminus that acts as an activation domain for transcription. Based on its similarity to AP2 domains, SiDREB2 was classified into the A-2 subgroup of the DREB subfamily. Quantitative real-time PCR analysis showed significant up-regulation of SiDREB2 by dehydration (polyethylene glycol) and salinity (NaCl), while its expression was less affected by other stresses. A synonymous single nucleotide polymorphism (SNP) associated with dehydration tolerance was detected at the 558th base pair (an A/G transition) in the SiDREB2 gene in a core set of 45 foxtail millet accessions used. Based on the identified SNP, three primers were designed to develop an ASM for dehydration tolerance. The ASM produced a 261 bp fragment in all the tolerant accessions and produced no amplification in the sensitive accessions. The use of this ASM might be faster, cheaper, and more reproducible than other SNP genotyping methods, and thus will enable marker-aided breeding of foxtail millet for dehydration tolerance.en_US
dc.description.sponsorshipThis study was supported by the Department of Biotechnology (grant no. BT/PR9851/AGR/02/521/2007), the Government of India, New Delhi, and a core grant from the National Institute of Plant Genome Researchen_US
dc.language.isoenen_US
dc.publisherOxford University Pressen_US
dc.subjectAllele-specific markeren_US
dc.subjectdehydration-responsive element-binding protein 2en_US
dc.subjectdehydration stressen_US
dc.subjectgene expressionen_US
dc.subjectSetaria italicaen_US
dc.subjectsingle nucleotide polymorphismen_US
dc.titleAssociation of SNP in a novel DREB2-like gene SiDREB2 with stress tolerance in foxtail millet [Setaria italica (L.)]en_US
dc.typeArticleen_US
dc.date.AcceptedDate13 January 2011en_US
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