Cloning and Expression Analysis of 2oxoglutaratedependent Dioxygenase from Salvia miltiorrhiza Bunge
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    Abstract:

    By analyzing Transcriptome (SRA020132) sequences of Salvia miltiorrhiza from Shangluo and using the techniques of PCR,a new 2oxoglutaratedependent dioxygenase gene was cloned from Salvia miltiorrhiza for the first time and named as Sm2ODD1 (GenBank accession number JN935923).Sm2ODD1 DNA consisted of 1 365 bp including 3 exons and 2 introns.The fulllength cDNA of Sm2ODD1 was 1 189 bp,containing a single 951 bp opening reading frame and encoding a 316 aminoacid residues.Bioinformatics analysis showed that Sm2ODD1 contained a 2oxoglutaratedependent dioxygenase superfamily containing “distorted jelly roll” domain and “HTD”,“HX” and “RYS” motifs to bind 2oxoglutarate and Fe2+.Quantitative RTPCR analysis revealed that the gene expressed in different organs.The expression in roots was observably higher than in flowers,stems and leaves.The gene could be induced by methyl jasmonate,GA3 and ABA.The results indicated that the Sm2ODD1 might be involved in the biosynthesis of terpene in Salvia miltiorrhiza.

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LIU Wenchao, WANG Donghao, WANG Zhezhi, LI Cuiqin. Cloning and Expression Analysis of 2oxoglutaratedependent Dioxygenase from Salvia miltiorrhiza Bunge[J]. Acta Botanica Boreali-Occidentalia Sinica,2012,32(7):1289-1294

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  • Online: July 26,2012
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