HOU Rong
State Key Laboratory of Genetic Engineering, Institute of Plant Biology, School of Life Sciences, Fudan University, ChinaGONG Nuo-xi
State Key Laboratory of Genetic Engineering, Institute of Plant Biology, School of Life Sciences, Fudan University, ChinaLIU Fa-tao
State Key Laboratory of Genetic Engineering, Institute of Plant Biology, School of Life Sciences, Fudan University, ChinaLIN Juan
State Key Laboratory of Genetic Engineering, Institute of Plant Biology, School of Life Sciences, Fudan University, ChinaUsing the total RNA extracted from Jatropha curcas L. leaves as the template, the degenerate primers were designed according to the reported sequence of squalene synthases gene in other plants, the full-length cDNA of squalene synthase gene in Jatropha curcas L. was cloned using RACE method, which was named JcSQS with 1609 bp in length including a 1242 bp-ORF, and JcSQS was predicted to encode the protein with 413 amino acids. The cloned JcSQS gene contained the typical conserved sequences and domains of SQS genes. The JcSQS protein had high homology with the amino acid sequences encoded by SQS gene in Ricinus communis, Diospyros kaki and Bruguiera gymnorhiza, so on. It laid the foundation for studying the biosynthesis and regulation of terpenoids and steroids in J. curcas.
侯嵘,龚诺希,刘法涛,林娟.麻疯树鲨烯合酶基因SQS的克隆及生物信息学分析[J].热带亚热带植物学报,2011,19(5):391~399
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