Luo Zhi-Yong, Lu Qiu-Heng, Liu Shui-Ping, Chen Xiang-Hui, Luo Jian-Qing, Tan Li-Jun, Hu Wei-Xin
Molecular Biology Research Centre, Xiangya Medical College, Central South University, Changsha 410078, China.
Sheng Wu Hua Xue Yu Sheng Wu Wu Li Xue Bao (Shanghai). 2003 Jun;35(6):554-60.
The root of Panax ginseng plant undergoes a specific developmental process to become a biosynthesis and accumulation organ for ginsenosides. To identify and analyze genes involved in the biosynthesis of ginsenoside, suppression subtractive hybridization (SSH) between mRNAs of 4- and 1-year-old root tissues was performed, and a subtracted cDNA library specific to 4-year-old roots was constructed. Forty cDNA clones selected randomly from the subtracted cDNA library were sequenced. Sequence information of all clones was evaluated by Nucleotide Blast analysis in GenBank/DDBJ/EMBL. The results showed that six subtracted cDNA clones represented the novel genes (ESTs), because no sequence homology with any known sequences was found in the database. Expression in 4-year-old P. ginseng root tissues was verified by reverse Northern dot hybridization for the six clones. These six novel genes were named GBR1, GBR2, GBR3, GBR4, GBR5, and GBR6, and their Accession numbers of GenBank are AF485334, AF485335, AF485336, AF485337, AF485332, and AF485333, respectively. Finally, Northern blot analysis and semi-quantitative reverse transcription polymerase chain reaction (RT-PCR) confirmed that these six novel genes were differentially expressed in the defined development stage of P. ginseng plant roots. It is possible that their overexpression may play an important role in the ginsenoside biosynthesis. In addition, most of transcripts of all genes could also be detected in other P. ginseng plant tissues such as stem, leaf and seed. Our results provided a basis for obtaining the full-length cDNA sequences of such six novel genes, and for identifying their function involved in the biosynthesis of ginsenoside.
人参植株的根会经历一个特定的发育过程,从而成为人参皂苷的生物合成与积累器官。为了鉴定和分析参与人参皂苷生物合成的基因,我们对4年生和1年生根组织的mRNA进行了抑制性消减杂交(SSH),并构建了一个4年生根特异的消减cDNA文库。从该消减cDNA文库中随机挑选了40个cDNA克隆进行测序。所有克隆的序列信息通过GenBank/DDBJ/EMBL中的核苷酸比对分析进行评估。结果表明,有6个消减cDNA克隆代表了新基因(ESTs),因为在数据库中未发现与任何已知序列的同源性。通过反向Northern斑点杂交对这6个克隆在4年生人参根组织中的表达进行了验证。这6个新基因分别命名为GBR1、GBR2、GBR3、GBR4、GBR5和GBR6,它们在GenBank中的登录号分别为AF485334、AF485335、AF485336、AF485337、AF485332和AF485333。最后,Northern印迹分析和半定量逆转录聚合酶链反应(RT-PCR)证实,这6个新基因在人参植株根的特定发育阶段存在差异表达。它们的过表达可能在人参皂苷生物合成中发挥重要作用。此外,在人参植株的其他组织如茎、叶和种子中也能检测到所有基因的大部分转录本。我们的结果为获得这6个新基因的全长cDNA序列以及鉴定它们在人参皂苷生物合成中的功能提供了基础。