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Transcriptome analysis of Bupleurum chinense focusing on genes involved in the biosynthesis of saikosaponins

机译:柴胡的转录组分析,侧重于皂角苷生物合成相关基因

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Background Bupleurum chinense DC. is a widely used traditional Chinese medicinal plant. Saikosaponins are the major bioactive constituents of B. chinense, but relatively little is known about saikosaponin biosynthesis. The 454 pyrosequencing technology provides a promising opportunity for finding novel genes that participate in plant metabolism. Consequently, this technology may help to identify the candidate genes involved in the saikosaponin biosynthetic pathway. Results One-quarter of the 454 pyrosequencing runs produced a total of 195, 088 high-quality reads, with an average read length of 356 bases (NCBI SRA accession SRA039388). A de novo assembly generated 24, 037 unique sequences (22, 748 contigs and 1, 289 singletons), 12, 649 (52.6%) of which were annotated against three public protein databases using a basic local alignment search tool (E-value ≤1e-10). All unique sequences were compared with NCBI expressed sequence tags (ESTs) (237) and encoding sequences (44) from the Bupleurum genus, and with a Sanger-sequenced EST dataset (3, 111). The 23, 173 (96.4%) unique sequences obtained in the present study represent novel Bupleurum genes. The ESTs of genes related to saikosaponin biosynthesis were found to encode known enzymes that catalyze the formation of the saikosaponin backbone; 246 cytochrome P450 (P450s) and 102 glycosyltransferases (GTs) unique sequences were also found in the 454 dataset. Full length cDNAs of 7 P450s and 7 uridine diphosphate GTs (UGTs) were verified by reverse transcriptase polymerase chain reaction or by cloning using 5' and/or 3' rapid amplification of cDNA ends. Two P450s and three UGTs were identified as the most likely candidates involved in saikosaponin biosynthesis. This finding was based on the coordinate up-regulation of their expression with β-AS in methyl jasmonate-treated adventitious roots and on their similar expression patterns with β-AS in various B. chinense tissues. A collection of high-quality ESTs for B. chinense obtained by 454 pyrosequencing is provided here for the first time. These data should aid further research on the functional genomics of B. chinense and other Bupleurum species. The candidate genes for enzymes involved in saikosaponin biosynthesis, especially the P450s and UGTs, that were revealed provide a substantial foundation for follow-up research on the metabolism and regulation of the saikosaponins.
机译:背景柴胡DC。是一种广泛使用的中药材。皂苷皂苷是中国双歧杆菌的主要生物活性成分,但对皂苷皂苷的生物合成知之甚少。 454焦磷酸测序技术为寻找参与植物代谢的新基因提供了一个有前途的机会。因此,该技术可能有助于鉴定参与皂苷皂苷生物合成途径的候选基因。结果454次焦磷酸测序运行中,有四分之一产生了195个,088个高质量的读段,平均读长为356个碱基(NCBI SRA登录号SRA039388)。从头装配产生了24、037个独特序列(22、748个重叠群和1,289个单例),其中12个,649个(52.6%)使用基本的局部比对搜索工具针对三个公共蛋白质数据库进行了注释(E值≤ 1e-10)。将所有唯一序列与柴胡属的NCBI表达序列标签(EST)(237)和编码序列(44)以及Sanger测序EST数据集(3,111)进行比较。在本研究中获得的23、173(96.4%)个唯一序列代表了新柴胡基因。发现与皂苷皂苷生物合成有关的基因的EST编码了已知的催化皂苷皂苷骨架形成的酶。在454数据集中还发现了246个细胞色素P450(P450s)和102个糖基转移酶(GTs)独特序列。通过逆转录聚合酶链反应或使用5'和/或3'快速扩增cDNA末端进行克隆,验证了7个P450和7个尿苷二磷酸GT(UGT)的全长cDNA。确定了两个P450和三个UGT作为赛果皂苷生物合成中最可能的候选物。这一发现是基于茉莉酸甲酯处理的不定根中β-AS的协同表达上调,以及在各种B. chinense组织中β-AS的相似表达模式。此处首次提供了通过454焦磷酸测序获得的优质B. chinest EST的集合。这些数据应有助于进一步研究中国双歧杆菌和其他柴胡种的功能基因组学。揭示了参与皂苷皂苷生物合成的酶的候选基因,特别是P450和UGT,为后续研究皂苷皂苷的代谢和调控提供了坚实的基础。

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