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刺山柑转录组分析为伞形科萜类生物合成及多样性研究提供见解。

Transcriptome analysis of Thapsia laciniata Rouy provides insights into terpenoid biosynthesis and diversity in Apiaceae.

作者信息

Drew Damian Paul, Dueholm Bjørn, Weitzel Corinna, Zhang Ye, Sensen Christoph W, Simonsen Henrik Toft

机构信息

Department of Plant and Environmental Sciences, Faculty of Sciences, University of Copenhagen, Frederiksberg DK-1871, Denmark.

出版信息

Int J Mol Sci. 2013 Apr 25;14(5):9080-98. doi: 10.3390/ijms14059080.

DOI:10.3390/ijms14059080
PMID:23698765
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3676774/
Abstract

Thapsia laciniata Rouy (Apiaceae) produces irregular and regular sesquiterpenoids with thapsane and guaiene carbon skeletons, as found in other Apiaceae species. A transcriptomic analysis utilizing Illumina next-generation sequencing enabled the identification of novel genes involved in the biosynthesis of terpenoids in Thapsia. From 66.78 million HQ paired-end reads obtained from T. laciniata roots, 64.58 million were assembled into 76,565 contigs (N50: 1261 bp). Seventeen contigs were annotated as terpene synthases and five of these were predicted to be sesquiterpene synthases. Of the 67 contigs annotated as cytochromes P450, 18 of these are part of the CYP71 clade that primarily performs hydroxylations of specialized metabolites. Three contigs annotated as aldehyde dehydrogenases grouped phylogenetically with the characterized ALDH1 from Artemisia annua and three contigs annotated as alcohol dehydrogenases grouped with the recently described ADH1 from A. annua. ALDH1 and ADH1 were characterized as part of the artemisinin biosynthesis. We have produced a comprehensive EST dataset for T. laciniata roots, which contains a large sample of the T. laciniata transcriptome. These transcriptome data provide the foundation for future research into the molecular basis for terpenoid biosynthesis in Thapsia and on the evolution of terpenoids in Apiaceae.

摘要

刺续断(伞形科)产生具有紫铆烷和愈创木烷碳骨架的不规则和规则倍半萜,这在其他伞形科植物中也有发现。利用Illumina下一代测序技术进行的转录组分析,能够鉴定出参与刺续断萜类生物合成的新基因。从刺续断根中获得的6678万个高质量双端读数中,有6458万个被组装成76565个重叠群(N50:1261 bp)。17个重叠群被注释为萜类合酶,其中5个被预测为倍半萜合酶。在67个被注释为细胞色素P450的重叠群中,有18个是CYP71进化枝的一部分,该进化枝主要负责特殊代谢产物的羟基化。3个被注释为醛脱氢酶的重叠群在系统发育上与青蒿中已鉴定的ALDH1聚在一起,3个被注释为醇脱氢酶的重叠群与最近描述的青蒿ADH1聚在一起。ALDH1和ADH1被鉴定为青蒿素生物合成的一部分。我们已经为刺续断根生成了一个全面的EST数据集,其中包含刺续断转录组的大量样本。这些转录组数据为未来研究刺续断萜类生物合成的分子基础以及伞形科萜类的进化提供了基础。

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