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采用深度测序和转录组分析鉴定细辛中与马兜铃酸生物合成相关的基因。

Deep sequencing and transcriptome analysis to identify genes related to biosynthesis of aristolochic acid in Asarum heterotropoides.

机构信息

Traditional Chinese Medicine College, Jilin Agricultural University, Changchun City, Jilin Province, 130118, China.

出版信息

Sci Rep. 2018 Dec 14;8(1):17850. doi: 10.1038/s41598-018-36316-0.

Abstract

Asarum spp. are important medicinal plants that have the potential for use in treating various types of fevers. Aristolochic acid is one of the main toxic compounds present in these plants. To improve our understanding of the biosynthetic pathway of aristolochic acid, we sequenced the transcriptome of the root and leaf tissues of Asarum heterotropoides and performed de novo sequence assembly. The data were stitched together to produce 468,357 transcripts with an N50 of 611 bp. The data were annotated with various databases (RefSeq non-redundant proteins [Nr], Swiss-Prot, Kyoto Encyclopaedia of Genes and Genomes [KEGG], Clusters of Orthologous Groups/EuKaryotic Orthologous Groups [COG/KOG], and Gene Ontology [GO]) and were annotated. There were 205,165 transcripts (43.81%) of differentially expressed genes in the roots and leaves, which were shown to be involved in biosynthesis, transport, and catabolism, and 100 genes in defence mechanisms. Three candidate transcripts (TyrDC1, TyrDC2, and TyrDC3) were discovered in these differential genes. TyrDC may be a key enzyme in the biosynthesis pathway of aristolochic acid identified using quantitative reverse transcription-polymerase chain reaction (qRT-PCR) and high-performance liquid chromatography (HPLC). The transcriptome data and analysis presented here lay the foundation for further research into these important medicinal plants.

摘要

细辛属植物是重要的药用植物,具有治疗各种发热的潜力。马兜铃酸是这些植物中主要的有毒化合物之一。为了提高我们对马兜铃酸生物合成途径的认识,我们对北细辛的根和叶组织进行了转录组测序,并进行了从头序列组装。将数据拼接在一起,产生了 468357 个转录本,N50 为 611bp。将数据注释到各种数据库(RefSeq 非冗余蛋白[Nr]、Swiss-Prot、京都基因与基因组百科全书[KEGG]、直系同源群/真核直系同源群[COG/KOG]和基因本体论[GO])中,并进行了注释。在根和叶中有 205165 个差异表达基因的转录本(43.81%),这些转录本被证明参与了生物合成、运输和分解代谢,以及 100 个防御机制基因。在这些差异基因中发现了 3 个候选转录本(TyrDC1、TyrDC2 和 TyrDC3)。TyrDC 可能是使用定量逆转录聚合酶链反应(qRT-PCR)和高效液相色谱(HPLC)鉴定的马兜铃酸生物合成途径中的关键酶。这里提供的转录组数据和分析为进一步研究这些重要的药用植物奠定了基础。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a6e2/6294785/e0d6efe631eb/41598_2018_36316_Fig1_HTML.jpg

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