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通过全长 cDNA 测序鉴定 中的萜类生物合成基因。

Identifying Terpenoid Biosynthesis Genes in via Full-Length cDNA Sequencing.

机构信息

Microorganism Resources Division, National Institute of Biological Resources, Incheon 22689, Korea.

Agriculture and Life Sciences Research Institute, Kangwon National University, Chuncheon 24341, Korea.

出版信息

Molecules. 2022 Jul 19;27(14):4591. doi: 10.3390/molecules27144591.

Abstract

The annual herb L. produces anti-inflammatory and biologically active substances such as triterpenoids, tannins, and polyphenols, and it is used in traditional Chinese medicine. Of these bioactive compounds, terpenoids, also called isoprenoids, are major secondary metabolites in . Full-length cDNA sequencing was carried out to characterize the transcripts of terpenoid biosynthesis reference genes and determine the copy numbers of their isoforms using PacBio SMRT sequencing technology. The Illumina short-read sequencing platform was also employed to identify differentially expressed genes (DEGs) in the secondary metabolite pathways from leaves, roots, and stems. PacBio generated 62 million polymerase reads, resulting in 81,433 high-quality reads. From these high-quality reads, we reconstructed a genome of 20,722 genes, in which 20,246 genes (97.8%) did not have paralogs. About 33% of the identified genes had two or more isoforms. DEG analysis revealed that the expression level differed among gene paralogs in the leaf, stem, and root. Whole sets of paralogs and isoforms were identified in the mevalonic acid (MVA), methylerythritol phosphate (MEP), and terpenoid biosynthesis pathways in the L. The nucleotide information will be useful for identifying orthologous genes in other terpenoid-producing medicinal plants.

摘要

一年生草本植物 L. 产生抗炎和生物活性物质,如三萜类、单宁和多酚,它被用于中药。在这些生物活性化合物中,萜类化合物,也称为异戊二烯类,是 L. 的主要次生代谢物。进行全长 cDNA 测序,以表征萜类生物合成参考基因的转录本,并使用 PacBio SMRT 测序技术确定其同工型的拷贝数。还使用 Illumina 短读测序平台鉴定来自叶片、根和茎的次生代谢途径中的差异表达基因 (DEG)。PacBio 产生了 6200 万个聚合酶读取,产生了 81433 个高质量读取。从这些高质量读取中,我们重建了一个包含 20722 个基因的基因组,其中 20246 个基因(97.8%)没有旁系同源基因。大约 33%的鉴定基因有两个或更多的同工型。DEG 分析表明,在叶、茎和根中,基因旁系同源物的表达水平不同。在 L. 的甲羟戊酸(MVA)、甲基赤藓醇磷酸(MEP)和萜类生物合成途径中,鉴定出了整套的旁系同源基因和同工型。核苷酸信息将有助于鉴定其他萜类生产药用植物中的同源基因。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/873f/9316252/be144731d59e/molecules-27-04591-g001.jpg

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