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比较转录组分析鉴定两种伊朗特有药用植物香薄荷中参与香芹酚生物合成途径的假定基因。

Comparative transcriptome analysis to identify putative genes involved in carvacrol biosynthesis pathway in two species of Satureja, endemic medicinal herbs of Iran.

机构信息

Faculty of Agriculture, Department of Plant Production and Genetic Engineering, Lorestan University, Khorramabad, Iran.

Faculty of Agriculture, Department of Horticultural Science, Lorestan University, Khorramabad, Iran.

出版信息

PLoS One. 2023 Jul 7;18(7):e0281351. doi: 10.1371/journal.pone.0281351. eCollection 2023.

Abstract

Satureja is rich in phenolic monoterpenoids, mainly carvacrol, that is of interest due to diverse biological activities including antifungal and antibacterial. However, limited information is available regarding the molecular mechanisms underlying carvacrol biosynthesis and its regulation for this wonderful medicinal herb. To identify the putative genes involved in carvacrol and other monoterpene biosynthesis pathway, we generated a reference transcriptome in two endemic Satureja species of Iran, containing different yields (Satureja khuzistanica and Satureja rechingeri). Cross-species differential expression analysis was conducted between two species of Satureja. 210 and 186 transcripts related to terpenoid backbone biosynthesis were identified for S. khuzistanica and S. rechingeri, respectively. 29 differentially expressed genes (DEGs) involved in terpenoid biosynthesis were identified, and these DEGs were significantly enriched in monoterpenoid biosynthesis, diterpenoid biosynthesis, sesquiterpenoid and triterpenoid biosynthesis, carotenoid biosynthesis and ubiquinone and other terpenoid-quinone biosynthesis pathways. Expression patterns of S. khuzistanica and S. rechingeri transcripts involved in the terpenoid biosynthetic pathway were evaluated. In addition, we identified 19 differentially expressed transcription factors (such as MYC4, bHLH, and ARF18) that may control terpenoid biosynthesis. We confirmed the altered expression levels of DEGs that encode carvacrol biosynthetic enzymes using quantitative real-time PCR (qRT-PCR). This study is the first report on de novo assembly and transcriptome data analysis in Satureja which could be useful for an understanding of the main constituents of Satureja essential oil and future research in this genus.

摘要

香薷富含酚类单萜,主要为香芹酚,由于具有多种生物活性,包括抗真菌和抗菌活性,因此引起了人们的关注。然而,关于香芹酚生物合成及其调控的分子机制,对于这种奇妙的药用植物,相关信息有限。为了鉴定参与香芹酚和其他单萜生物合成途径的假定基因,我们在伊朗两种特有香薷物种(Satureja khuzistanica 和 Satureja rechingeri)中生成了一个参考转录组,它们的产量不同。在两种香薷物种之间进行了跨物种差异表达分析。分别为 S. khuzistanica 和 S. rechingeri 鉴定了与萜类骨架生物合成相关的 210 和 186 个转录本。鉴定了 29 个参与萜类生物合成的差异表达基因(DEG),这些 DEG 显著富集在单萜生物合成、二萜生物合成、倍半萜和三萜生物合成、类胡萝卜素生物合成以及泛醌和其他萜类-醌生物合成途径中。评估了参与萜类生物合成途径的 S. khuzistanica 和 S. rechingeri 转录本的表达模式。此外,我们鉴定了 19 个差异表达的转录因子(如 MYC4、bHLH 和 ARF18),它们可能控制萜类生物合成。我们使用定量实时 PCR(qRT-PCR)验证了编码香芹酚生物合成酶的 DEG 的改变表达水平。这项研究是首次在香薷中进行从头组装和转录组数据分析的报告,这对于理解香薷精油的主要成分以及该属的未来研究可能有用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/704c/10328369/7717cb07f48d/pone.0281351.g001.jpg

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