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沉香属萜烯合酶基因家族的全基因组鉴定和表达分析。

Genome-wide identification and expression analysis of terpene synthase gene family in Aquilaria sinensis.

机构信息

Key Laboratory of Biology and Genetic Resources of Tropical Crops, Ministry of Agriculture, Institute of Tropical Bioscience and Biotechnology, Chinese Academy of Tropical Agricultural Sciences, Haikou, 571101, China; College of Life Science and Technology, Heilongjiang Bayi Agricultural University, Daqing, 163000, China.

Key Laboratory of Biology and Genetic Resources of Tropical Crops, Ministry of Agriculture, Institute of Tropical Bioscience and Biotechnology, Chinese Academy of Tropical Agricultural Sciences, Haikou, 571101, China.

出版信息

Plant Physiol Biochem. 2021 Jul;164:185-194. doi: 10.1016/j.plaphy.2021.04.028. Epub 2021 May 12.

Abstract

Agarwood is the resinous portion of Aquilaria trees, and has been widely used as medicine and incense. Sesquiterpenes are the main chemical characteristic constituents of agarwood. Terpene synthase (TPS) is a critical enzyme responsible for biosynthesis of sesquiterpene compounds. However, limited information is available on genome-wide identification and characterization of the TPS family in Aquilaria trees. In this study, TPS gene family was identified and characterized in Aquilaria sinensis by bioinformatics methods. The expression of those genes was analyzed by RNA-seq and quantitative real-time PCR. Transcription factors regulating TPS gene expression were identified by yeast one-hybrid and dual-luciferase assay. In total, 26 AsTPS genes (AsTPS1-AsTPS26) were identified, which were classified into five subgroups. Many putative cis-elements putatively involved in stresses and phytohormones (especially jasmonic acid) were identified in the promoter regions of AsTPSs, suggesting that AsTPSs genes may be regulated by stresses and jasmonic acid. Expression analysis revealed seven TPS genes encoding sesquiterpene synthetases were induced by wounding and methyl jasmonic acid (MeJA), which may be related to sesquiterpene biosynthesis. By yeast one-hybrid screening, a ERF transcription factor AsERF1 was identified to interact with the AsTPS1 promoter. Subcellular localization analysis indicated AsERF1 was a nucleus-localized protein. Transient transfection of AsERF1 in leaves of Nicotiana benthamiana significantly enhanced the promoter activation of AsTPS1, suggesting AsERF1 may participate in sesquiterpene biosynthesis by regulating AsTPS1 expression. These data generated in this study provide a foundation for future studies on functional roles and regulation mechanisms of AsTPS in sesquiterpene biosynthesis and agarwood formation.

摘要

沉香是瑞香科树木的树脂部分,被广泛用作药物和香料。倍半萜烯是沉香的主要化学特征成分。萜烯合酶(TPS)是负责合成倍半萜烯化合物的关键酶。然而,关于沉香树木基因组范围内TPS 家族的鉴定和特征研究还很有限。本研究通过生物信息学方法鉴定和分析了沉香中的 TPS 基因家族。通过 RNA-seq 和定量实时 PCR 分析了这些基因的表达。通过酵母单杂交和双荧光素酶测定鉴定了调节 TPS 基因表达的转录因子。共鉴定了 26 个 AsTPS 基因(AsTPS1-AsTPS26),分为五个亚组。在 AsTPSs 启动子区域鉴定到许多假定参与应激和植物激素(特别是茉莉酸)的顺式作用元件,表明 AsTPSs 基因可能受到应激和茉莉酸的调节。表达分析显示,编码倍半萜合酶的 7 个 TPS 基因被创伤和茉莉酸甲酯(MeJA)诱导,这可能与倍半萜合成有关。通过酵母单杂交筛选,鉴定到一个 ERF 转录因子 AsERF1 与 AsTPS1 启动子相互作用。亚细胞定位分析表明 AsERF1 是一种核定位蛋白。在 Nicotiana benthamiana 的叶片中转瞬表达 AsERF1 显著增强了 AsTPS1 启动子的激活,表明 AsERF1 可能通过调节 AsTPS1 的表达参与倍半萜合成。本研究提供的这些数据为进一步研究 AsTPS 在倍半萜合成和沉香形成中的功能作用和调控机制奠定了基础。

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