曹芳, 夏菁, 陈俞裴, 张曼, 向礼恩, 曾俊岚, 陈敏, 兰小中, 廖志华. 黄花蒿羟甲基丁烯基-4-磷酸还原酶基因克隆与功能研究J. 药学学报, 2016,51(11): 1791-1798. doi: 10.16438/j.0513-4870.2016-0246
引用本文: 曹芳, 夏菁, 陈俞裴, 张曼, 向礼恩, 曾俊岚, 陈敏, 兰小中, 廖志华. 黄花蒿羟甲基丁烯基-4-磷酸还原酶基因克隆与功能研究J. 药学学报, 2016,51(11): 1791-1798. doi: 10.16438/j.0513-4870.2016-0246
CAO Fang, XIA Jing, CHEN Yu-pei, ZHANG Man, XIANG Li-en, ZENG Jun-lan, CHEN Min, LAN Xiao-zhong, LIAO Zhi-hua. Molecular cloning and functional characterization of the gene encoding hydroxy-2-methyl-2-(E)-butenyl 4-diphosphate reductase gene from Artemisia annua L.J. Acta Pharmaceutica Sinica, 2016,51(11): 1791-1798. doi: 10.16438/j.0513-4870.2016-0246
Citation: CAO Fang, XIA Jing, CHEN Yu-pei, ZHANG Man, XIANG Li-en, ZENG Jun-lan, CHEN Min, LAN Xiao-zhong, LIAO Zhi-hua. Molecular cloning and functional characterization of the gene encoding hydroxy-2-methyl-2-(E)-butenyl 4-diphosphate reductase gene from Artemisia annua L.J. Acta Pharmaceutica Sinica, 2016,51(11): 1791-1798. doi: 10.16438/j.0513-4870.2016-0246

黄花蒿羟甲基丁烯基-4-磷酸还原酶基因克隆与功能研究

Molecular cloning and functional characterization of the gene encoding hydroxy-2-methyl-2-(E)-butenyl 4-diphosphate reductase gene from Artemisia annua L.

  • 摘要: 青蒿素是治疗疟疾的首选药物,定位于质体的MEP途径可为青蒿素在内的萜类物质的合成提供基本前体。羟甲基丁烯基-4-磷酸还原酶hydroxy-2-methyl-2-(E)-butenyl 4-diphosphate reductase,HDR是MEP途径最后一个酶,催化HMBPP生成IPP和IPP的同分异构体DMAPP。本文克隆了黄花蒿HDR基因(AaHDR2)并进行了相关功能研究。通过对AaHDR2基因(GenBank:KX058541)和已报道的AaHDR1基因(GenBank:ADC84348.1)表达分析结果表明:AaHDR1AaHDR2在黄花蒿腺体中表达量均远高于在根、茎、叶和花中的表达量,而且AaHDR2在花中的表达量要明显高于叶中;MeJA和ABA能够大幅度上调AaHDR1AaHDR2的表达,而GA3仅能大幅度上调AaHDR2的表达。据AaHDR1AaHDR2的表达分析表明,AaHDR2对青蒿素在内的萜类物质的生物合成贡献更大,因此用AaHDR2进行后续的实验研究。生物信息学分析表明,AaHDR2属于HDR家族,进一步采用功能互补在E.coli突变体MG1655ara<>HDR中证明AaHDR2编码蛋白质的确具有HDR的功能。AaHDR2亚细胞定位结果显示:AaHDR2融合GFP蛋白特异性定位于叶绿体中,符合MEP途径定位于质体的事实。采用转基因技术在拟南芥中过表达AaHDR2能显著性提高叶绿素a、叶绿素b和类胡萝卜素含量。因此,本文所克隆的AaHDR2是利用代谢工程技术提高萜类物质生物合成能力的一个候选基因。

     

    Abstract: Artemisinin is the first choice for malaria treatment. The plastidial MEP pathway provides 5-carbon precursors (IPP and its isomer DMAPP) for the biosynthesis of isoprenoid (including artemisinin). Hydroxy-2-methyl-2-(E)-butenyl 4-diphosphate reductase (HDR) is the last enzyme involved in the MEP pathway, which catalyzes HMBPP to form IPP and DMAPP. In this study, we isolated the full-length cDNA of HDR from Artemisia annua L. (AaHDR2) and performed functional analysis. According to gene expression analysis of AaHDR2 (GenBank:KX058541) and AaHDR1 reported ever (GenBank:ADC84348.1) by qPCR, we found that AaHDR1 and AaHDR2 had much higher expression level in trichomes than that in roots, stems, leaves and flowers. AaHDR2 had much higher expression level in flowers than that in leaves. Further, the plant hormones such as MeJA and ABA respectively up-regulated the expression level of AaHDR1 and AaHDR2 significantly, but GA3 up-regulated the expression level of AaHDR2 only. The gene expression analysis of AaHDR1 and AaHDR2 showed that AaHDR2 had a greater contribution than AaHDR1 to isoprenoid biosynthesis (including artemisinin). We used AaHDR2 for the following experiments. Bioinformatic analysis indicated that AaHDR2 belonged to the HDR family and the functional complementation assay showed that AaHDR2 did have the enzymatic function of HDR, using E. coli mutant MG1655ara<>HDR as host cell. The subcellular localization assay showed that AaHDR2 fused with GFP at its N-terminal specifically targeted in chloroplasts. Finally, AaHDR2 was overexpressed in Arabidopsis thaliana. The AaHDR2-overexpressing plants produced the isoprenoids including chlorophyll a, chlorophyll b and carotenoids at significantly higher levels than the wild-type Arabidopsis plants. In summary, AaHDR2 might be a candidate gene for genetic improvement of the isoprenoid biosynthesis.

     

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