DBR2样启动子变异影响不同化学型青蒿中青蒿素的产生。

IF 7.6 Q1 GENETICS & HEREDITY 园艺研究(英文) Pub Date : 2023-08-16 eCollection Date: 2023-09-01 DOI:10.1093/hr/uhad164
Xingwen Wang, Lan Wu, Li Xiang, Ranran Gao, Qinggang Yin, Mengyue Wang, Zhaoyu Liu, Liang Leng, Yanyan Su, Huihua Wan, Tingyu Ma, Shilin Chen, Yuhua Shi
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摘要

青蒿是唯一已知的强效抗疟青蒿素的植物来源,它以产生低和高青蒿素(LAP和HAP)的化学型出现。尽管如此,这两种化学型产生青蒿素的不同机制仍不完全清楚。在这里,我们对基因组重测序、代谢组和转录组数据进行了全面分析,以系统地比较LAP化学型JL和HAP化学型HAN的差异。代谢产物分析显示,与JL相比,HAN中72.18%的倍半萜高度积累。综合组学分析发现,一个类似DBR2L的基因可能参与青蒿素的生物合成。DBR2L与DBR2高度同源,属于ORR3家族,具有催化卤醛生成二氢卤醛的DBR2活性。基因组重测序和启动子克隆结果表明,不同品种的A.annua的DBR2L启动子存在复杂的变异,可分为三种变异类型。不同变体类型的启动子活性存在明显差异。此外,还鉴定了DBR2L启动子的核心区域(-625至0),并筛选了参与DBR2L调控的候选转录因子。因此,结果表明DBR2L是参与青蒿素生物合成的另一个关键酶。DBR2L的启动子变异影响其表达水平,从而可能导致青蒿品种中青蒿素的产量不同。它为青蒿素在a.annua的LAP和HAP化学型中产生差异的机制提供了新的见解,并将有助于a.annua中青蒿素的高产。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Promoter variations in DBR2-like affect artemisinin production in different chemotypes of Artemisia annua.

Artemisia annua is the only known plant source of the potent antimalarial artemisinin, which occurs as the low- and high-artemisinin producing (LAP and HAP) chemotypes. Nevertheless, the different mechanisms of artemisinin producing between these two chemotypes were still not fully understood. Here, we performed a comprehensive analysis of genome resequencing, metabolome, and transcriptome data to systematically compare the difference in the LAP chemotype JL and HAP chemotype HAN. Metabolites analysis revealed that 72.18% of sesquiterpenes was highly accumulated in HAN compared to JL. Integrated omics analysis found a DBR2-Like (DBR2L) gene may be involved in artemisinin biosynthesis. DBR2L was highly homologous with DBR2, belonged to ORR3 family, and had the DBR2 activity of catalyzing artemisinic aldehyde to dihydroartemisinic aldehyde. Genome resequencing and promoter cloning revealed that complicated variations existed in DBR2L promoters among different varieties of A. annua and were clustered into three variation types. The promoter activity of diverse variant types showed obvious differences. Furthermore, the core region (-625 to 0) of the DBR2L promoter was identified and candidate transcription factors involved in DBR2L regulation were screened. Thus, the result indicates that DBR2L is another key enzyme involved in artemisinin biosynthesis. The promoter variation in DBR2L affects its expression level, and thereby may result in the different yield of artemisinin in varieties of A. annua. It provides a novel insight into the mechanism of artemisinin-producing difference in LAP and HAP chemotypes of A. annua, and will assist in a high yield of artemisinin in A. annua.

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