首页> 外文期刊>Phytochemistry >Regulation of ginsenoside and phytosterol biosynthesis by RNA interferences of squalene epoxidase gene in Panax ginseng.
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Regulation of ginsenoside and phytosterol biosynthesis by RNA interferences of squalene epoxidase gene in Panax ginseng.

机译:人参中角鲨烯环氧酶基因的RNA干扰对人参皂苷和植物甾醇生物合成的调控。

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摘要

Squalene epoxidase catalyzes the first oxygenation step in phytosterol and triterpenoid saponin biosynthesis and is suggested to represent one of the rate-limiting enzymes in this pathway. Here, we investigated the roles of two squalene epoxidase genes (PgSQE1 and PgSQE2) in triterpene and phytosterol biosynthesis in Panax ginseng. PgSQE1 and PgSQE2 encoded deduced proteins of 537 and 545 amino acids, respectively. Amino acid sequences deduced from PgSQE1 and PgSQE2 share 83% homology, but the N-terminal regions (first 60 amino acids) are highly different. PgSQE1 mRNA abundantly accumulated in all organs. PgSQE2 was only weakly expressed and preferentially in petioles and flower buds. Methyl jasmonate (MeJA) treatment enhanced the accumulation of PgSQE1 mRNA in roots, but rather suppressed expression of PgSQE2. Precursor (squalene) treatment coordinately upregulated the expression of both PgSQE1 and PgSQE2. In situ hybridization analysis established that both PgSQE1 and PgSQE2 mRNAs accumulated preferentially in vascular bundle tissue and resin ducts of petioles. RNA interference of PgSQE1 in transgenic P. ginseng completely suppressed PgSQE1 transcription. Concomitantly, the interference of PgSQE1 resulted in reduction of ginsenoside production. Interestingly, silencing of PgSQE1 in RNAi roots strongly upregulated PgSQE2 and PNX (cycloartenol synthase) and resulted in enhanced phytosterol accumulation. These results indicate that expression of PgSQE1 and PgSQE2 were regulated in a different manner, and that PgSQE1 will regulate ginsenoside biosynthesis, but not that of phytosterols in P. ginseng
机译:角鲨烯环氧酶催化植物甾醇和三萜皂苷生物合成中的第一个氧化步骤,并被认为是该途径中的限速酶之一。在这里,我们调查了人参中三萜烯和植物甾醇的生物合成中两个角鲨烯环氧酶基因(PgSQE1和PgSQE2)的作用。 PgSQE1和PgSQE2分别编码537和545个氨基酸的推导蛋白。从PgSQE1和PgSQE2推导的氨基酸序列具有83%的同源性,但N端区域(前60个氨基酸)有很大差异。 PgSQE1 mRNA大量积累在所有器官中。 PgSQE2仅在叶柄和花蕾中弱表达,优先表达。茉莉酸甲酯(MeJA)处理增强了PgSQE1 mRNA在根中的积累,但抑制了PgSQE2的表达。前体(角鲨烯)处理可协同上调PgSQE1和PgSQE2的表达。原位杂交分析表明,PgSQE1和PgSQE2 mRNA均优先在叶柄的维管束组织和树脂管中积累。 PgSQE1在人参转基因植物中的RNA干扰完全抑制了PgSQE1的转录。同时,PgSQE1的干扰导致人参皂甙产量的减少。有趣的是,沉默RNAi根中的PgSQE1会强烈上调PgSQE2和PNX(环烯醇合成酶)并导致植物甾醇的积累增加。这些结果表明PgSQE1和PgSQE2的表达以不同的方式调节,并且PgSQE1将调节人参皂苷的生物合成,但不调节人参中的植物甾醇。

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