Department of Biology, University of Erlangen-Nuremberg, 91058, Erlangen, Germany.
Plant Cell Rep. 2021 Sep;40(9):1631-1646. doi: 10.1007/s00299-021-02707-3. Epub 2021 Jun 19.
Studying RNAi-mediated DlP5βR1 and DlP5βR2 knockdown shoot culture lines of Digitalis lanata, we here provide direct evidence for the participation of PRISEs (progesterone 5β-reductase/iridoid synthase-like enzymes) in 5β-cardenolide formation. Progesterone 5β-reductases (P5βR) are assumed to catalyze the reduction of progesterone to 5β-pregnane-3,20-dione, which is a crucial step in the biosynthesis of the 5β-cardenolides. P5βRs are encoded by VEP1-like genes occurring ubiquitously in embryophytes. P5βRs are substrate-promiscuous enone-1,4-reductases recently termed PRISEs (progesterone 5β-reductase/iridoid synthase-like enzymes). Two PRISE genes, termed DlP5βR1 (AY585867.1) and DlP5βR2 (HM210089.1) were isolated from Digitalis lanata. To give experimental evidence for the participation of PRISEs in 5β-cardenolide formation, we here established several RNAi-mediated DlP5βR1 and DlP5βR2 knockdown shoot culture lines of D. lanata. Cardenolide contents were lower in D. lanata P5βR-RNAi lines than in wild-type shoots. We considered that the gene knockdowns may have had pleiotropic effects such as an increase in glutathione (GSH) which is known to inhibit cardenolide formation. GSH levels and expression of glutathione reductase (GR) were measured. Both were higher in the Dl P5βR-RNAi lines than in the wild-type shoots. Cardenolide biosynthesis was restored by buthionine sulfoximine (BSO) treatment in Dl P5βR2-RNAi lines but not in Dl P5βR1-RNAi lines. Since progesterone is a precursor of cardenolides but can also act as a reactive electrophile species (RES), we here discriminated between these by comparing the effects of progesterone and methyl vinyl ketone, a small RES but not a precursor of cardenolides. To the best of our knowledge, we here demonstrated for the first time that P5βR1 is involved in cardenolide formation. We also provide further evidence that PRISEs are also important for plants dealing with stress by detoxifying reactive electrophile species (RES).
我们通过研究毛地黄 DlP5βR1 和 DlP5βR2 敲低的 RNAi 茎培养物,为 PRISEs(孕酮 5β-还原酶/裂环环烯醚萜合酶样酶)参与 5β-卡烯内酯形成提供了直接证据。孕酮 5β-还原酶(P5βR)被认为可以催化孕酮转化为 5β-孕烷-3,20-二酮,这是 5β-卡烯内酯生物合成的关键步骤。P5βR 由普遍存在于胚胎植物中的 VEP1 样基因编码。P5βR 是底物杂化的烯酮 1,4-还原酶,最近被称为 PRISEs(孕酮 5β-还原酶/裂环环烯醚萜合酶样酶)。我们从毛地黄中分离出两个 PRISE 基因,称为 DlP5βR1(AY585867.1)和 DlP5βR2(HM210089.1)。为了提供 PRISEs 参与 5β-卡烯内酯形成的实验证据,我们在此建立了几个毛地黄的 DlP5βR1 和 DlP5βR2 RNAi 介导的茎培养物敲低系。与野生型茎相比,毛地黄 P5βR-RNAi 系中的卡烯内酯含量较低。我们认为基因敲低可能具有多效性效应,例如增加已知抑制卡烯内酯形成的谷胱甘肽(GSH)。测量了 GSH 水平和谷胱甘肽还原酶(GR)的表达。与野生型茎相比,这两种物质在 DlP5βR-RNAi 系中的含量都更高。在 DlP5βR2-RNAi 系中,用丁硫氨酸亚砜(BSO)处理可恢复卡烯内酯的生物合成,但在 DlP5βR1-RNAi 系中则不行。由于孕酮是卡烯内酯的前体,但也可以作为反应性亲电物质(RES),因此我们通过比较孕酮和甲基乙烯酮的效果来区分它们,甲基乙烯酮是一种小的 RES,但不是卡烯内酯的前体。据我们所知,我们首次证明 P5βR1 参与了卡烯内酯的形成。我们还提供了进一步的证据,表明 PRISEs 对于通过解毒反应性亲电物质(RES)来应对应激的植物也很重要。