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在颠茄生物合成和根系生长中,两个精氨酸脱羧酶基因的功能分化。

Functional divergence of two arginine decarboxylase genes in tropane alkaloid biosynthesis and root growth in Atropa belladonna.

机构信息

Integrative Science Center of Germplasm Creation in Western China (CHONGQING) Science City, SWU-TAAHC Medicinal Plant Joint R&D Centre, School of Life Sciences, Southwest University, Chongqing 400715, China.

Key Laboratory of Synthetic Biology of Ministry of Agriculture and Rural Affairs, Tobacco Research Institute of Chinese Academy of Agricultural Sciences, Qingdao 266101, China.

出版信息

Plant Physiol Biochem. 2024 Mar;208:108439. doi: 10.1016/j.plaphy.2024.108439. Epub 2024 Feb 21.

Abstract

Putrescine, produced via the arginine decarboxylase (ADC)/ornithine decarboxylase (ODC)-mediated pathway, is an initial precursor for polyamines metabolism and the root-specific biosynthesis of medicinal tropane alkaloids (TAs). These alkaloids are widely used as muscarinic acetylcholine antagonists in clinics. Although the functions of ODC in biosynthesis of polyamines and TAs have been well investigated, the role of ADC is still poorly understood. In this study, enzyme inhibitor treatment showed that ADC was involved in the biosynthesis of putrescine-derived metabolites and root growth in Atropa belladonna. Further analysis found that there were six ADC unigenes in the A. belladonna transcriptome, with two of them, AbADC1 and AbADC2, exhibiting high expression in the roots. To investigate their roles in TAs/polyamines metabolism and root growth, RNA interference (RNAi) was used to suppress either AbADC1 or AbADC2 expression in A. belladonna hairy roots. Suppression of the AbADC1 expression resulted in a significant reduction in the putrescine content and hairy root biomass. However, it had no noticeable effect on the levels of N-methylputrescine and the TAs hyoscyamine, anisodamine, and scopolamine. On the other hand, suppression of AbADC2 expression markedly reduced the levels of putrescine, N-methylputrescine, and TAs, but had no significant effect on hairy root biomass. According to β-glucuronidase (GUS) staining assays, AbADC1 was mainly expressed in the root elongation and division region while AbADC2 was mainly expressed in the cylinder of the root maturation region. These differences in expression led to functional divergence, with AbADC1 primarily regulating root growth and AbADC2 contributing to TA biosynthesis.

摘要

腐胺通过精氨酸脱羧酶(ADC)/鸟氨酸脱羧酶(ODC)介导的途径产生,是多胺代谢和药用托烷生物碱(TAs)根特异性生物合成的初始前体。这些生物碱在临床上被广泛用作毒蕈碱乙酰胆碱拮抗剂。尽管 ODC 在多胺和 TAs 生物合成中的功能已得到很好的研究,但 ADC 的作用仍知之甚少。在这项研究中,酶抑制剂处理表明 ADC 参与了颠茄生物合成腐胺衍生代谢物和根系生长。进一步的分析发现,颠茄转录组中有六个 ADC 基因,其中 AbADC1 和 AbADC2 两个基因在根中表达量较高。为了研究它们在 TAs/多胺代谢和根系生长中的作用,使用 RNA 干扰(RNAi)抑制 AbADC1 或 AbADC2 在颠茄毛状根中的表达。抑制 AbADC1 的表达导致腐胺含量和毛状根生物量显著降低。然而,它对 N-甲基腐胺和 TAs 莨菪碱、山莨菪碱和东莨菪碱的水平没有明显影响。另一方面,抑制 AbADC2 的表达显著降低了腐胺、N-甲基腐胺和 TAs 的水平,但对毛状根生物量没有显著影响。根据β-葡萄糖醛酸酶(GUS)染色分析,AbADC1 主要在根伸长和分裂区表达,而 AbADC2 主要在根成熟区的圆柱区表达。这种表达上的差异导致了功能上的分化,AbADC1 主要调节根的生长,而 AbADC2 则有助于 TAs 的生物合成。

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