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转录组谱分析显示,甲基茉莉酸处理对西洋参不定根人参皂苷途径中基因调控模式的影响。

Transcriptome profiling shows gene regulation patterns in ginsenoside pathway in response to methyl jasmonate in Panax Quinquefolium adventitious root.

机构信息

Tianjin Key Laboratory for Modern Drug Delivery and High Efficiency, School of Pharmaceutical Science and Technology, Tianjin University, Tianjin 300072, China.

Key Laboratory of Systems Bioengineering, Ministry of Education, Tianjin University, Tianjin 300072, China.

出版信息

Sci Rep. 2016 Nov 23;6:37263. doi: 10.1038/srep37263.

Abstract

Here, we combine elicitors and transcriptomics to investigate the inducible biosynthesis of the ginsenoside from the Panax quinquefolium. Treatment of P. quinquefolium adventitious root with methyl jasmonate (MJ) results in an increase in ginsenoside content (43.66 mg/g compared to 8.32 mg/g in control group). Therefore, we sequenced the transcriptome of native and MJ treated adventitious root in order to elucidate the key differentially expressed genes (DEGs) in the ginsenoside biosynthetic pathway. Through DEG analysis, we found that 5,759 unigenes were up-regulated and 6,389 unigenes down-regulated in response to MJ treatment. Several defense-related genes (48) were identified, participating in salicylic acid (SA), jasmonic acid (JA), nitric oxide (NO) and abscisic acid (ABA) signal pathway. Additionally, we mapped 72 unigenes to the ginsenoside biosynthetic pathway. Four cytochrome P450s (CYP450) were likely to catalyze hydroxylation at C-16 (c15743_g1, c39772_g1, c55422_g1) and C-30 (c52011_g1) of the triterpene backbone. UDP-xylose synthases (c52571_g3) was selected as the candidate, which was likely to involve in ginsenoside Rb biosynthesis.

摘要

在这里,我们结合诱导子和转录组学来研究从西洋参中诱导产生人参皂苷。用茉莉酸甲酯(MJ)处理西洋参不定根会导致人参皂苷含量增加(与对照组的 8.32mg/g 相比为 43.66mg/g)。因此,我们对天然和 MJ 处理的不定根进行了转录组测序,以阐明人参皂苷生物合成途径中的关键差异表达基因(DEG)。通过 DEG 分析,我们发现 5759 个基因上调,6389 个基因下调对 MJ 处理的反应。鉴定出了几个与防御相关的基因(48 个),参与水杨酸(SA)、茉莉酸(JA)、一氧化氮(NO)和脱落酸(ABA)信号通路。此外,我们将 72 个基因映射到人参皂苷生物合成途径。四个细胞色素 P450(CYP450)可能催化三萜骨架 C-16(c15743_g1、c39772_g1、c55422_g1)和 C-30(c52011_g1)的羟化。UDP-木糖合成酶(c52571_g3)被选为候选基因,它可能参与人参皂苷 Rb 的生物合成。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/35c9/5120341/3882a2dc1397/srep37263-f1.jpg

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