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蒙古黄芪根的转录组测序与特征分析揭示了参与黄酮类生物合成的关键基因。

Transcriptome sequencing and characterization of Astragalus membranaceus var. mongholicus root reveals key genes involved in flavonoids biosynthesis.

作者信息

Liang Jianping, Li Wenqian, Jia Xiaoyun, Zhang Ying, Zhao Jianping

机构信息

Department of Life Science, Shanxi Agricultural University, Taigu, 030801, Shanxi, China.

Experiment mangement center, Shanxi University of Chinese Medicine, Jinzhong, 030619, Shanxi, China.

出版信息

Genes Genomics. 2020 Aug;42(8):901-914. doi: 10.1007/s13258-020-00953-5. Epub 2020 Jun 9.

Abstract

BACKGROUND

Astragalus membranaceus (Fisch.) Bge. var. mongholicus (Bge.) Hsiao is a traditional medicinal herb of Leguminosae since it contains bioactive compounds such as flavonoids, which have significant pharmacological effects on immunity and antioxidant. However, the scanty genomic and transcriptome resources of Astragalus membranaceus have hindered further exploration of its biosynthesis and accumulation mechanism.

OBJECTIVE

This project aim to further improve our understanding of the relationship between transcriptional behavior and flavonoids content of A. mongholicus.

METHODS

The accumulation of flavonoids and related gene expression in five different developmental stages (A: vegetative, B: florescence, C: fruiting, D: fruit ripening and E: defoliating stages) of A. mongholicus root were studied by combining UV spectrophotometry and transcriptomic techniques. The de novo assembly, annotation and functional evaluation of the contigs were performed with bioinformatics tools.

RESULTS

After screening and assembling the raw data, there were a total of 158,123 unigenes with an average length of 644.89 bp were finally obtained, which has 8362 unigenes could be jointly annotated by NR, SwissProt, eggNOG, GO, KEGG and Pfam databases. KEGG enrichment analysis was performed on differentially expressed genes(DEGs)in the four groups (A vs. B, B vs. C, C vs. D, D vs. E). The results showed that many DEGs in each group were significantly enriched to flavonoids biosynthesis related pathways. Among them, a number of 86 were involved in the biosynthesis of isoflavonoid (12), flavonoid (5) and phenylpropanoid (69). Further analysis of these DEGs revealed that the expression levels of key genes such as PAL, 4CL, CCR, COMT, DFR, etc. were all down-regulated at the fruiting stage, and then raised at the fruit ripening stage. This expression pattern was similar to the accumulation trend of total flavonoids content.

CONCLUSIONS

In summary, this comprehensive transcriptome dataset allowed the identification of genes associated with flavonoids metabolic pathways. The results laid a foundation for the biosynthesis and regulation of flavonoids. It also provided a scientific basis for the most suitable harvest time and resource utilization of A. mongholicus.

摘要

背景

蒙古黄芪是豆科的一种传统药用植物,因为它含有黄酮类等生物活性化合物,这些化合物对免疫和抗氧化具有显著的药理作用。然而,蒙古黄芪稀少的基因组和转录组资源阻碍了对其生物合成和积累机制的进一步探索。

目的

本项目旨在进一步加深我们对蒙古黄芪转录行为与黄酮类化合物含量之间关系的理解。

方法

结合紫外分光光度法和转录组技术,研究蒙古黄芪根在五个不同发育阶段(A:营养期、B:花期、C:结果期、D:果实成熟期、E:落叶期)黄酮类化合物的积累及相关基因表达。利用生物信息学工具对重叠群进行从头组装、注释和功能评估。

结果

对原始数据进行筛选和组装后,最终共获得158,123个单基因,平均长度为644.89 bp,其中有8362个单基因可被NR、SwissProt、eggNOG、GO、KEGG和Pfam数据库联合注释。对四组(A组与B组、B组与C组、C组与D组、D组与E组)差异表达基因(DEG)进行KEGG富集分析。结果表明,每组中的许多DEG都显著富集到黄酮类生物合成相关途径。其中,有86个参与异黄酮(12个)、黄酮(5个)和苯丙烷类(69个)的生物合成。对这些DEG的进一步分析表明,PAL、4CL、CCR、COMT、DFR等关键基因的表达水平在结果期均下调,然后在果实成熟期升高。这种表达模式与总黄酮含量的积累趋势相似。

结论

综上所述,这个综合转录组数据集有助于鉴定与黄酮类代谢途径相关的基因。研究结果为黄酮类化合物的生物合成和调控奠定了基础。它也为蒙古黄芪最合适的收获时间和资源利用提供了科学依据。

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