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组蛋白 H3K4 和 H3K9 甲基化调控金银花中绿原酸、黄酮和环烯醚萜苷生物合成。

Regulation of chlorogenic acid, flavonoid, and iridoid biosynthesis by histone H3K4 and H3K9 methylation in Lonicera japonica.

机构信息

State Key Laboratory of Dao-Di Herbs, National Resource Center for Chinese Materia Medica, China Academy of Chinese Medical Sciences, Beijing, 100700, People's Republic of China.

出版信息

Mol Biol Rep. 2020 Dec;47(12):9301-9311. doi: 10.1007/s11033-020-05990-7. Epub 2020 Nov 15.

Abstract

Lonicera japonica is used in Chinese herbal medicines with a wide spectrum of pharmacological properties associated with chlorogenic acid, flavonoid and iridoid. The biosynthesis of these compounds could be affected by genetic inheritance and epigenetic modification. However, the mechanisms that regulate the expression of genes involved in the biosynthesis of these compounds are rarely known. The results of qRT-PCR showed that the biosynthesis gene expression of these compounds was related to histone H3K4 and H3K9 methylation levels. These active compounds content of L. japonica were measured by UPLC-MS/MS. H3K4me3 showed a positive correlation with chlorogenic acid and loganic acid content, and H3K9me positively correlated with luteolin content. The correlation between histone methylation levels and the levels of luteolin and loganic acid in L. japonica from different producing areas validate the regulatory role of histone methylation in biosynthesis of bioactive compounds. Our study demonstrated a potential regulatory network of H3K9/H3K4 methylation to gene expression and content of secondary metabolites, and provided a basis for understanding the mechanism underlying the variation of major bioactive compounds in L. japonica.

摘要

忍冬在中药中有广泛的药理作用,与绿原酸、黄酮类和环烯醚萜有关。这些化合物的生物合成可能受到遗传和表观遗传修饰的影响。然而,调节这些化合物生物合成相关基因表达的机制却鲜为人知。qRT-PCR 的结果表明,这些化合物的生物合成基因表达与组蛋白 H3K4 和 H3K9 甲基化水平有关。采用 UPLC-MS/MS 测定了忍冬中这些活性化合物的含量。H3K4me3 与绿原酸和马钱酸loganin 含量呈正相关,H3K9me 与木犀草素含量呈正相关。不同产地忍冬中组蛋白甲基化水平与木犀草素和马钱酸 loganin 含量的相关性验证了组蛋白甲基化在生物活性化合物生物合成中的调节作用。本研究揭示了 H3K9/H3K4 甲基化对次生代谢产物基因表达和含量的潜在调控网络,为理解忍冬中主要生物活性化合物变异的机制提供了依据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/865f/7666716/bc4f429f0ffa/11033_2020_5990_Fig1_HTML.jpg

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