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UV-B 诱导黄花蒿黄酮类化合物积累的表观遗传调控

Epigenetic control of UV-B-induced flavonoid accumulation in Artemisia annua L.

机构信息

Department of Botany, Institute of Science, Banaras Hindu University, Varanasi, India.

Department of Botany, CMP Degree College, University of Allahabad, Allahabad, India.

出版信息

Planta. 2019 Feb;249(2):497-514. doi: 10.1007/s00425-018-3022-7. Epub 2018 Sep 28.

Abstract

UV-B-induced flavonoid biosynthesis is epigenetically regulated by site-specific demethylation of AaMYB1, AaMYC, and AaWRKY TF-binding sites inAaPAL1promoter-causing overexpression ofAaPALgene inArtemisia annua. The present study was undertaken to understand the epigenetic regulation of flavonoid biosynthesis under the influence of ultraviolet-B radiation using Artemisia annua L. as an experimental model. In-vitro propagated and acclimatized plantlets were treated with UV-B radiation (2.8 W m; 3 h), which resulted in enhanced accumulation of total flavonoid and phenolics content as well as eleven individual flavonoids measured through HPLC-DAC. Expression of eight genes (phenylanaline ammonia lyase, cinnamate-4-hydroxylase, 4-coumarate: CoA ligase; chalcone synthase, chalcone isomerase, cinnamoyl reductase, flavonoid-3'-hydroxylase, and flavones synthase) from upstream and downstream flavonoid biosynthetic pathways was measured through RT-PCR and RT-Q-PCR and all were variably induced under UV-B irradiation. Among them, AaPAL1 transcript and its protein were most significantly upregulated. Global DNA methylation analysis revealed hypomethylation of genomic DNA in A. annua. Further epigenetic characterization of promoter region of AaPAL1 revealed cytosine demethylation at five sites, which in turn caused epigenetic activation of six transcription factor-binding sites including QELEMENT, EBOXBNNAPA/MYCCONSENSUSAT, MYBCORE, MYBCOREATCYCB1, and GCCCORE. MYB transcription factors are positive regulators of flavonoid biosynthesis. Epigenetic activation of transcription-enhancing cis-regulatory elements in AaPAL1 promoter and subsequent overexpression of AaMYB1 and AaMYC and AaWRKY transcription factors under UV-B irradiation may probably be the reason for higher AaPAL1 expression and hence greater biosynthesis of flavonoids in A. annua L. The present study is the first report that provides mechanistic evidence of epigenetic regulation of flavonoid biosynthesis under UV-B radiation in A. annua L.

摘要

UV-B 诱导的类黄酮生物合成是通过 AaPAL1 启动子中 AaMYB1、AaMYC 和 AaWRKY TF 结合位点的特异性去甲基化来进行表观遗传调控的,导致 AaPAL 基因的过表达,从而在青蒿中过量表达。本研究以黄花蒿(Artemisia annua L.)为实验模型,探讨了紫外-B 辐射影响下类黄酮生物合成的表观遗传调控机制。对离体繁殖和驯化的植物进行了 UV-B 辐射(2.8 W m; 3 h)处理,导致总类黄酮和酚类含量以及通过 HPLC-DAC 测量的 11 种单个类黄酮的积累增加。通过 RT-PCR 和 RT-Q-PCR 测量了上游和下游类黄酮生物合成途径的 8 个基因(苯丙氨酸氨裂解酶、肉桂酸-4-羟化酶、4-香豆酸:CoA 连接酶;查尔酮合酶、查尔酮异构酶、肉桂酰还原酶、黄酮-3'-羟化酶和黄酮合酶)的表达,所有基因在 UV-B 照射下均有不同程度的诱导。其中,AaPAL1 转录本及其蛋白表达水平显著上调。全基因组 DNA 甲基化分析显示黄花蒿基因组 DNA 去甲基化。进一步对 AaPAL1 启动子区的表观遗传学特征进行分析,发现五个位点的胞嘧啶去甲基化,进而导致包括 QELEMENT、EBOXBNNAPA/MYCCONSENSUSAT、MYBCORE、MYBCOREATCYCB1 和 GCCCORE 在内的六个转录因子结合位点的表观遗传激活。MYB 转录因子是类黄酮生物合成的正调控因子。在 UV-B 照射下,AaPAL1 启动子中增强转录的顺式调控元件的表观遗传激活,以及随后 AaMYB1、AaMYC 和 AaWRKY 转录因子的过表达,可能是 AaPAL1 表达增加和青蒿中类黄酮生物合成增加的原因。本研究首次提供了黄花蒿中 UV-B 辐射下类黄酮生物合成的表观遗传调控机制的证据。

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