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GmFNSII调控的大豆黄酮代谢对非生物胁迫作出响应并调节植物耐盐性。

GmFNSII-controlled soybean flavone metabolism responds to abiotic stresses and regulates plant salt tolerance.

作者信息

Yan Junhui, Wang Biao, Jiang Yina, Cheng Linjing, Wu Tianlong

机构信息

Key Laboratory of Urban Agriculture (South) Ministry of Agriculture, School of Agriculture and Biology, Shanghai Jiao Tong University, No. 800 Dongchuan Rd., Shanghai, PR China 200240.

出版信息

Plant Cell Physiol. 2014 Jan;55(1):74-86. doi: 10.1093/pcp/pct159. Epub 2013 Nov 4.

Abstract

Flavones, a major group of flavonoids in most plant tissues, play multiple roles in plant-environment interactions. In our study, the expression of the two soybean flavone synthase genes, GmFNSII-1 and GmFNSII-2, was significantly increased by methyl jasmonate (MeJA), glucose, mannitol and NaCl treatment, which were also found to increase flavone aglycone accumulation in Glycine max (L.) Merrill. In the GmFNSII-1 promoter, a specific CGTCA motif in the region (-979 bp to -806 bp) involved in the MeJA response was identified. Promoter deletion analysis of GmFNSII-2 revealed the presence of osmotic-responsive (-1,143 bp to -767 bp) and glucose-repressive sequence elements (-767 bp to -475 bp), which strongly supported the hypothesis that glucose induces soybean flavone production by acting as both an osmotic factor and a sugar signaling molecule simultaneously. Silencing of the GmFNSII gene clearly reduced the production of flavone aglycones (apigenin, luteolin and 7,4'-dihydroxyflavone) in hairy roots. The GmFNSII-RNAi (RNA interference) roots that had a reduced level of flavones accompanied by more malondialdehyde and H2O2 accumulation were more sensitive to salt stress compared with those of the control, and we concluded that flavones, as antioxidants, are associated with salt tolerance.

摘要

黄酮类化合物是大多数植物组织中黄酮类的主要组成部分,在植物与环境的相互作用中发挥多种作用。在我们的研究中,两种大豆黄酮合酶基因GmFNSII - 1和GmFNSII - 2的表达在茉莉酸甲酯(MeJA)、葡萄糖、甘露醇和NaCl处理后显著增加,这些处理还能增加大豆(Glycine max (L.) Merrill)中黄酮苷元的积累。在GmFNSII - 1启动子中,鉴定出了一个位于(-979 bp至-806 bp)区域内参与MeJA应答的特定CGTCA基序。对GmFNSII - 2的启动子缺失分析揭示了渗透应答序列元件(-1,143 bp至-767 bp)和葡萄糖抑制序列元件(-767 bp至-475 bp)的存在,这有力地支持了葡萄糖同时作为渗透因子和糖信号分子诱导大豆黄酮生成的假说。沉默GmFNSII基因明显降低了毛状根中黄酮苷元(芹菜素、木犀草素和7,4'-二羟基黄酮)的生成。与对照相比,黄酮水平降低且丙二醛和H2O2积累更多的GmFNSII - RNAi(RNA干扰)根对盐胁迫更敏感,我们得出结论,黄酮作为抗氧化剂与耐盐性有关。

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