首页> 外文期刊>American Journal of Plant Sciences >Cloning, Expression Pattern Analysis and Subcellular Localization of Resveratrol Synthase Gene in Peanut (Arachis hypogaea L.)
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Cloning, Expression Pattern Analysis and Subcellular Localization of Resveratrol Synthase Gene in Peanut (Arachis hypogaea L.)

机译:白藜芦醇合酶基因在花生中的克隆,表达模式分析及亚细胞定位

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Resveratrol synthase (RS) is a key enzyme that plays a critical role in the resveratrol synthesis pathway. In this study, six RS genes were isolated and characterized from peanut variety “Zhenzhu Hong” by silico cloning and RT-PCR. Bioinformatics analysis showed that deduced amino acid sequences of the six cloned RS genes were highly conserved with a similarity from 95% to 99% when compared to the RS genes which had been deposited at the GenBank. The results of amino acid sequences analysis showed six RS proteins contained the Chal_Sti_Synt_N and ACP_Syn_III_C domains and can be classified to same family but with different evolutionary distance. Expression pattern analysis by QRT-PCR provided evidence indicating that the mRNA of six RS genes were primarily expressed in the peanut shell at different developmental stages with different expression levels, but only lower levels of them were evident in the peanut kernel. The subcellular localization of RS protein in onion epidermal cell was performed by Agrobacterium tumefaciens-mediated transformation and the green fluorescent was monitored by confocal fluorescence microscopy. The results indicated that, RS1 and RS5 were located in the nucleus and plasma membrane respectively, while the RS2, RS3, RS4 and RS6 were located in both nucleus inner membrane and plasma membrane. The data will provide basic information for elucidating the regulatory mechanisms and enzyme kinetics underlying the RS genes in the resveratrol synthase pathway.
机译:白藜芦醇合酶(RS)是一种关键酶,在白藜芦醇合成途径中起着至关重要的作用。在这项研究中,通过计算机克隆和RT-PCR从花生品种“珍竹红”中分离并鉴定了六个RS基因。生物信息学分析表明,与已保存在GenBank中的RS基因相比,六个克隆的RS基因的推导氨基酸序列高度保守,相似性从95%到99%。氨基酸序列分析结果表明,六个RS蛋白包含Chal_Sti_Synt_N和ACP_Syn_III_C结构域,可以分为同一家族,但进化距离不同。通过QRT-PCR的表达模式分析提供了证据,表明六个RS基因的mRNA主要在花生壳中以不同的发育水平和不同的表达水平表达,但在花生仁中只有较低的水平。通过根癌农杆菌介导的转化进行洋葱表皮细胞中RS蛋白的亚细胞定位,并通过共聚焦荧光显微镜监测绿色荧光。结果表明,RS1和RS5分别位于细胞核和质膜中,而RS2,RS3,RS4和RS6位于细胞核内膜和质膜中。该数据将提供基本信息,阐明白藜芦醇合酶途径中RS基因的调控机制和酶动力学。

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