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通过表达一种修饰的HMG-CoA还原酶增强种子植物甾醇积累

Enhanced seed phytosterol accumulation through expression of a modified HMG-CoA reductase.

作者信息

Hey Sandra J, Powers Stephen J, Beale Michael H, Hawkins Nathaniel D, Ward Jane L, Halford Nigel G

机构信息

Crop Performance and Improvement, Rothamsted Research, Harpenden, Hertfordshire AL5 2JQ, UK.

出版信息

Plant Biotechnol J. 2006 Mar;4(2):219-29. doi: 10.1111/j.1467-7652.2005.00174.x.

Abstract

The regulation of phytosterol biosynthesis in seeds is of interest to biotechnologists because of the efficacy of dietary phytosterols in reducing blood cholesterol in humans. Mevalonate synthesis via 3-hydroxy-3-methylglutaryl-coenzyme A reductase (HMG-CoA reductase) is a key step in phytosterol biosynthesis. HMG-CoA reductase is inactivated by phosphorylation by SNF1-related protein kinase 1 (SnRK1). With the aim of increasing seed phytosterol levels, transgenic tobacco plants were produced expressing a full-length Arabidopsis (Arabidopsis thaliana) HMG-CoA reductase gene (HMG1) coding sequence, a modified HMG1 sequence encoding a protein lacking the target serine residue for phosphorylation by SnRK1, or a chimaeric sequence encoding the N-terminal domain of the Arabidopsis HMG1 enzyme fused with the catalytic domain of yeast HMG-CoA reductase, which lacks an SnRK1 target site. All three transgenes (35S-AtHMG1, 35S-AtHMG1m and 35S-AtScHMG1) were under the control of a cauliflower mosaic virus 35S RNA promoter. Levels of seed phytosterols were up to 2.44-fold higher in plants transformed with the 35S-AtHMG1m gene than in the wild-type, and were significantly higher than in plants expressing 35S-AtHMG1 or 35S-AtScHMG1. In contrast, levels of phytosterols in leaves of plants transformed with the 35S-AtHMG1m gene were unchanged, suggesting that regulation of HMG-CoA reductase by SnRK1 is an important factor in seeds but not in leaves. A total of 11 independent transgenic lines expressing 35S-AtHMG1m or 35S-AtScHMG1 also showed an altered flower phenotype, comprising a compact floret, prolonged flowering, short, pale petals, a protruding style, short stamens, late anther development, little or no pollen production, premature flower abscission and poor seed set. Because of this phenotype, the modified HMG-CoA reductase gene would have to be expressed seed specifically if it were to be engineered into a crop plant for biotechnological purposes.

摘要

由于膳食植物甾醇在降低人体血液胆固醇方面的功效,种子中植物甾醇生物合成的调控引起了生物技术专家的兴趣。通过3-羟基-3-甲基戊二酰辅酶A还原酶(HMG-CoA还原酶)合成甲羟戊酸是植物甾醇生物合成的关键步骤。HMG-CoA还原酶被SNF1相关蛋白激酶1(SnRK1)磷酸化而失活。为了提高种子中植物甾醇的水平,培育了表达全长拟南芥(Arabidopsis thaliana)HMG-CoA还原酶基因(HMG1)编码序列、编码缺乏被SnRK1磷酸化的目标丝氨酸残基的蛋白质的修饰HMG1序列或编码与酵母HMG-CoA还原酶催化结构域融合的拟南芥HMG1酶N端结构域的嵌合序列的转基因烟草植株。所有三个转基因(35S-AtHMG1、35S-AtHMG1m和35S-AtScHMG1)都受花椰菜花叶病毒35S RNA启动子的控制。用35S-AtHMG1m基因转化的植株种子中植物甾醇水平比野生型高2.44倍,且显著高于表达35S-AtHMG1或35S-AtScHMG1的植株。相反,用35S-AtHMG1m基因转化的植株叶片中植物甾醇水平未改变,这表明SnRK1对HMG-CoA还原酶的调控在种子中是一个重要因素,而在叶片中不是。总共11个表达35S-AtHMG1m或35S-AtScHMG1的独立转基因株系也表现出花表型改变,包括小花紧凑、花期延长、花瓣短而苍白、花柱突出、雄蕊短、花药发育延迟、很少或不产生花粉、花过早脱落和结实率低。由于这种表型,如果要将修饰的HMG-CoA还原酶基因用于生物技术目的而导入作物植株中,就必须在种子中特异性表达。

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