首页> 美国卫生研究院文献>PLoS Clinical Trials >Plant Sterol Metabolism. Δ7-Sterol-C5-Desaturase (STE1/DWARF7), Δ5,7-Sterol-Δ7-Reductase (DWARF5) and Δ24-Sterol-Δ24-Reductase (DIMINUTO/DWARF1) Show Multiple Subcellular Localizations in Arabidopsis thaliana (Heynh) L
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Plant Sterol Metabolism. Δ7-Sterol-C5-Desaturase (STE1/DWARF7), Δ5,7-Sterol-Δ7-Reductase (DWARF5) and Δ24-Sterol-Δ24-Reductase (DIMINUTO/DWARF1) Show Multiple Subcellular Localizations in Arabidopsis thaliana (Heynh) L

机译:植物甾醇代谢。 Δ7-Sterol-C5-去饱和酶(STE1 / DWARF7),Δ5,7-Sterol-Δ7-还原酶(DWARF5)和Δ24-Sterol-Δ24-还原酶(DIMINUTO / DWARF1)显示拟南芥(Heynh)L中的多个亚细胞定位

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摘要

Sterols are crucial lipid components that regulate membrane permeability and fluidity and are the precursors of bioactive steroids. The plant sterols exist as three major forms, free sterols, steryl glycosides and steryl esters. The storage of steryl esters in lipid droplets has been shown to contribute to cellular sterol homeostasis. To further document cellular aspects of sterol biosynthesis in plants, we addressed the question of the subcellular localization of the enzymes implicated in the final steps of the post-squalene biosynthetic pathway. In order to create a clear localization map of steroidogenic enzymes in cells, the coding regions of Δ7-sterol-C5-desaturase (STE1/DWARF7), Δ24-sterol-Δ24-reductase (DIMINUTO/DWARF1) and Δ5,7-sterol-Δ7-reductase (DWARF5) were fused to the yellow fluorescent protein (YFP) and transformed into Arabidopsis thaliana mutant lines deficient in the corresponding enzymes. All fusion proteins were found to localize in the endoplasmic reticulum in functionally complemented plants. The results show that both Δ5,7-sterol-Δ7-reductase and Δ24-sterol-Δ24-reductase are in addition localized to the plasma membrane, whereas Δ7-sterol-C5-desaturase was clearly detected in lipid particles. These findings raise new challenging questions about the spatial and dynamic cellular organization of sterol biosynthesis in plants.
机译:甾醇是调节膜通透性和流动性的关键脂质成分,是生物活性甾体的前体。植物固醇以三种主要形式存在:游离固醇,固醇糖苷和固醇酯。脂滴中甾醇酯的储存已显示有助于细胞固醇稳态。为了进一步记录植物中固醇生物合成的细胞方面,我们研究了角鲨烯后生物合成途径的最终步骤所牵涉的酶的亚细胞定位问题。为了建立清晰的类固醇生成酶在细胞中的定位图,Δ 7 -甾醇-C5-去饱和酶(STE1 / DWARF7),Δ 24 -固醇的编码区-Δ 24 -还原酶(DIMINUTO / DWARF1)和Δ 5,7 -甾醇-Δ 7 -还原酶(DWARF5)与黄色荧光蛋白(YFP),并转化为缺乏相应酶的拟南芥突变株。发现所有融合蛋白都定位在功能互补的植物的内质网中。结果表明,Δ 5,7 -甾醇-Δ 7 -还原酶和Δ 24 -甾醇-Δ 24 -还原酶位于质膜上,而在脂质颗粒中清楚地检测到了Δ 7 -甾醇-C5-去饱和酶。这些发现提出了关于植物中固醇生物合成的空间和动态细胞组织的新挑战性问题。

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