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RNAi-Mediated Tocopherol Deficiency Impairs Photoassimilate Export in Transgenic Potato Plants

机译:RNAi介导的生育酚缺乏会影响转基因马铃薯植株的光同化出口。

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摘要

Tocopherols (vitamin E) are lipophilic antioxidants presumed to play a key role in protecting chloroplast membranes and the photosynthetic apparatus from photooxidative damage. Additional nonantioxidant functions of tocopherols have been proposed after the recent finding that the Suc export defective1 maize (Zea mays) mutant (sxd1) carries a defect in tocopherol cyclase (TC) and thus is devoid of tocopherols. However, the corresponding vitamin E deficient1 Arabidopsis mutant (vte1) lacks a phenotype analogous to sxd1, suggesting differences in tocopherol function between C4 and C3 plants. Therefore, in this study, the potato (Solanum tuberosum) ortholog of SXD1 was isolated and functionally characterized. StSXD1 encoded a protein with high TC activity in vitro, and chloroplastic localization was demonstrated by transient expression of green fluorescent protein-tagged fusion constructs. RNAi-mediated silencing of StSXD1 in transgenic potato plants resulted in the disruption of TC activity and severe tocopherol deficiency similar to the orthologous sxd1 and vte1 mutants. The nearly complete absence of tocopherols caused a characteristic photoassimilate export-defective phenotype comparable to sxd1, which appeared to be a consequence of vascular-specific callose deposition observed in source leaves. CO2 assimilation rates and photosynthetic gene expression were decreased in source leaves in close correlation with excess sugar accumulation, suggesting a carbohydrate-mediated feedback inhibition rather than a direct impact of tocopherol deficiency on photosynthetic capacity. This conclusion is further supported by an increased photosynthetic capacity of young leaves regardless of decreased tocopherol levels. Our data provide evidence that tocopherol deficiency leads to impaired photoassimilate export from source leaves in both monocot and dicot plant species and suggest significant differences among C3 plants in response to tocopherol reduction.
机译:生育酚(维生素E)是亲脂性抗氧化剂,被认为在保护叶绿体膜和光合作用设备免受光氧化损害方面起着关键作用。在最近发现Suc出口缺陷型玉米(Zea mays)突变体(sxd1)携带生育酚环化酶(TC)缺陷并因此缺乏生育酚之后,提出了生育酚的其他非抗氧化功能。但是,相应的维生素E缺乏1拟南芥突变体(vte1)缺乏类似于sxd1的表型,表明C4和C3植物之间生育酚功能存在差异。因此,在这项研究中,分离了马铃薯SXD1的直系同源基因并对其功能进行了表征。 StSXD1在体外编码具有高TC活性的蛋白质,并且通过绿色荧光蛋白标记的融合构建体的瞬时表达证明了叶绿体定位。 RNAi介导的StSXD1在转基因马铃薯植株中的沉默导致TC活性的破坏和严重的生育酚缺乏症,类似于直系同源的sxd1和vte1突变体。几乎没有生育酚会导致与sxd1相媲美的特征性光同化出口缺陷型表型,这似乎是在源叶中观察到的血管特异性call质沉积的结果。与过量糖分积累密切相关的源叶中CO2同化率和光合基因表达下降,表明碳水化合物介导的反馈抑制作用而不是生育酚缺乏对光合能力的直接影响。无论生育酚水平降低如何,幼叶的光合作用能力增强都进一步支持了这一结论。我们的数据提供了证据,表明生育酚缺乏会导致单子叶植物和双子叶植物物种中源叶的光同化出口受损,并表明C3植物之间对生育酚减少的反应存在显着差异。

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