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Suppressing Farnesyl Diphosphate Synthase Alters Chloroplast Development and Triggers Sterol-Dependent Induction of Jasmonate- and Fe-Related Responses

机译:抑制法呢基二磷酸合酶改变叶绿体的发展并触发茉莉酸酯和铁相关反应的甾醇依赖诱导。

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摘要

Farnesyl diphosphate synthase (FPS) catalyzes the synthesis of farnesyl diphosphate from isopentenyl diphosphate and dimethylallyl diphosphate. Arabidopsis (Arabidopsis thaliana) contains two genes (FPS1 and FPS2) encoding FPS. Single fps1 and fps2 knockout mutants are phenotypically indistinguishable from wild-type plants, while fps1/fps2 double mutants are embryo lethal. To assess the effect of FPS down-regulation at postembryonic developmental stages, we generated Arabidopsis conditional knockdown mutants expressing artificial microRNAs devised to simultaneously silence both FPS genes. Induction of silencing from germination rapidly caused chlorosis and a strong developmental phenotype that led to seedling lethality. However, silencing of FPS after seed germination resulted in a slight developmental delay only, although leaves and cotyledons continued to show chlorosis and altered chloroplasts. Metabolomic analyses also revealed drastic changes in the profile of sterols, ubiquinones, and plastidial isoprenoids. RNA sequencing and reverse transcription-quantitative polymerase chain reaction transcriptomic analysis showed that a reduction in FPS activity levels triggers the misregulation of genes involved in biotic and abiotic stress responses, the most prominent one being the rapid induction of a set of genes related to the jasmonic acid pathway. Down-regulation of FPS also triggered an iron-deficiency transcriptional response that is consistent with the iron-deficient phenotype observed in FPS-silenced plants. The specific inhibition of the sterol biosynthesis pathway by chemical and genetic blockage mimicked these transcriptional responses, indicating that sterol depletion is the primary cause of the observed alterations. Our results highlight the importance of sterol homeostasis for normal chloroplast development and function and reveal important clues about how isoprenoid and sterol metabolism is integrated within plant physiology and development.
机译:法呢基二磷酸合酶(FPS)催化由异戊烯基二磷酸和二甲基烯丙基二磷酸合成法呢基二磷酸。拟南芥(Arabidopsis thaliana)包含两个编码FPS的基因(FPS1和FPS2)。从表型上看,单个fps1和fps2敲除突变体与野生型植物在表型上没有区别,而fps1 / fps2双重突变体则对胚胎致死。为了评估FPS下调在胚胎后发育阶段的影响,我们生成了拟南芥条件表达突变体,该突变体表达了被设计为同时沉默两个FPS基因的人工microRNA。萌发引起的沉默诱导迅速引起萎黄病和强烈的发育表型,导致幼苗死亡。然而,尽管叶片和子叶继续显示出萎黄病和叶绿体改变,但种子发芽后FPS沉默只会导致轻微的发育延迟。代谢组学分析还显示,固醇,泛醌和质体类异戊二烯的概况发生了巨大变化。 RNA测序和逆转录定量聚合酶链反应转录组分析表明,FPS活性水平降低会触发涉及生物和非生物胁迫反应的基因的调控异常,最突出的一个是迅速诱导了与茉莉花相关的一组基因酸途径。 FPS的下调也触发了铁缺乏的转录反应,这与在FPS沉默的植物中观察到的铁缺乏的表型一致。通过化学和遗传阻滞对固醇生物合成途径的特异性抑制模仿了这些转录反应,表明固醇耗竭是观察到的改变的主要原因。我们的结果突出了固醇稳态对于正常叶绿体发育和功能的重要性,并揭示了关于类异戊二烯和固醇代谢如何在植物生理和发育中整合的重要线索。

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