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Disruption of essential plastid gene expression caused by T7 RNA polymerase-mediated transcription of plastid transgenes during early seedling development

机译:T7 RNA聚合酶介导的质体转基因在幼苗早期发育过程中引起的基本质体基因表达的破坏

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Transcription of plastid transgenes by plastid-targeted T7 RNA polymerase (ptT7RNAP) during early seedling development in tobacco was associated with a pale-green leaf phenotype, depletion of plastid rRNAs and arrest of shoot development. Extensive analysis of mutant seedlings at the transcript level using DNA microarrays and RNA gel blotting revealed severe disruption of plastid rRNA accumulation at 4-days post-germination and reduced transcript accumulation for the essential gene clpP. Several nuclear genes encoding plastid proteins were differentially regulated in mutant seedlings over time. Ef-Tu was upregulated at 4-days post-germination and then subsequently downregulated, while RbcS was already downregulated at this early time point. The downregulation of nuclear genes encoding plastid proteins suggests disruption of plastid-to-nucleus signalling. In contrast, transcripts of three plastid genes showed increased accumulation in mutant seedlings. Transcripts of ndhC and ndhK accumulated at high levels possibly due to T7RNAP-mediated enhancement of transcription, while ptT7RNAP-mediated transcription through the phage T7 Tφ terminator into the adjacent plastome increased the level of accD transcripts. The leakiness of the Tφ terminator has implications for the use of T7RNAP-based expression systems in plastid biotechnology.
机译:在烟草幼苗早期发育过程中,质体靶向的T7 RNA聚合酶(ptT7RNAP)对质体转基因的转录与淡绿色的叶片表型,质体rRNA的耗竭和芽发育的停止有关。使用DNA微阵列和RNA凝胶印迹在转录水平上对突变苗进行了广泛的分析,发现发芽后4天,质体rRNA积累受到严重破坏,基本基因clpP的转录积累减少。随着时间的推移,突变体幼苗中的几个编码质体蛋白的核基因受到了不同的调控。 Ef-Tu在发芽后4天被上调,然后被下调,而RbcS在这个早期时间点已经被下调。编码质体蛋白的核基因的下调表明质体到核信号的破坏。相反,三个质体基因的转录本在突变苗中显示出增加的积累。 ndhC和ndhK的转录本高水平积累,可能是由于T7RNAP介导的转录增强,而ptT7RNAP介导的通过噬菌体T7Tφ终止子进入邻近质体的转录增加了accD转录本的水平。 Tφ终止子的泄漏对在质体生物技术中使用基于T7RNAP的表达系统有影响。

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