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首页> 外文期刊>Plant Physiology and Biochemistry >Spatial identification of transcripts and biological processes in laser micro-dissected sub-regions of waterlogged corn roots with altered expression of phytoglobin
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Spatial identification of transcripts and biological processes in laser micro-dissected sub-regions of waterlogged corn roots with altered expression of phytoglobin

机译:激光微分玉米根激光微沉积子区的转录物和生物过程的空间鉴定,具有改变植物植物的表达改变

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摘要

Over-expression of the corn phytoglobin ZmPgb1.2 increases tolerance to waterlogging, while suppression of ZmPgb1.2 compromises plant growth. To unravel compartment-specific transcriptional changes evoked by ZmPgb1.2 during hypoxia, laser micro-dissected sub-regions from waterlogged roots of WT and ZmPgb1.2 overexpressing [ZmPgb1.2(S)] plants were probed for global transcriptional analysis using next generation RNA sequencing. These sub-regions included compartments within the meristematic, elongation, and maturation zone. Of the 149 genes differentially expressed by the up-regulation of ZmPgb1.2, 78 occurred within the meristematic region and included genes involved in jasmonic acid synthesis and response, ascorbic acid metabolism, and ethylene signalling. The ZmPgb1.2 regulation of these genes, discussed in the context of known functions of Pgbs, was further validated by monitoring their expression in meristematic cells of waterlogged roots suppressing ZmPgb1.2. Of the 27 genes differentially expressed by the over-expression of ZmPgb1.2 in the elongation zone, pyruvate kinase and alcohol dehydrogenase showed an expression pattern correlated to the level of ZmPgb1.2 in the tissue. The transcriptional induction of these two enzymes in hypoxic domains of the elongation zone over-expressing ZmPgb1.2 suggests the activation of the fermentation pathway which might be required to sustain metabolic flux and production of ATP in support of cell elongation.
机译:玉米植物植物ZMPGB1.2的过表达增加了对涝盐的耐受性,同时抑制ZMPGB1.2损害了植物生长。在缺氧期间,ZMPGB1.2引起的Unrapl盒特异性转录变化,来自WT和ZMPGB1.2的WTT和ZMPGB1.2的激光微沉积的亚区过表达的[ZMPGB1.2]植物,用于使用下一代进行全局转录分析RNA测序。这些子区域包括共同,伸长率和成熟区内的隔室。在通过ZMPGB1.2,78的上调差异表达的149个基因中,在注释中发生,包括参与Jasmonic酸合成和响应,抗坏血酸代谢和乙烯信号传导的基因。通过监测抑制ZMPGB1.2的浇水根部的共用细胞中,进一步验证了在PGB的已知功能的上下文中讨论这些基因的ZMPGB1.2调节。通过在伸长区中的ZMPGB1.2的过表达差异表达的27个基因,丙酮酸激酶和醇脱氢酶显示出与组织中ZMPGB1.2的水平相关的表达模式。在表达ZMPGB1.2的伸长区缺氧结构域中的这两种酶的转录诱导表明,发酵途径的激活,这可能需要维持代谢通量和ATP的载体的载体伸长率。

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