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激光微切割水涝玉米根改变表达的植物血朊蛋白亚区中转录本和生物过程的空间鉴定。

Spatial identification of transcripts and biological processes in laser micro-dissected sub-regions of waterlogged corn roots with altered expression of phytoglobin.

机构信息

Botany Department, Faculty of Science, Kafrelsheikh University, 33516, Kafr El-Sheikh, Egypt.

Department of Botany, Faculty of Science, Tanta University, Tanta, 31527, Gharbia, Egypt.

出版信息

Plant Physiol Biochem. 2019 Jun;139:350-365. doi: 10.1016/j.plaphy.2019.03.036. Epub 2019 Mar 27.

DOI:10.1016/j.plaphy.2019.03.036
PMID:30952087
Abstract

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.

摘要

过量表达玉米植物血球蛋白 ZmPgb1.2 增加了植物对淹水的耐受性,而抑制 ZmPgb1.2 则会损害植物的生长。为了解析 ZmPgb1.2 在缺氧条件下引起的特定隔室的转录变化,使用下一代 RNA 测序技术对 WT 和过表达 ZmPgb1.2 的 [ZmPgb1.2(S)] 植物的淹水根的激光微切割亚区进行了全局转录分析。这些亚区包括分生区、伸长区和成熟区的隔室。在 ZmPgb1.2 的上调表达中差异表达的 149 个基因中,有 78 个发生在分生区,包括参与茉莉酸合成和反应、抗坏血酸代谢和乙烯信号转导的基因。ZmPgb1.2 对这些基因的调控,在已知 Pgbs 功能的背景下进行了讨论,并通过监测其在抑制 ZmPgb1.2 的淹水根分生区细胞中的表达进行了进一步验证。在伸长区中,27 个因 ZmPgb1.2 过表达而差异表达的基因中,丙酮酸激酶和醇脱氢酶表现出与组织中 ZmPgb1.2 水平相关的表达模式。在过表达 ZmPgb1.2 的伸长区缺氧区域中这两种酶的转录诱导表明发酵途径的激活,这可能是维持代谢通量和产生 ATP 以支持细胞伸长所必需的。

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