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Nuclear SDH2-1 and SDH2-2 Genes Encoding the Iron-Sulfur Subunit of Mitochondrial Complex II in Arabidopsis Have Distinct Cell-Specific Expression Patterns and Promoter Activities

机译:拟南芥中编码线粒体复合体II铁硫亚基的核SDH2-1和SDH2-2基因具有不同的细胞特异性表达模式和启动子活性

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摘要

Three different nuclear genes encode the essential iron-sulfur subunit of mitochondrial complex II (succinate dehydrogenase) in Arabidopsis (Arabidopsis thaliana), raising interesting questions about their origin and function. To find clues about their role, we have undertaken a detailed analysis of their expression. Two genes (SDH2-1 and SDH2-2) that likely arose via a relatively recent duplication event are expressed in all organs from adult plants, whereas transcripts from the third gene (SDH2-3) were not detected. The tissue- and cell-specific expression of SDH2-1 and SDH2-2 was investigated by in situ hybridization. In flowers, both genes are regulated in a similar way. Enhanced expression was observed in floral meristems and sex organ primordia at early stages of development. As flowers develop, SDH2-1 and SDH2-2 transcripts accumulate in anthers, particularly in the tapetum, pollen mother cells, and microspores, in agreement with an essential role of mitochondria during anther development. Interestingly, in contrast to the situation in flowers, only SDH2-2 appears to be expressed at a significant level in root tips. Strong labeling was observed in all cell layers of the root meristematic zone, and a cell-specific pattern of expression was found with increasing distance from the root tip, as cells attain their differentiated state. Analysis of transgenic Arabidopsis plants carrying SDH2-1 and SDH2-2 promoters fused to the β-glucuronidase reporter gene indicate that both promoters have similar activities in flowers, driving enhanced expression in anthers and/or pollen, and that only the SDH2-2 promoter is active in root tips. These β-glucuronidase staining patterns parallel those obtained by in situ hybridization, suggesting transcriptional regulation of these genes. Progressive deletions of the promoters identified regions important for SDH2-1 expression in anthers and/or pollen and for SDH2-2 expression in anthers and/or pollen and root tips. Interestingly, regions driving enhanced expression in anthers are differently located in the two promoters.
机译:三个不同的核基因编码拟南芥(Arabidopsis thaliana)中线粒体复合体II(琥珀酸脱氢酶)的必需铁硫亚基,引发了有关其起源和功能的有趣问题。为了找到有关它们作用的线索,我们对其表达进行了详细分析。在成年植物的所有器官中都表达了可能通过相对较新的复制事件产生的两个基因(SDH2-1和SDH2-2),而未检测到第三个基因(SDH2-3)的转录本。通过原位杂交研究了SDH2-1和SDH2-2的组织和细胞特异性表达。在花朵中,两个基因的调控方式相似。在发育的早期,在花分生组织和性器官原基中观察到表达增强。随着花的发育,SDH2-1和SDH2-2转录物在花药中积累,特别是在绒毡层,花粉母细胞和小孢子中积累,这与线粒体在花药发育过程中的重要作用相一致。有趣的是,与花的情况相反,只有SDH2-2似乎在根尖中以高水平表达。在根分生组织区的所有细胞层中均观察到强标记,随着细胞达到其分化状态,随着距根尖距离的增加,发现了一种细胞特异性表达模式。对携带融合有β-葡萄糖醛酸糖苷酶报道基因SDH2-1和SDH2-2启动子的转基因拟南芥植物的分析表明,两个启动子在花中具有相似的活性,驱动花药和/或花粉的表达增强,并且仅SDH2-2启动子在根提示中很活跃。这些β-葡萄糖醛酸苷酶染色模式与通过原位杂交获得的染色模式平行,表明这些基因的转录调控。启动子的逐步缺失鉴定出对于花药和/或花粉中的SDH2-1表达和花药和/或花粉和根尖中的SDH2-2表达重要的区域。有趣的是,驱动花药中增强表达的区域位于两个启动子中的位置不同。

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