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Differential Expression Profiling of Microspores During the Early Stages of Isolated Microspore Culture Using the Responsive Barley Cultivar Gobernadora

机译:使用响应性大麦品种Gobernadora分离小孢子培养早期的小孢子差异表达谱

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摘要

In barley, it is possible to induce embryogenesis in the haploid and uninucleate microspore to obtain a diploid plant that is perfectly homozygous. To change developmental fates in this fashion, microspores need to engage in cellular de-differentiation, interrupting the pollen formation, and restore totipotency prior to engaging in embryogenesis. In this work, we used the barley cultivar Gobernadora to characterize the transcriptome of microspores prior to (day 0) and immediately after (days 2 and 5) the application of a stress pretreatment. A deep RNA-seq analysis revealed that microspores at these three time points exhibit a transcriptome of ∼14k genes, ∼90% of which were shared. An expression analysis identified a total of 3,382 differentially expressed genes (DEGs); of these, 2,155 and 2,281 DEGs were respectively identified when contrasting expression at days 0 and 2 and at days 2 and 5. These define 8 expression profiles in which DEGs share a common up- or down-regulation at these time points. Up-regulation of numerous glutathione S-transferase and heat shock protein genes as well as down-regulation of ribosomal subunit protein genes was observed between days 0 and 2. The transition from microspores to developing embryos (days 2 vs. 5) was marked by the induction of transcription factor genes known to play important roles in early embryogenesis, numerous genes involved in hormone biosynthesis and plant hormonal signal transduction in addition to genes involved in secondary metabolism. This work sheds light on transcriptional changes accompanying an important developmental shift and provides candidate biomarkers for embryogenesis in barley.
机译:在大麦中,有可能在单倍体和单核小孢子中诱导胚胎发生,从而获得完全纯合的二倍体植物。为了以这种方式改变发育命运,小孢子需要进行细胞去分化,中断花粉形成并恢复全能,然后再进行胚胎发生。在这项工作中,我们使用大麦栽培品种Gobernadora表征了施加压力预处理之前(第0天)和之后(第2天和第5天)的小孢子转录组。深入的RNA-seq分析显示,在这三个时间点的小孢子表现出约14k个基因的转录组,其中约90%的基因被共享。表达分析鉴定出总共3,382个差​​异表达基因(DEG)。其中,分别在第0天和第2天以及第2天和第5天对比表达时,分别鉴定了2155个和2281个DEG。它们定义了8个表达谱,其中DEG在这些时间点共有共同的上调或下调。在第0天和第2天之间观察到许多谷胱甘肽S-转移酶和热休克蛋白基因的上调以及核糖体亚基蛋白基因的下调。从小孢子到发育中的胚胎的过渡(第2天比第5天)的标记为已知在早期胚胎发生中起重要作用的转录因子基因的诱导,除参与次级代谢的基因外,还参与激素生物合成和植物激素信号转导的众多基因。这项工作揭示了伴随重要发育变化的转录变化,并为大麦的胚胎发生提供了候选生物标记。

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