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Exploring Flowering Genes in Isabgol (Plantago ovataForsk.) Through Transcriptome Analysis

机译:通过转录组分析探索Isabgol(Plantago Ovataforsk的开花基因

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Background Flowering is one of the major developmental processes that govern the economic yield of crop plants. However, little is known about the molecular mechanisms underlying flowering in Isabgol, an important high-value medicinal crop. Here, we analyzed the leaf transcriptome of early and late flowering genotypes by high throughput next-generation sequencing to uncover the genes and pathways involved in flowering time and flower development. Results Illumina paired-end sequencing of Isabgol leaves at the stem elongation stage, generated 8,976,119 and 4,282,684 reads respectively in DPO-14 (early flowering) and DPO-185 (late flowering) genotypes. The sequence assembly resulted in 40,175 and 39,533 transcripts respectively in early and late genotypes. A total of 17,768 (95.50) in DPO-14 and 21,255 (94.10) in DPO-185 CDS were annotated. There were 8981CDS were differentially expressed of which 1220 (13.58%) were significantly upregulated while 1485 (16.53%) CDS were significantly downregulated in DPO-185 compared with DPO-14. In total, 229 genes were identified belongs to distinct flowering pathways in Isabgol. A putative schematic network of flowering pathway regulation in Isabgol was proposed. Significant DEGs (60 genes) related to flowering time and flower development were detected between the early and late flowering genotypes. Significant differences in fold change expression of 17 genes were observed in early and late flowering genotypes. Conclusion Many differentially expressed genes (DEGs) involved in flowering time and flower development were identified. The expression data will serve as a resource for unraveling the functions of specific genes involved in flower development in Isabgol and other plants. These findings are significant for further understanding of the molecular basis for flowering time regulation, breeding, and molecular biology in Isabgol as well as other crop plants.
机译:背景开花是决定作物经济产量的主要发育过程之一。然而,对于重要的高价值药用作物Isabgol开花的分子机制知之甚少。在这里,我们通过高通量下一代测序分析了早花和晚花基因型的叶转录组,以揭示与开花时间和花发育有关的基因和途径。结果Illumina在茎伸长期对Isabgol叶片进行配对末端测序,在DPO-14(早花)和DPO-185(晚花)基因型中分别产生8976119和4282684个读取。序列组装在早期和晚期基因型中分别产生40175和39533个转录本。在DPO-14和DPO-185光盘中,分别标注了17768张(95.50)和21255张(94.10)。与DPO-14相比,DPO-185中有8981CDS差异表达,其中1220(13.58%)CDS显著上调,1485(16.53%)CDS显著下调。共鉴定出229个基因属于Isabgol的不同开花途径。提出了Isabgol开花途径调控的一个假定的示意图网络。在早花和晚花基因型之间检测到与开花时间和花发育相关的显著DEGs(60个基因)。在开花早期和开花晚期基因型中,17个基因的折叠变化表达存在显著差异。结论发现了许多与开花时间和花发育有关的差异表达基因。表达数据将作为一种资源,用于揭示伊莎贝尔和其他植物花发育相关的特定基因的功能。这些发现对于进一步了解伊莎贝尔和其他作物开花时间调节、育种和分子生物学的分子基础具有重要意义。

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