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Analysis of Differentially Expressed Genes in Tissues of Camellia sinensis during Dedifferentiation and Root Redifferentiation

机译:茶树去分化和根再分化过程中差异表达基因的分析

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摘要

Tissue culture is very important for identifying the gene function of Camellia sinensis (L.) and exploiting novel germplasm through transgenic technology. Regeneration system of tea plant has been explored but not been well established since the molecular mechanism of tea plant regeneration is not clear yet. In this study, transcriptomic analysis was performed in the initial explants of tea plant and their dedifferentiated and redifferentiated tissues. A total of 93,607 unigenes were obtained through de novo assembly, and 7,193 differentially expressed genes (DEGs) were screened out from the 42,417 annotated unigenes. Much more DEGs were observed during phase transition rather than at growth stages of callus. Our KOG and KEGG analysis, and qPCR results confirmed that phase transition of tea plant was closely related to the mechanism that regulate expression of genes encoding the auxin- and cytokinin-responsive proteins, transcription factor MYB15 and ethylene-responsive transcription factor ERF RAP2-12. These findings provide a reliable foundation for elucidating the mechanism of the phase transition and may help to optimize the regeneration system by regulating the gene expression pattern.
机译:组织培养对于鉴定茶树的基因功能和通过转基因技术开发新型种质非常重要。由于茶树再生的分子机制尚不清楚,因此已经探索了茶树再生系统,但尚未建立完善的体系。在这项研究中,在茶树的原始外植体及其去分化和再分化的组织中进行了转录组学分析。通过从头组装获得了总计93,607个单基因,并从42,417个带注释的单基因中筛选出7,193个差异表达基因(DEG)。在相变期间而不是在愈伤组织的生长阶段观察到更多的DEG。我们的KOG和KEGG分析以及qPCR结果证实,茶树的相变与调节生长素和细胞分裂素应答蛋白,转录因子MYB15和乙烯应答转录因子ERF RAP2-12的基因表达的调节机制密切相关。 。这些发现为阐明相变的机理提供了可靠的基础,并可能通过调节基因表达模式来帮助优化再生系统。

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