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首页> 外文期刊>Plant Cell Reports >Transcriptomic analysis of floral initiation in litchi (Litchi chinensis Sonn.) based on de novo RNA sequencing
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Transcriptomic analysis of floral initiation in litchi (Litchi chinensis Sonn.) based on de novo RNA sequencing

机译:基于从头RNA测序的荔枝(Litchi chinensis Sonn。)花序的转录组学分析

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Comparative transcriptome analysis of litchi ( Litchi chinensis Sonn.) buds at two developmental stages revealed multiple processes involving various phytohormones regulating floral initiation, and expression of numerous flowering-related genes. Floral initiation is a critical and complicated plant developmental process involving interactions of numerous endogenous and environmental factors, but little is known about the complex network regulating floral initiation in litchi (Litchi chinensis Sonn.). Illumina second-generation sequencing is an efficient method for obtaining massive transcriptional information resulting from phase changes in plant development. In this study, comparative transcriptomic analysis was performed with resting and emerging panicle stage buds, to gain further understanding of the molecular mechanisms involved in floral initiation in litchi. Abundance analysis identified 5,928 unigenes exhibiting at least twofold differences in expression between the two bud stages. Of these, 4,622 unigenes were up-regulated and 1,306 were down-regulated in panicle-emerging buds compared with resting buds. KEGG pathway enrichment analysis revealed that unigenes exhibiting differential expression were involved in the metabolism and signal transduction of various phytohormones. The expression levels of unigenes annotated as auxin, cytokinin, jasmonic acid, and salicylic acid biosynthesis were up-regulated, whereas those unigenes annotated as abscisic acid biosynthesis were down-regulated during floral initiation. In addition, 188 unigenes exhibiting sequence similarities to known flowering-related genes from other plants were differentially expressed during floral initiation. Thirteen genes were selected for confirmation of expression levels using quantitative-PCR. Our results provide abundant sequence resources for studying mechanisms underlying floral initiation in litchi and establish a platform for further studies of litchi and other evergreen fruit trees
机译:荔枝(Litchi chinensis Sonn。)芽在两个发育阶段的比较转录组分析显示,多个过程涉及调节植物花序的各种植物激素,并表达了许多开花相关基因。花序萌发是至关重要的且复杂的植物发育过程,涉及许多内源性和环境因素的相互作用,但对于荔枝(Litchi chinensis Sonn。)中调控花序萌发的复杂网络知之甚少。 Illumina第二代测序是一种有效的方法,可用于获取因植物发育中的相变而产生的大量转录信息。在这项研究中,对静止的和新兴的圆锥花序期芽进行了转录组分析,以进一步了解荔枝花序萌发的分子机制。丰度分析确定了5928个单基因,在两个芽期之间表现出至少两倍的表达差异。与静息芽相比,在穗出芽中,有4,622个单基因被上调,而1,306个被下调。 KEGG通路富集分析表明,表现出差异表达的单基因参与了各种植物激素的代谢和信号转导。被注为生长素,细胞分裂素,茉莉酸和水杨酸生物合成的单基因的表达水平上调,而被注为脱落酸生物合成的单基因的表达水平在花启动过程中被下调。另外,在花序萌发期间差异表达了188个与其他植物的已知开花相关基因具有序列相似性的单基因。使用定量PCR选择了十三种基因用于表达水平的确认。我们的结果提供了丰富的序列资源,用于研究荔枝花序启动的机制,并为进一步研究荔枝和其他常绿果树建立了平台

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