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首页> 外文期刊>Frontiers in Plant Science >De novo Sequencing of the Leaf Transcriptome Reveals Complex Light-Responsive Regulatory Networks in Camellia sinensis cv. Baijiguan
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De novo Sequencing of the Leaf Transcriptome Reveals Complex Light-Responsive Regulatory Networks in Camellia sinensis cv. Baijiguan

机译:叶片转录组的从头测序揭示了 Camellia sinensis cv中复杂的光响应调控网络。 百济关

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Tea plants ( Camellia sinensis L.) possess high genetic diversity that is important for breeding. One cultivar, Baijiguan , exhibits a yellow leaf phenotype, reduced chlorophyll (Chl) content, and aberrant chloroplast structures under high light intensity. In contrast, under low light intensity, the flush shoot from Baijiguan becomes green, the Chl content increases significantly, and the chloroplasts exhibit normal structures. To understand the underlying molecular mechanisms for these observations, we performed de novo transcriptome sequencing and digital gene expression (DGE) profiling using Illumina sequencing technology. De novo transcriptome assembly identified 88,788 unigenes, including 1652 transcription factors from 25 families. In total, 1993 and 2576 differentially expressed genes (DEGs) were identified in Baijiguan plants treated with 3 and 6 days of shade, respectively. Gene Ontology (GO) and pathway enrichment analyses indicated that the DEGs are predominantly involved in the ROS scavenging system, chloroplast development, photosynthetic pigment synthesis, secondary metabolism, and circadian systems. The light-responsive gene POR (protochlorophyllide oxidoreductase) and transcription factor HY5 were identified. Quantitative real-time PCR (qRT-PCR) analysis of 20 selected DEGs confirmed the RNA-sequencing (RNA-Seq) results. Overall, these findings suggest that high light intensity inhibits the expression of photosystem II 10-kDa protein ( PsbR ) in Baijiguan , thus affecting PSII stability, chloroplast development and chlorophyll biosynthesis.
机译:茶树(茶树)具有很高的遗传多样性,对育种很重要。在高光强度下,一个品种百济关表现出黄叶表型,叶绿素(Chl)含量降低,叶绿体结构异常。相反,在低光照条件下,百济关的嫩枝变为绿色,Chl含量显着增加,叶绿体呈现正常结构。为了了解这些观察的潜在分子机制,我们使用Illumina测序技术进行了从头转录组测序和数字基因表达(DGE)分析。从头转录组大会确定了88,788个单基因,包括来自25个家族的1652个转录因子。总共,在经过3天和6天遮荫处理的百济关植物中,分别鉴定出1993年和2576个差异表达基因(DEG)。基因本体论(GO)和途径富集分析表明,DEG主要参与ROS清除系统,叶绿体发育,光合色素合成,次级代谢和昼夜节律系统。鉴定出光响应基因POR(原叶绿素酰氧化还原酶)和转录因子HY5。实时定量PCR(qRT-PCR)对20个所选DEG的分析证实了RNA测序(RNA-Seq)的结果。总体而言,这些发现表明高光照强度会抑制白鸡关中Photosystem II 10-kDa蛋白(PsbR)的表达,从而影响PSII的稳定性,叶绿体的发育和叶绿素的生物合成。

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