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Transcriptome and comparative gene expression analysis of Phyllostachys edulis in response to high light

机译:毛竹对强光的转录组和比较基因表达分析

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Photosynthesis plays a vital role as an energy source for plant metabolism, and its efficiency may be drastically reduced owing to abiotic stresses. Moso bamboo (Phyllostachys edulis), is a renewable and versatile resource with significant ecological and economic value, which encounters high light stress with large amplitude in natural environment. However, the gene expression profiles in response to high light were elusive in bamboo. We firstly performed physiological experiments on moso bamboo leaves treated with high light (1200?μmol?·?m?2?·?s?1). Based on the physiological results, three samples of leaves treated with high light for 0?h (CK), 0.5?h (0.5H), and 8?h (8H) were selected to perform further high-throughput RNA sequencing (RNA-Seq), respectively. Then, the transcriptomic result demonstrated that the most genes were expressed at a statistically significant value (FPKM?≥?1) and the RNA-Seq data were validated via quantitative real time PCR. Moreover, some significant gene expression changes were detected. For instance, 154 differentially expressed genes were detected in 0.5H vs. CK, those in 8H vs. CK were 710, and 429 differentially expressed genes were also identified in 0.5H vs.8?H. Besides, 47 gene annotations closely related to photosynthesis were refined, including 35 genes annotated as light-harvesting chlorophyll a/b-binding (LHC) proteins, 9 LHC-like proteins and 3 PsbSs. Furthermore, the pathway of reactive oxygen species (ROS) in photosynthesis was further analyzed. A total of 171 genes associated with ROS-scavenging were identified. Some up-regulated transcript factors, such as NAC, WRKY, AR2/ERF, and bHLH, mainly concentrated in short-term response, while C2H2, HSF, bZIP, and MYB were largely involved in short and middle terms response to high light. Based on the gene expression analysis of moso bamboo in response to high light, we thus identified the global gene expression patterns, refined the annotations of LHC protein, LHC-like protein and PsbS, detected the pathway of ROS as well as identified ROS-scavenging genes and transcription factors in the regulation of photosynthetic and related metabolisms. These findings maybe provide a starting point to interpret the molecular mechanism of photosynthesis in moso bamboo under high light stress.
机译:光合作用作为植物新陈代谢的能源起着至关重要的作用,由于非生物胁迫,光合作用的效率可能会大大降低。毛竹(Phyllostachys edulis)是一种可再生且用途广泛的资源,具有重要的生态和经济价值,在自然环境中遇到高强度的光胁迫。然而,在高光下,基因表达谱在竹中是难以捉摸的。我们首先在高光(1200?μmol?·?m?2?·?s?1)处理的毛竹叶上进行了生理实验。根据生理结果,选择了三个分别用高光处理0?h(CK),0.5?h(0.5H)和8?h(8H)的叶子样品,以进行进一步的高通量RNA测序(RNA- Seq)。然后,转录组结果表明,大多数基因表达具有统计学意义(FPKM≥1),并且通过定量实时PCR验证了RNA-Seq数据。此外,检测到一些显着的基因表达变化。例如,在0.5H vs. CK中检测到154个差异表达基因,在8H vs. CK中检测到710个,在0.5H vs.8?H中也鉴定出429个差异表达的基因。此外,完善了与光合作用密切相关的47个基因注释,包括35个被标记为光收集叶绿素a / b结合(LHC)的基因,9个LHC样蛋白和3个PsbSs。此外,进一步分析了光合作用中活性氧(ROS)的途径。总共鉴定了171个与ROS清除相关的基因。 NAC,WRKY,AR2 / ERF和bHLH等一些上调的转录因子主要集中在短期反应中,而C2H2,HSF,bZIP和MYB则主要参与短期和中期对强光的反应。通过对毛竹对强光的基因表达分析,我们确定了整体基因表达模式,完善了LHC蛋白,LHC样蛋白和PsbS的注释,检测了ROS的途径并鉴定了ROS清除基因和转录因子调控光合作用和相关代谢。这些发现可能为解释高光胁迫下毛竹光合作用的分子机制提供一个起点。

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