Zhao Hansheng, Lou Yongfeng, Sun Huayu, Li Lichao, Wang Lili, Dong Lili, Gao Zhimin
State Forestry Administration Key Open Laboratory on the Science and Technology of Bamboo and Rattan, Beijing, 100102, China.
Institute of Gene Science for Bamboo and Rattan Resources, International Center for Bamboo and Rattan, Beijing, 100102, China.
BMC Plant Biol. 2016 Jan 28;16:34. doi: 10.1186/s12870-016-0720-9.
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.
光合作用作为植物新陈代谢的能量来源起着至关重要的作用,其效率可能会因非生物胁迫而大幅降低。毛竹(Phyllostachys edulis)是一种具有重要生态和经济价值的可再生且用途广泛的资源,在自然环境中会遭遇大幅度的高光胁迫。然而,竹子中响应高光的基因表达谱尚不明确。
我们首先对经高光(1200 μmol·m(-2)·s(-1))处理的毛竹叶片进行了生理实验。基于生理结果,分别选取高光处理0小时(CK)、0.5小时(0.5H)和8小时(8H)的三个叶片样本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以统计学显著值(FPKM≥1)表达,并且RNA-Seq数据通过定量实时PCR进行了验证。此外,检测到一些显著的基因表达变化。例如,在0.5H与CK比较中检测到154个差异表达基因,8H与CK比较中有710个,在0.5H与8H比较中也鉴定出429个差异表达基因。此外,细化了47个与光合作用密切相关的基因注释,包括35个注释为捕光叶绿素a/b结合(LHC)蛋白的基因、9个LHC样蛋白和3个PsbS。此外,进一步分析了光合作用中活性氧(ROS)的途径。共鉴定出171个与ROS清除相关的基因。一些上调的转录因子,如NAC、WRKY、AR2/ERF和bHLH,主要集中在短期响应中,而C2H2、HSF、bZIP和MYB在对高光的短期和中期响应中大量参与。
基于毛竹对高光响应的基因表达分析,我们从而确定了全局基因表达模式,细化了LHC蛋白、LHC样蛋白和PsbS的注释,检测了ROS途径,并鉴定了参与光合及相关代谢调控的ROS清除基因和转录因子。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。