4.7 Article

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

期刊

BMC PLANT BIOLOGY
卷 16, 期 -, 页码 -

出版社

BMC
DOI: 10.1186/s12870-016-0720-9

关键词

Moso bamboo; RNA-Seq; Photosynthesis; Gene expression; Transcript factors

资金

  1. Sub-Project of National Science and Technology Support Plan of the Twelfth Five-Year in China [2015BAD04B03, 2015BAD04B01]
  2. Fundamental Research Funds for International Center for Bamboo and Rattan [1632015008]
  3. National Science Foundation of China [31400557, 31370588]

向作者/读者索取更多资源

Background: 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. Results: We firstly performed physiological experiments on moso bamboo leaves treated with high light (1200 mu mol.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. Conclusion: 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.

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