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Tracking Difference in Gene Expression in a Time-Course Experiment Using Gene Set Enrichment Analysis
Authors:Pui Shan Wong  Michihiro Tanaka  Yoshihiko Sunaga  Masayoshi Tanaka  Takeaki Taniguchi  Tomoko Yoshino  Tsuyoshi Tanaka  Wataru Fujibuchi  Sachiyo Aburatani
Institution:1. CBRC, National Institute of AIST, Tokyo, Japan.; 2. Center for iPS Research and Application, Kyoto University, Kyoto, Japan.; 3. Institute of Engineering, Tokyo University of Agriculture and Technology, Tokyo, Japan.; 4. JST, CREST, Sanbancho 5, Chiyoda-ku, Tokyo, Japan.; 5. Mitsubishi Research Institute, Inc., Tokyo, Japan.; University of North Carolina at Charlotte, United States of America,
Abstract:Fistulifera sp. strain JPCC DA0580 is a newly sequenced pennate diatom that is capable of simultaneously growing and accumulating lipids. This is a unique trait, not found in other related microalgae so far. It is able to accumulate between 40 to 60% of its cell weight in lipids, making it a strong candidate for the production of biofuel. To investigate this characteristic, we used RNA-Seq data gathered at four different times while Fistulifera sp. strain JPCC DA0580 was grown in oil accumulating and non-oil accumulating conditions. We then adapted gene set enrichment analysis (GSEA) to investigate the relationship between the difference in gene expression of 7,822 genes and metabolic functions in our data. We utilized information in the KEGG pathway database to create the gene sets and changed GSEA to use re-sampling so that data from the different time points could be included in the analysis. Our GSEA method identified photosynthesis, lipid synthesis and amino acid synthesis related pathways as processes that play a significant role in oil production and growth in Fistulifera sp. strain JPCC DA0580. In addition to GSEA, we visualized the results by creating a network of compounds and reactions, and plotted the expression data on top of the network. This made existing graph algorithms available to us which we then used to calculate a path that metabolizes glucose into triacylglycerol (TAG) in the smallest number of steps. By visualizing the data this way, we observed a separate up-regulation of genes at different times instead of a concerted response. We also identified two metabolic paths that used less reactions than the one shown in KEGG and showed that the reactions were up-regulated during the experiment. The combination of analysis and visualization methods successfully analyzed time-course data, identified important metabolic pathways and provided new hypotheses for further research.
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