Comparative transcriptomics method to infer gene coexpression networks and its applications to maize and rice leaf transcriptomes

• Published in: Proceedings of the National Academy of Sciences - PNAS Vol. 116; no. 8; pp. 3091 - 3099
• Main Authors: Chang, Yao-Ming, Lin, Hsin-Hung, Liu, Wen-Yu, Yu, Chun-Ping, Chen, Hsiang-June, Wartini, Putu Puja, Kao, Yi-Ying, Wu, Yeh-Hua, Lin, Jinn-Jy, Lu, Mei-Yeh Jade, Tu, Shih-Long, Wu, Shu-Hsing, Shiu, Shin-Han, Ku, Maurice S. B., Li, Wen-Hsiung
• Format: Journal Article
• Language: English
• Published: United States National Academy of Sciences 19-02-2019
• Series: PNAS Plus
• Subjects: Anatomy; Biological activity; Biological Sciences; Corn; Darkness; Gene expression; Gene Expression Regulation, Plant - genetics; Gene Regulatory Networks - genetics; Genes; Leaves; Networks; Oryza; Oryza - genetics; Photoperiod; Photosynthesis; Photosynthesis - genetics; Plant Leaves - genetics; Plant Proteins; PNAS Plus; Regulators; Ribulose-bisphosphate carboxylase; Ribulose-Bisphosphate Carboxylase - genetics; Time series; Transcriptome - genetics; Zea mays; Zea mays - genetics; gene coexpression; C4 enzymes; comparative transcriptomics; Kranz anatomy
• ISSN: 0027-8424; 1091-6490
• DOI: 10.1073/pnas.1817621116

Time-series transcriptomes of a biological process obtained under different conditions are useful for identifying the regulators of the process and their regulatory networks. However, such data are 3D (gene expression, time, and condition), and there is currently no method that can deal with their full complexity. Here, we developed a method that avoids time-point alignment and normalization between conditions. We applied it to analyze time-series transcriptomes of developing maize leaves under light–dark cycles and under total darkness and obtained eight time-ordered gene coexpression networks (TO-GCNs), which can be used to predict upstream regulators of any genes in the GCNs. One of the eight TO-GCNs is light-independent and likely includes all genes involved in the development of Kranz anatomy, which is a structure crucial for the high efficiency of photosynthesis in C₄ plants. Using this TO-GCN, we predicted and experimentally validated a regulatory cascade upstream of SHORTROOT1, a key Kranz anatomy regulator. Moreover, we applied the method to compare transcriptomes from maize and rice leaf segments and identified regulators of maize C₄ enzyme genes and RUBISCO SMALL SUBUNIT2. Our study provides not only a powerful method but also novel insights into the regulatory networks underlying Kranz anatomy development and C₄ photosynthesis.