Takahashi Sota, Okubo Riho, Kanesaki Yu, Zhou Baifeng, Takaya Kazuhiro, Watanabe Satoru, Tanaka Kan, Imamura Sousuke
Interdisciplinary Graduate School of Science and Engineering, Tokyo Institute of Technology, Yokohama 226-8503, Japan.
Laboratory for Chemistry and Life Science, Institute of Innovative Research, Tokyo Institute of Technology, Yokohama 226-8503, Japan.
Plants (Basel). 2021 May 13;10(5):971. doi: 10.3390/plants10050971.
Microalgal triacylglycerols (TAGs) are a good feedstock for liquid biofuel production. Improving the expression and/or function of transcription factors (TFs) involved in TAG accumulation may increase TAG content; however, information on microalgae is still lacking. In this study, 14 TFs in the unicellular red alga were identified as candidate TFs regulating TAG accumulation using available transcriptome and phosphoproteome data under conditions driving TAG accumulation. To investigate the roles of these TFs, we constructed TF-overexpression strains and analyzed lipid droplet (LD) formation and TAG contents in the cells grown under standard conditions. Based on the results, we identified four TFs involved in LD and TAG accumulation. RNA-Seq analyses were performed to identify genes regulated by the four TFs using each overexpression strain. Among the TAG biosynthesis-related genes, only the gene encoding the endoplasmic reticulum-localized lysophosphatidic acid acyltransferase 1 (LPAT1) was notably increased among the overexpression strains. In the LPAT1 overexpression strain, TAG accumulation was significantly increased compared with the control strain under normal growth conditions. These results indicate that the four TFs positively regulate TAG accumulation by changing their target gene expression in .
微藻三酰甘油(TAGs)是液体生物燃料生产的优质原料。提高参与TAG积累的转录因子(TFs)的表达和/或功能可能会增加TAG含量;然而,关于微藻的相关信息仍然匮乏。在本研究中,利用驱动TAG积累条件下的可用转录组和磷酸化蛋白质组数据,在单细胞红藻中鉴定出14个TFs作为调节TAG积累的候选TFs。为了研究这些TFs的作用,我们构建了TF过表达菌株,并分析了在标准条件下生长的细胞中脂滴(LD)的形成和TAG含量。基于这些结果,我们鉴定出4个参与LD和TAG积累的TFs。利用每个过表达菌株进行RNA测序分析,以鉴定受这4个TFs调控的基因。在TAG生物合成相关基因中,在过表达菌株中只有编码内质网定位的溶血磷脂酸酰基转移酶1(LPAT1)的基因显著增加。在正常生长条件下,与对照菌株相比,LPAT1过表达菌株中的TAG积累显著增加。这些结果表明,这4个TFs通过改变其在[具体藻类名称未给出]中的靶基因表达来正向调节TAG积累。