Chung Moon-Soo, Lee Sungbeom, Min Ji-Hee, Huang Ping, Ju Hyun-Woo, Kim Cheol Soo
Korea Atomic Energy Research Institute, Jeollabuk-do 580-185, South Korea; Department of Plant Biotechnology, Chonnam National University, Gwangju 500-757, South Korea.
Korea Atomic Energy Research Institute, Jeollabuk-do 580-185, South Korea.
Plant Physiol Biochem. 2016 Jul;104:155-64. doi: 10.1016/j.plaphy.2016.03.029. Epub 2016 Mar 23.
Biochemical, genetic, physiological, and molecular research in plants has demonstrated a central role of glucose (Glc) in the control of plant growth, metabolism, and development, and has revealed networks that integrate light, stresses, nutrients, and hormone signaling. Previous studies have reported that AtPGR protein as potential candidates for Glc signaling protein. In the present study, we characterized transcription factors that bind to the upstream region of the AtPGR gene isolated using the yeast one-hybrid screening with an Arabidopsis cDNA library. One of the selected genes (AtSTKL) appeared to confer elevated sensitivity to Glc response. Overexpression of AtSTKLs (AtSTKL1 and AtSTKL2) increased the sensitivity to Glc during the post-germination stages. In contrast, atstkl1 and atstkl2 antisense lines displayed reduced sensitivity to high Glc concentration during the early seedling stage. Furthermore, we showed that the two AtSTKLs bind to the 5'-GCCT-3' element of the upstream promoter region of the AtPGR gene in vitro and repress the beta-glucuronidase (GUS) activity in AtPGR promoter-GUS (P999-GUS) transgenic plants. Green fluorescent protein (GFP)-tagged AtSTKLs were localized in the nuclei of transgenic Arabidopsis cells. Collectively, these results suggest that AtSTKL1 and AtSTKL2 function both as repressors of AtPGR transcription and as novel transcription factors in the Glc signaling pathway.
植物中的生化、遗传、生理和分子研究表明,葡萄糖(Glc)在控制植物生长、代谢和发育中起核心作用,并揭示了整合光、胁迫、营养和激素信号的网络。先前的研究报道,AtPGR蛋白是Glc信号蛋白的潜在候选者。在本研究中,我们对通过酵母单杂交筛选与拟南芥cDNA文库分离出的AtPGR基因上游区域结合的转录因子进行了表征。其中一个选定的基因(AtSTKL)似乎赋予了对Glc反应更高的敏感性。AtSTKLs(AtSTKL1和AtSTKL2)的过表达在萌发后阶段增加了对Glc的敏感性。相反,atstkl1和atstkl2反义系在幼苗早期对高Glc浓度的敏感性降低。此外,我们表明这两个AtSTKLs在体外与AtPGR基因上游启动子区域的5'-GCCT-3'元件结合,并抑制AtPGR启动子-GUS(P999-GUS)转基因植物中的β-葡萄糖醛酸酶(GUS)活性。绿色荧光蛋白(GFP)标记的AtSTKLs定位于转基因拟南芥细胞的细胞核中。总的来说,这些结果表明AtSTKL1和AtSTKL2既作为AtPGR转录的抑制因子,又作为Glc信号通路中的新型转录因子发挥作用。