Biotechnology Research Institute, Chinese Academy of Agricultural Sciences, Beijing 100081, China.
State Key Laboratory of Plant Physiology and Biochemistry, College of Biological Sciences, China Agricultural University, Beijing 100193, China.
Int J Mol Sci. 2019 Jan 4;20(1):167. doi: 10.3390/ijms20010167.
High salinity severely restrains plant growth and results in decrease of crop yield in agricultural production. Thus, it is of great significance to discover the crucial regulators involved in plant salt resistance. Here, we report a novel mutant, , which displays enhanced salt tolerance and dwarf phenotype, by screening from ethyl methane sulfonate (EMS) mutagenized rice mutant library. Genetic analysis showed that was caused by a single recessive locus. Map-based cloning and allelic test revealed that the phenotypes of were due to the mutation of , encoding the alpha subunit of heterotrimeric G protein (G). A point mutation (G to A) was identified at the splicing site (GT-AG) of the first intron in , which gives rise to the generation of abnormal mRNA splicing forms. Furthermore, 332 differentially abundant proteins (DAPs) were identified by using an Isobaric Tags for Relative and Absolute Quantitation(iTRAQ)-based proteomic technique from seedlings of and Kitaake in response to salt treatment. Gene Ontology (GO) and KEGG pathway enrichment analysis revealed these proteins were mainly involved in regulation of the processes such as metabolic pathways, photosynthesis and reactive oxygen species (ROS) homeostasis. Under salt stress, displayed lower ROS accumulation than Kitaake, which is consistent with the higher enzyme activities involved in ROS scavenging. Taken together, we propose that RGA1 is one of the regulators in salt response partially through ROS scavenging, which might be helpful in elucidating salt tolerant mechanisms of heterotrimeric G protein in rice.
高盐度严重抑制植物生长,导致农业生产中作物产量下降。因此,发现参与植物耐盐性的关键调节因子具有重要意义。在这里,我们通过筛选乙磺酸乙酯(EMS)诱变的水稻突变体文库,报告了一个新的突变体 ,它表现出增强的耐盐性和矮化表型。遗传分析表明 是由一个单一的隐性基因座引起的。基于图谱的克隆和等位基因测试表明, 的表型是由于 ,编码异三聚体 G 蛋白(G)的α亚基的突变。在 ,第一个内含子的剪接位点(GT-AG)处发现了一个点突变(G 到 A),导致异常 mRNA 剪接形式的产生。此外,通过使用基于等重同位素标记相对和绝对定量(iTRAQ)的蛋白质组学技术,从 和 Kitaake 的幼苗中鉴定出 332 种差异丰度蛋白(DAPs)对盐处理的响应。GO 和 KEGG 通路富集分析显示,这些蛋白主要参与代谢途径、光合作用和活性氧(ROS)稳态等过程的调节。在盐胁迫下, 比 Kitaake 表现出较低的 ROS 积累,这与参与 ROS 清除的酶活性较高一致。综上所述,我们提出 RGA1 是盐响应的调节剂之一,部分通过 ROS 清除,这可能有助于阐明水稻异三聚体 G 蛋白的耐盐机制。