Xu Lei, Zhao Hongyu, Ruan Wenyuan, Deng Minjuan, Wang Fang, Peng Jinrong, Luo Jie, Chen Zhixiang, Yi Keke
College of Life Sciences, Zhejiang University, Hangzhou 310058, China.
Key Laboratory of Plant Nutrition and Fertilizers, Ministry of Agriculture, Institute of Agricultural Resources and Regional Planning, Chinese Academy of Agricultural Sciences, Beijing 10081, China.
Plant Cell. 2017 Mar;29(3):560-574. doi: 10.1105/tpc.16.00665. Epub 2017 Mar 14.
Root meristem activity determines root growth and root architecture and consequently affects water and nutrient uptake in plants. However, our knowledge about the regulation of root meristem activity in crop plants is very limited. Here, we report the isolation and characterization of a short root mutant in rice () with reduced root meristem activity. This root growth defect is caused by a mutation in (), which encodes a 3-hydroxyacyl-CoA dehydrogenase, an enzyme involved in β-oxidation. The reduced root meristem activity of results from reduced salicylic acid (SA) levels and can be rescued by SA application. Furthermore, reduced SA levels are associated with reduced levels of reactive oxygen species (ROS) in , likely due to increased expression of redox and ROS-scavenging-related genes, whose increased expression is (at least in part) caused by reduced expression of the SA-inducible transcriptional repressors WRKY62 and WRKY76. Like SA, ROS application substantially increased root length and root meristem activity in These results suggest that AIM1 is required for root growth in rice due to its critical role in SA biosynthesis: SA maintains root meristem activity through promoting ROS accumulation by inducing the activity of WRKY transcriptional repressors, which repress the expression of redox and ROS-scavenging genes.
根分生组织活性决定根的生长和根系结构,进而影响植物对水分和养分的吸收。然而,我们对作物根分生组织活性调控的了解非常有限。在此,我们报道了水稻中一个根分生组织活性降低的短根突变体的分离和鉴定。这种根生长缺陷是由OsAIM1基因突变引起的,该基因编码一种3-羟酰基辅酶A脱氢酶,是参与β-氧化的一种酶。OsAIM1根分生组织活性降低是由于水杨酸(SA)水平降低所致,外源施加SA可使其恢复。此外,SA水平降低与OsAIM1中活性氧(ROS)水平降低有关,这可能是由于氧化还原和ROS清除相关基因的表达增加,而这些基因表达增加(至少部分)是由SA诱导的转录抑制因子WRKY62和WRKY76表达降低引起的。与SA一样,施加ROS显著增加了OsAIM1的根长和根分生组织活性。这些结果表明,由于OsAIM1在SA生物合成中的关键作用,它是水稻根生长所必需的:SA通过诱导WRKY转录抑制因子的活性促进ROS积累,从而维持根分生组织活性,而WRKY转录抑制因子可抑制氧化还原和ROS清除基因的表达。