Chen Wei, Tang Liqun, Li Qianlong, Cai Yicong, Ahmad Shakeel, Wang Yakun, Tang Shengjia, Guo Naihui, Wei Xiangjin, Tang Shaoqing, Shao Gaoneng, Jiao Guiai, Xie Lihong, Hu Shikai, Sheng Zhonghua, Hu Peisong
State Key Laboratory of Rice Biology/Key Laboratory of Rice Biology and Breeding, Ministry of Agriculture/China National Rice improvement Centre, National Rice Research Institute, Hangzhou, 310006, P. R. China.
Jiangxi Super-Rice Research and Development Center, Jiangxi Academy of Agricultural Sciences, National Engineering Center for Rice, Nanchang, P. R. China.
Rice (N Y). 2024 Jan 17;17(1):8. doi: 10.1186/s12284-024-00687-y.
As the source of isoprenoid precursors, the plastidial methylerythritol phosphate (MEP) pathway plays an essential role in plant development. Here, we report a novel rice (Oryza sativa L.) mutant ygl3 (yellow-green leaf3) that exhibits yellow-green leaves and lower photosynthetic efficiency compared to the wild type due to abnormal chloroplast ultrastructure and reduced chlorophyll content. Map-based cloning showed that YGL3, one of the major genes involved in the MEP pathway, encodes 4-hydroxy-3-methylbut-2-enyl diphosphate reductase, which is localized in the thylakoid membrane. A single base substitution in ygl3 plants resulted in lower 4-hydroxy-3-methylbut-2-enyl diphosphate reductase activity and lower contents of isopentenyl diphosphate (IPP) compared to the wild type. The transcript levels of genes involved in the syntheses of chlorophyll and thylakoid membrane proteins were significantly reduced in the ygl3 mutant compared to the wild type. The phytochrome interacting factor-like gene OsPIL11 regulated chlorophyll synthesis during the de-etiolation process by directly binding to the promoter of YGL3 to activate its expression. The findings provides a theoretical basis for understanding the molecular mechanisms by which the MEP pathway regulate chloroplast development in rice.
作为类异戊二烯前体的来源,质体甲基赤藓糖醇磷酸(MEP)途径在植物发育中起着至关重要的作用。在此,我们报道了一种新型水稻(Oryza sativa L.)突变体ygl3(黄绿叶片3),与野生型相比,该突变体表现出黄绿叶片且光合效率较低,这是由于叶绿体超微结构异常和叶绿素含量降低所致。图位克隆表明,YGL3是参与MEP途径的主要基因之一,编码4-羟基-3-甲基-2-丁烯基二磷酸还原酶,该酶定位于类囊体膜。与野生型相比,ygl3植株中的单个碱基替换导致4-羟基-3-甲基-2-丁烯基二磷酸还原酶活性降低,异戊烯基二磷酸(IPP)含量降低。与野生型相比,ygl3突变体中参与叶绿素和类囊体膜蛋白合成的基因转录水平显著降低。类光敏色素相互作用因子样基因OsPIL11通过直接结合YGL3启动子来激活其表达,从而在去黄化过程中调节叶绿素合成。这些发现为理解MEP途径调控水稻叶绿体发育的分子机制提供了理论依据。