Lee Yeo Jin, Kim Jae Kwang, Baek Seung-A, Yu Ji-Su, You Min Kyoung, Ha Sun-Hwa
Department of Genetics and Biotechnology, Graduate School of Biotechnology, College of Life Sciences, Kyung Hee University, Yongin, South Korea.
Division of Life Sciences, Bio-Resource and Environmental Center, Incheon National University, Incheon, South Korea.
Front Plant Sci. 2022 Apr 13;13:861036. doi: 10.3389/fpls.2022.861036. eCollection 2022.
The methylerythritol 4-phosphate (MEP) pathway is responsible for providing common precursors for the biosynthesis of diverse plastidial terpenoids, including chlorophylls, carotenoids, and phytohormones, in plants. In rice (), the last-step genes encoding 4-hydroxy-3-methylbut-2-enyl diphosphate reductase [HDR/isoprenoid synthesis H (IspH)] have been annotated in two genes ( and ) in the rice genome. The spatial transcript levels indicated that is highly expressed in all tissues at different developmental stages, whereas is barely expressed due to an early stop in exon 1 caused by splicing error. OsIspH1 localized into plastids and , a T-DNA inserted knockout mutant, showed an albino phenotype, indicating that is the only functional gene. To elucidate the role of in the MEP pathway, we created two single (H145P and K407R) and double (H145P/K407R) mutations and performed complementation tests in two mutants, including DLYT1 strains and rice plants. The results showed that every single mutation retained HDR function, but a double mutation lost it, proposing that the complementary relations of two residues might be important for enzyme activity but not each residue. When overexpressed in rice plants, the double-mutated gene, , reduced chlorophyll and carotenoid biosynthesis in the leaves and seeds. It confirmed the crucial role of in plastidic terpenoid biosynthesis, revealing organ-specific differential regulation of in rice plants.
甲基赤藓糖醇4-磷酸(MEP)途径负责为植物中多种质体类萜的生物合成提供常见前体,包括叶绿素、类胡萝卜素和植物激素。在水稻中,编码4-羟基-3-甲基丁-2-烯基二磷酸还原酶[HDR/类异戊二烯合成H(IspH)]的最后一步基因在水稻基因组中的两个基因( 和 )中已被注释。空间转录水平表明, 在不同发育阶段的所有组织中均高度表达,而 由于剪接错误导致外显子1提前终止而几乎不表达。OsIspH1定位于质体, ,一个T-DNA插入敲除突变体,表现出白化表型,表明 是唯一的功能基因。为了阐明 在MEP途径中的作用,我们创建了两个单突变(H145P和K407R)和双突变(H145P/K407R),并在两个 突变体中进行了互补试验,包括DLYT1菌株和水稻植株。结果表明,每个单突变都保留了HDR功能,但双突变失去了该功能,这表明两个残基的互补关系可能对酶活性很重要,而不是每个残基。当在水稻植株中过表达时,双突变基因 降低了叶片和种子中叶绿素和类胡萝卜素的生物合成。这证实了 在质体类萜生物合成中的关键作用,揭示了水稻植株中 器官特异性的差异调控。