National Key Laboratory of Crop Genetic Improvement, Huazhong Agricultural University, Wuhan, 430070, China.
College of Life Science and Technology, Huazhong Agricultural University, Wuhan, 430070, China.
New Phytol. 2019 Jul;223(1):261-276. doi: 10.1111/nph.15801. Epub 2019 Apr 20.
Diacylglycerol kinase (DGK) phosphorylates diacylglycerol (DAG) to generate phosphatidic acid (PA), and both DAG and PA are lipid mediators in the cell. Here we show that DGK1 in rice (Oryza sativa) plays important roles in root growth and development. Two independent OsDGK1-knockout (dgk1) lines exhibited a higher density of lateral roots (LRs) and thinner seminal roots (SRs), whereas OsDGK1-overexpressing plants displayed a lower LR density and thicker SRs than wild-type (WT) plants. Overexpression of OsDGK1 led to a decline in the DGK substrate DAG whereas specific PA species decreased in dgk1 roots. Supplementation of DAG to OsDGK1-overexpressing seedlings restored the LR density and SR thickness whereas application of PA to dgk1 seedlings restored the LR density and SR thickness to those of the WT. In addition, treatment of rice seedlings with the DGK inhibitor R59022 increased the level of DAG and decreased PA, which also restored the root phenotype of OsDGK1-overexpressing seedlings close to that of the WT. Together, these results indicate that DGK1 and associated lipid mediators modulate rice root architecture; DAG promotes LR formation and suppresses SR growth whereas PA suppresses LR number and promotes SR thickness.
二酰基甘油激酶(DGK)将二酰基甘油(DAG)磷酸化为磷酸脂酸(PA),DAG 和 PA 都是细胞中的脂质介质。在这里,我们表明水稻中的 DGK1(Oryza sativa)在根生长和发育中发挥重要作用。两个独立的 OsDGK1 敲除(dgk1)系表现出更高密度的侧根(LRs)和更细的主根(SRs),而 OsDGK1 过表达植物的 LR 密度低于野生型(WT)植物,SRs 较厚。OsDGK1 的过表达导致 DGK 底物 DAG 的减少,而特定的 PA 物种在 dgk1 根中减少。向 OsDGK1 过表达幼苗中添加 DAG 恢复了 LR 密度和 SR 厚度,而向 dgk1 幼苗中添加 PA 则将 LR 密度和 SR 厚度恢复到 WT 的水平。此外,用 DGK 抑制剂 R59022 处理水稻幼苗会增加 DAG 的水平并降低 PA 的水平,这也使 OsDGK1 过表达幼苗的根表型接近于 WT。总之,这些结果表明 DGK1 和相关的脂质介质调节水稻的根系结构;DAG 促进 LR 的形成并抑制 SR 的生长,而 PA 则抑制 LR 的数量并促进 SR 的厚度。