Guangdong Provincial Key Laboratory of Plant Resources, State Key Laboratory for Biocontrol, School of Life Sciences, Sun Yat-Sen University, Guangzhou 510275, People's Republic of China.
Guangdong Provincial Key Laboratory of Plant Resources, State Key Laboratory for Biocontrol, School of Life Sciences, Sun Yat-Sen University, Guangzhou 510275, People's Republic of China
Plant Physiol. 2017 Nov;175(3):1175-1185. doi: 10.1104/pp.17.01169. Epub 2017 Sep 13.
Increasing grain yield is the most important object of crop breeding. Here, we report that the elevated expression of a conserved microRNA, OsmiR408, could positively regulate grain yield in rice () by increasing panicle branches and grain number. We further showed that OsmiR408 regulates grain yield by down-regulating its downstream target, , which is an uclacyanin (UCL) gene of the phytocyanin family. The knock down or knock out of also increases grain yield, while the overexpression of results in an opposite phenotype. Spatial and temporal expression analyses showed that was highly expressed in pistils, young panicles, developing seeds, and inflorescence meristem and was nearly complementary to that of OsmiR408. Interestingly, the OsUCL8 protein was localized to the cytoplasm, distinct from a majority of phytocyanins, which localize to the plasma membrane. Further studies revealed that the cleavage of by miR408 affects copper homeostasis in the plant cell, which, in turn, affects the abundance of plastocyanin proteins and photosynthesis in rice. To our knowledge, this is the first report of the effects of miR408- in regulating rice photosynthesis and grain yield. Our study further broadens the perspective of microRNAs and UCLs and provides important information for breeding high-yielding crops through genetic engineering.
提高粮食产量是作物育种最重要的目标。在这里,我们报告称,保守的 microRNA OsmiR408 的表达水平升高,可通过增加穗分枝和粒数,正向调控水稻的粒重。我们进一步表明,OsmiR408 通过下调其下游靶基因 来调控粒重, 是植物蓝素家族的一个 UCL 基因。 的敲除或敲低也会增加粒重,而 的过表达则会产生相反的表型。时空表达分析表明, 在雌蕊、幼穗、发育种子和花序分生组织中高度表达,与 OsmiR408 的表达几乎互补。有趣的是,OsUCL8 蛋白定位于细胞质,与大多数植物蓝素不同,后者定位于质膜。进一步的研究表明,miR408 对 的切割影响植物细胞中的铜稳态,进而影响水稻质体蓝素蛋白和光合作用的丰度。据我们所知,这是 miR408-调控水稻光合作用和粒重的第一个报道。我们的研究进一步拓宽了 microRNAs 和 UCLs 的视角,并为通过基因工程培育高产作物提供了重要信息。