Key Laboratory of Crop Heterosis and Utilization (MOE) of Ministry of Education, Beijing Key Laboratory of Crop Genetic Improvement, China Agricultural University, Beijing 100193, China.
Beijing Engineering Research Center for Hybrid Wheat, Beijing Academy of Agricultural and Forestry Sciences, Beijing 100097, China.
Int J Mol Sci. 2020 May 5;21(9):3257. doi: 10.3390/ijms21093257.
Starch and prolamin composition and content are important indexes for determining the processing and nutritional quality of wheat ( L.) grains. Several transcription factors (TFs) regulate gene expression during starch and protein biosynthesis in wheat. Storage protein activator (TaSPA), a member of the basic leucine zipper (bZIP) family, has been reported to activate glutenin genes and is correlated to starch synthesis related genes. In this study, we generated overexpressing (OE) transgenic wheat lines. Compared with wild-type (WT) plants, the starch content was slightly reduced and starch granules exhibited a more polarized distribution in the OE lines. Moreover, glutenin and ω- gliadin contents were significantly reduced, with lower expression levels of related genes (e.g., , and ω-1,2 gliadin gene). RNA-seq analysis identified 2023 differentially expressed genes (DEGs). The low expression of some DEGs (e.g., , , , , , , and ) might explain the reduction of starch contents. Some TFs involved in glutenin and starch synthesis might be regulated by for example, was reduced in OE-3 lines. In addition, dual-luciferase reporter assay indicated that both TaSPA-B and TaPBF could transactivate the promoter of ω-1,2 gliadin gene. These results suggest that regulates a complex gene network and plays an important role in starch and protein biosynthesis in wheat.
淀粉和醇溶蛋白的组成和含量是决定小麦(L.)谷物加工和营养价值的重要指标。几个转录因子(TFs)在小麦淀粉和蛋白质生物合成过程中调节基因表达。贮藏蛋白激活子(TaSPA),作为碱性亮氨酸拉链(bZIP)家族的一员,已被报道能激活麦谷蛋白基因,并与淀粉合成相关基因相关。在本研究中,我们生成了过表达(OE)的转基因小麦品系。与野生型(WT)植株相比,OE 系的淀粉含量略有降低,淀粉粒呈更极化分布。此外,麦谷蛋白和ω-醇溶蛋白含量显著降低,相关基因的表达水平较低(例如,、、和ω-1,2 醇溶蛋白基因)。RNA-seq 分析鉴定了 2023 个差异表达基因(DEGs)。一些 DEGs(例如、、、、、、和)的低表达可能解释了淀粉含量的降低。一些参与麦谷蛋白和淀粉合成的 TFs 可能受到的调节,例如,OE-3 系中 表达降低。此外,双荧光素酶报告基因 assay 表明 TaSPA-B 和 TaPBF 均可转录激活ω-1,2 醇溶蛋白基因的启动子。这些结果表明,通过调控一个复杂的基因网络,在小麦淀粉和蛋白质生物合成中发挥重要作用。