Jiang Qinqin, Jiang Wenhui, Hu Ning, Tang Rui, Dong Yuxuan, Wu Hongqi, Liu Tianxiang, Guan Lulu, Zhang Hanbing, Hou Junbin, Chai Guaiqiang, Wang Zhonghua
State Key Laboratory of Crop Stress Biology in Arid Areas, College of Agronomy, Northwest A&F University, Yangling 712100, China.
Shenzhen Branch, Guangdong Laboratory for Lingnan Modern Agriculture, Genome Analysis Laboratory of the Ministry of Agriculture, Agricultural Genomics Institute at Shenzhen, Chinese Academy of Agricultural Sciences, Shenzhen 518120, China.
Plants (Basel). 2023 Aug 19;12(16):2996. doi: 10.3390/plants12162996.
Purple-grained wheat ( L.) is an important germplasm source in crop breeding. Anthocyanin biosynthesis in the pericarps of purple-grained wheat is largely light-dependent; however, the regulatory mechanisms underlying light-induced anthocyanin accumulation in the wheat pericarp remain unknown. Here we determined that anthocyanins rapidly accumulate in the pericarps of the purple-grained wheat cultivar Heixiaomai 76 (H76) at 16 days after pollination under light treatment. Using transcriptome sequencing, differential gene expression analysis, and phylogenetic analysis, we identified two key genes involved in light signaling in wheat: () and (). and were highly expressed in purple-grained wheat pericarps. The heterologous expression of partially restored the phenotype of the Arabidopsis () mutant, resulting in increased anthocyanin accumulation and a shortened hypocotyl. The heterologous expression of in wild-type had similar effects. TaHY5-7A and TaBBX-3B were nucleus-localized, consistent with a function in transcription regulation. However, TaHY5-7A, which lacks a transactivation domain, was not sufficient to activate the expression of (), the key anthocyanin biosynthesis regulator in purple pericarps of wheat. TaHY5-7A physically interacted with TaBBX-3B in yeast two-hybrid and bimolecular fluorescence complementation assays. Additionally, TaHY5-7A, together with TaBBX-3B, greatly enhanced the promoter activity of in a dual luciferase assay. Overall, our results suggest that TaHY5-7A and TaBBX-3B collaboratively activate expression to promote light-induced anthocyanin biosynthesis in purple-pericarp wheat.
紫粒小麦(L.)是作物育种中的重要种质资源。紫粒小麦果皮中花青素的生物合成在很大程度上依赖光照;然而,光照诱导小麦果皮中花青素积累的调控机制仍不清楚。在这里,我们确定在授粉后16天,在光照处理下,紫粒小麦品种黑小麦76(H76)的果皮中花青素迅速积累。通过转录组测序、差异基因表达分析和系统发育分析,我们鉴定出两个参与小麦光信号传导的关键基因:()和()。和在紫粒小麦果皮中高表达。的异源表达部分恢复了拟南芥()突变体的表型,导致花青素积累增加和下胚轴缩短。在野生型中的异源表达也有类似效果。TaHY5 - 7A和TaBBX - 3B定位于细胞核,这与它们在转录调控中的功能一致。然而,缺乏反式激活结构域的TaHY5 - 7A不足以激活小麦紫色果皮中关键花青素生物合成调节因子()的表达。在酵母双杂交和双分子荧光互补试验中,TaHY5 - 7A与TaBBX - 3B发生物理相互作用。此外,在双荧光素酶试验中,TaHY5 - 7A与TaBBX - 3B一起极大地增强了的启动子活性。总体而言,我们的结果表明TaHY5 - 7A和TaBBX - 3B协同激活表达,以促进紫皮小麦中光诱导的花青素生物合成。