Wang Menglong, Yan Wei, Peng Xiaoqun, Chen Zhufeng, Xu Chunjue, Wu Jianxin, Deng Xing Wang, Tang Xiaoyan
Guangdong Provincial Key Laboratory of Biotechnology for Plant Development, School of Life Sciences, South China Normal University, Guangzhou, 510631, China.
Shenzhen Institute of Molecular Crop Design, Shenzhen, 518107, China.
J Integr Plant Biol. 2020 Aug;62(8):1246-1263. doi: 10.1111/jipb.12912. Epub 2020 Feb 20.
Large-scale production of male sterile seeds can be achieved by introducing a fertility-restoration gene linked with a pollen-killer gene into a recessive male sterile mutant. We attempted to construct this system in rice by using a late-stage pollen-specific (LSP) promoter driving the expression of maize α-amylase gene ZM-AA1. To obtain such promoters in rice, we conducted comparative RNA-seq analysis of mature pollen with meiosis anther, and compared this with the transcriptomic data of various tissues in the Rice Expression Database, resulting in 269 candidate LSP genes. Initial test of nine LSP genes showed that only the most active OsLSP3 promoter could drive ZM-AA1 to disrupt pollen. We then analyzed an additional 22 LSP genes and found 12 genes stronger than OsLSP3 in late-stage anthers. The promoters of OsLSP5 and OsLSP6 showing higher expression than OsLSP3 at stages 11 and 12 could drive ZM-AA1 to inactivate pollen, while the promoter of OsLSP4 showing higher expression at stage 12 only could not drive ZM-AA1 to disrupt pollen, suggesting that strong promoter activity at stage 11 was critical for pollen inactivation. The strong pollen-specific promoters identified in this study provided valuable tools for genetic engineering of rice male sterile system for hybrid rice production.
通过将与花粉致死基因连锁的育性恢复基因导入隐性雄性不育突变体中,可以实现大规模生产雄性不育种子。我们试图通过使用驱动玉米α-淀粉酶基因ZM-AA1表达的晚期花粉特异性(LSP)启动子在水稻中构建该系统。为了在水稻中获得此类启动子,我们对成熟花粉与减数分裂期花药进行了比较RNA测序分析,并将其与水稻表达数据库中各种组织的转录组数据进行比较,从而得到了269个候选LSP基因。对9个LSP基因的初步测试表明,只有活性最强的OsLSP3启动子能够驱动ZM-AA1破坏花粉。然后我们分析了另外22个LSP基因,发现有12个基因在晚期花药中的活性比OsLSP3更强。在第11和12阶段表达高于OsLSP3的OsLSP5和OsLSP6启动子能够驱动ZM-AA1使花粉失活,而仅在第12阶段表达较高的OsLSP4启动子不能驱动ZM-AA1破坏花粉,这表明第11阶段的强启动子活性对于花粉失活至关重要。本研究中鉴定出的强花粉特异性启动子为用于杂交水稻生产的水稻雄性不育系统的基因工程提供了有价值的工具。