Wu Jianxin, Qiu Shijun, Wang Menglong, Xu Chunjue, Deng Xing Wang, Tang Xiaoyan
Guangdong Provincial Key Laboratory of Biotechnology for Plant Development, School of Life Sciences, South China Normal University, 510631, Guangzhou, China.
Shenzhen Institute of Molecular Crop Design, 518107, Shenzhen, China.
Rice (N Y). 2021 Jul 13;14(1):66. doi: 10.1186/s12284-021-00510-y.
The third-generation hybrid rice technology can be constructed by transforming a recessive nuclear male sterile (NMS) mutant with a transgenic cassette containing three functional modules: the wild type male fertility gene to restore the fertility of the mutant, the pollen killer gene that specifically kills the pollen grains carrying the transgene, and the red fluorescence protein (RFP) gene to mark the transgenic seed (maintainer). The transgenic plant produces 1:1 NMS seeds and maintainer seeds that can be distinguished by the RFP signal. However, the RFP signals in the partially filled or pathogen-infected maintainer seeds are often too weak to be detected by RFP-based seed sorting machine, resulting in intermingling of the maintainer seeds with NMS seeds.
Here we constructed a weight-based seed sorting system for the third-generation hybrid rice technology by silencing the genes encoding ADP-glucose pyrophosphorylase (AGP) essential for endosperm starch biosynthesis via endosperm-specific expression of artificial microRNAs (amiRNAs). In this system, the NMS seeds have normal endosperm and are heavy, but the maintainer seeds have shrunken endosperms and are light-weighted. The maintainer seeds can be easily and accurately sorted out from the NMS seeds by weight-sorting machines, so pure and fully filled NMS seeds are available.
The weight-based seed sorting system shows obvious advantages over the RFP-based seed sorting system in accuracy, efficiency, and cost for propagation of pure male sterile seeds. These characteristics will significantly increase the value and transgenic safety of the third-generation hybrid rice technology.
第三代杂交水稻技术可通过用包含三个功能模块的转基因盒转化隐性核雄性不育(NMS)突变体来构建:用于恢复突变体育性的野生型雄性育性基因、特异性杀死携带转基因的花粉粒的花粉杀手基因以及用于标记转基因种子(保持系)的红色荧光蛋白(RFP)基因。转基因植株产生1:1的NMS种子和保持系种子,可通过RFP信号进行区分。然而,部分饱满或受病原体感染的保持系种子中的RFP信号往往太弱,无法被基于RFP的种子分选机检测到,导致保持系种子与NMS种子混杂。
在此,我们通过胚乳特异性表达人工微小RNA(amiRNA)沉默对胚乳淀粉生物合成至关重要的编码ADP-葡萄糖焦磷酸化酶(AGP)的基因,构建了用于第三代杂交水稻技术的基于重量的种子分选系统。在该系统中,NMS种子具有正常胚乳且较重,而保持系种子的胚乳萎缩且重量较轻。通过重量分选机可以轻松、准确地从NMS种子中筛选出保持系种子,从而获得纯净且饱满的NMS种子。
基于重量的种子分选系统在纯雄性不育种子繁殖的准确性、效率和成本方面比基于RFP的种子分选系统具有明显优势。这些特性将显著提高第三代杂交水稻技术的价值和转基因安全性。