Li Meng, Niu Xufang, Li Shuang, Fu Shasha, Li Qianfang, Xu Meizhi, Wang Chunhua, Wu Shuang
College of Life Sciences and Horticultural Plant Biology Metabolomics Center, Fujian Agriculture and Forestry University, Fuzhou 350002, China.
Plants (Basel). 2023 Jun 19;12(12):2365. doi: 10.3390/plants12122365.
CRISPR/Cas9 (hereafter Cas9)-mediated gene knockout is one of the most important tools for studying gene function. However, many genes in plants play distinct roles in different cell types. Engineering the currently used Cas9 system to achieve cell-type-specific knockout of functional genes is useful for addressing the cell-specific functions of genes. Here we employed the cell-specific promoters of the (), (), and () genes to drive the Cas9 element, allowing tissue-specific targeting of the genes of interest. We designed the reporters to verify the tissue-specific gene knockout in vivo. Our observation of the developmental phenotypes provides strong evidence for the involvement of () and () in the development of quiescent center (QC) and endodermal cells. This system overcomes the limitations of traditional plant mutagenesis techniques, which often result in embryonic lethality or pleiotropic phenotypes. By allowing cell-type-specific manipulation, this system has great potential to help us better understand the spatiotemporal functions of genes during plant development.
CRISPR/Cas9(以下简称Cas9)介导的基因敲除是研究基因功能的最重要工具之一。然而,植物中的许多基因在不同细胞类型中发挥着不同的作用。改造当前使用的Cas9系统以实现功能基因的细胞类型特异性敲除,对于研究基因的细胞特异性功能很有帮助。在这里,我们利用了()、()和()基因的细胞特异性启动子来驱动Cas9元件,从而实现对感兴趣基因的组织特异性靶向。我们设计了报告基因来验证体内的组织特异性基因敲除。我们对发育表型的观察为()和()参与静止中心(QC)和内胚层细胞的发育提供了有力证据。该系统克服了传统植物诱变技术的局限性,传统技术常常导致胚胎致死或多效性表型。通过允许细胞类型特异性操作,该系统具有巨大潜力,可帮助我们更好地理解植物发育过程中基因的时空功能。