Shimizu-Sato Sae, Tsuda Katsutoshi, Nosaka-Takahashi Misuzu, Suzuki Toshiya, Ono Seijiro, Ta Kim Nhung, Yoshida Yuri, Nonomura Ken-Ichi, Sato Yutaka
National Institute of Genetics, 1111 Yata, Mishima, Shizuoka, 411-8540, Japan.
Rice (N Y). 2020 Jun 3;13(1):33. doi: 10.1186/s12284-020-00394-4.
Genetic transformation is one of the most important technologies for revealing or modulating gene function. It is used widely in both functional genomics and molecular breeding of rice. Demands on its use in wild Oryza species is increasing because of their high genetic diversity. Given the difficulties in genetic crosses between distantly related species, genetic transformation offers a way to alter or transfer genetic traits in wild rice accessions. However, transformation of wild Oryza accessions by conventional methods using calli induced from scutellum tissue of embryos in mature seeds often fails. Here, we report methods using immature embryos for the genetic transformation of a broad range of Oryza species. First, we investigated the ability of callus induction and regeneration from immature embryos of 192 accessions in 20 species under several culture conditions. We regenerated plants from immature embryos of 90 accessions in 16 species. Next, we optimized the conditions of Agrobacterium infection using a vector carrying the GFP gene driven by the maize ubiquitin promoter. GFP signals were observed in 51 accessions in 11 species. We analyzed the growth and seed set of transgenic plants of O. barthii, O. glumaepatula, O. rufipogon, and O. brachyantha. The plants grew to maturity and set seeds normally. Southern blot analyses using DNA from T plants showed that all GFP plants were derived from independent transformation events. We confirmed that the T-DNAs were transmitted to the next generation through the segregation of GFP signals in the T generation. These results show that many Oryza species can be transformed by using modified immature-embryo methods. This will accelerate the use of wild Oryza accessions in molecular genetic analyses and molecular breeding.
遗传转化是揭示或调控基因功能的最重要技术之一。它在水稻功能基因组学和分子育种中都有广泛应用。由于野生稻种具有高度的遗传多样性,对其进行遗传转化的需求日益增加。鉴于远缘物种间遗传杂交存在困难,遗传转化为改变或转移野生稻种质的遗传性状提供了一条途径。然而,利用成熟种子胚盾片组织诱导的愈伤组织通过常规方法对野生稻种质进行转化往往失败。在此,我们报道了利用未成熟胚对多种稻种进行遗传转化的方法。首先,我们研究了在几种培养条件下20个物种192份种质未成熟胚的愈伤组织诱导和再生能力。我们从16个物种90份种质的未成熟胚中再生出了植株。接下来,我们使用携带由玉米泛素启动子驱动的绿色荧光蛋白(GFP)基因的载体优化了农杆菌感染条件。在11个物种的51份种质中观察到了GFP信号。我们分析了巴氏稻、阔叶稻、普通野生稻和短药野生稻转基因植株的生长和结实情况。这些植株正常生长至成熟并结实。对T代植株DNA进行的Southern杂交分析表明,所有GFP植株均来自独立的转化事件。我们通过T代中GFP信号的分离证实T-DNA传递到了下一代。这些结果表明,利用改良的未成熟胚方法可以对许多稻种进行转化。这将加速野生稻种质在分子遗传分析和分子育种中的应用。