Mookkan Muruganantham, Nelson-Vasilchik Kimberly, Hague Joel, Kausch Albert, Zhang Zhanyuan J
Division of Plant Sciences, University of Missouri, Columbia, Missouri.
Department of Cell and Molecular Biology, University of Rhode Island, Kingston, Rhode Island.
Curr Protoc Plant Biol. 2018 Dec;3(4):e20075. doi: 10.1002/cppb.20075. Epub 2018 Oct 22.
Maize B73 is a reference genome and has long been a major resource for genetics and molecular biology research. We have developed an efficient B73 transformation protocol by enabling somatic embryogenesis through differential co-expression of maize morphogenic regulators BBM and WUS2. We describe a successful protocol that utilizes Agrobacterium tumefaciens strain AGL1 harboring binary vector PHP78891 that comprises a BBM and WUS2 expression cassette as well as a green fluorescent protein (GFP) reporter cassette. The PHP78891 vector also contains, within the T-DNA region, a CRE/lox recombination system flanking the CRE/BBM/WUS2 co-expression cassette driven by the desiccation inducible RAB17 promoter that allows removal of the BBM/WUS2 cassette. Introduction and co-expression of BBM and WUS2 induced direct somatic embryogenesis (SE) in non-regenerable maize B73 from immature embryo explants. Removal of the CRE/BBM/WUS2 cassette is essential to allow regeneration to fertile plants. The GFP expression cassette outside the lox excision sites is retained in the transgenic plant genome, allowing subsequent phenotypic analysis of calli and regenerated transgenic events. This transformation system enables a selectable marker-free transformation process by taking advantage of BBM/WUS2-induced SE as a developmental selection system. © 2018 by John Wiley & Sons, Inc.
玉米B73是一个参考基因组,长期以来一直是遗传学和分子生物学研究的主要资源。我们通过玉米形态发生调节因子BBM和WUS2的差异共表达实现体细胞胚胎发生,从而开发出一种高效的B73转化方案。我们描述了一种成功的方案,该方案利用携带二元载体PHP78891的根癌农杆菌AGL1菌株,该载体包含一个BBM和WUS2表达盒以及一个绿色荧光蛋白(GFP)报告盒。PHP78891载体在T-DNA区域内还包含一个CRE/lox重组系统,该系统位于由干燥诱导型RAB17启动子驱动的CRE/BBM/WUS2共表达盒两侧,允许去除BBM/WUS2盒。BBM和WUS2的导入和共表达在未成熟胚外植体的不可再生玉米B73中诱导了直接体细胞胚胎发生(SE)。去除CRE/BBM/WUS2盒对于使植株再生为可育植株至关重要。lox切除位点外的GFP表达盒保留在转基因植物基因组中,从而允许对愈伤组织和再生的转基因事件进行后续表型分析。该转化系统通过利用BBM/WUS2诱导的SE作为发育选择系统,实现了无选择标记的转化过程。© 2018约翰威立父子公司。