Xu Dawei, Mondol Palash Chandra, Uzair Muhammad, Tucker Matthew R, Zhang Dabing
Joint International Research Laboratory of Metabolic and Developmental Sciences, Shanghai Jiao Tong University-University of Adelaide Joint Centre for Agriculture and Health, School of Life Sciences and Biotechnology, Shanghai Jiao Tong University; College of Agronomy, Anhui Agricultural University, Heifei, China;
Joint International Research Laboratory of Metabolic and Developmental Sciences, Shanghai Jiao Tong University-University of Adelaide Joint Centre for Agriculture and Health, School of Life Sciences and Biotechnology, Shanghai Jiao Tong University.
J Vis Exp. 2020 Oct 6(164). doi: 10.3791/61665.
Male sterility is an important agronomic trait for hybrid seed production that is usually characterized by functional defects in male reproductive organs/gametes. Recent advances in CRISPR-Cas9 genome editing technology allow for high editing efficacy and timesaving knockout mutations of endogenous candidate genes at specific sites. Additionally, Agrobacterium-mediated genetic transformation of rice is also a key method for gene modification, which has been widely adopted by many public and private laboratories. In this study, we applied CRISPR-Cas9 genome editing tools and successfully generated three male sterile mutant lines by targeted genome editing of OsABCG15 in a japonica cultivar. We used a modified Agrobacterium-mediated rice transformation method that could provide excellent means of genetic emasculation for hybrid seed production in rice. Transgenic plants can be obtained within 2-3 months and homozygous transformants were screened by genotyping using PCR amplification and Sanger sequencing. Basic phenotypic characterization of the male sterile homozygous line was performed by microscopic observation of the rice male reproductive organs, pollen viability analysis by iodine potassium iodide (I2-KI) staining semi-thin cross-sectioning of developing anthers.
雄性不育是杂交种子生产中的一个重要农艺性状,通常表现为雄性生殖器官/配子的功能缺陷。CRISPR-Cas9基因组编辑技术的最新进展使得在特定位点对内源候选基因进行高效编辑和省时的敲除突变成为可能。此外,农杆菌介导的水稻遗传转化也是基因修饰的关键方法,已被许多公共和私人实验室广泛采用。在本研究中,我们应用CRISPR-Cas9基因组编辑工具,通过对粳稻品种中OsABCG15进行靶向基因组编辑,成功获得了三个雄性不育突变系。我们使用了一种改良的农杆菌介导的水稻转化方法,该方法可为水稻杂交种子生产提供优良的遗传去雄手段。转基因植株可在2-3个月内获得,并通过PCR扩增和Sanger测序进行基因分型筛选纯合转化体。通过对水稻雄性生殖器官的显微镜观察、用碘化钾(I2-KI)染色分析花粉活力以及对发育中的花药进行半薄切片,对雄性不育纯合系进行了基本的表型特征分析。