Errampalli D., Patton D., Castle L., Mickelson L., Hansen K., Schnall J., Feldmann K., Meinke D.
Department of Botany, Oklahoma State University, Stillwater, Oklahoma 74078.
Plant Cell. 1991 Feb;3(2):149-157. doi: 10.1105/tpc.3.2.149.
T-DNA insertional mutagenesis represents a promising approach to the molecular isolation of genes with essential functions during plant embryo development. We describe in this report the isolation and characterization of 18 mutants of Arabidopsis thaliana defective in embryo development following seed transformation with Agrobacterium tumefaciens. Random T-DNA insertion was expected to result in a high frequency of recessive embryonic lethals because many target genes are required for embryogenesis. The cointegrate Ti plasmid used in these experiments contained the nopaline synthase and neomycin phosphotransferase gene markers. Nopaline assays and resistance to kanamycin were used to estimate the number of functional inserts present in segregating families. Nine families appeared to contain a T-DNA insert either within or adjacent to the mutant gene. Eight families were clearly not tagged with a functional insert and appeared instead to contain mutations induced during the transformation process. DNA gel blot hybridization with internal and right border probes revealed a variety of rearrangements associated with T-DNA insertion. A general strategy is presented to simplify the identification of tagged embryonic mutants and facilitate the molecular isolation of genes required for plant embryogenesis.
T-DNA插入诱变是一种很有前景的方法,可用于分子分离在植物胚胎发育过程中具有重要功能的基因。在本报告中,我们描述了用根癌农杆菌转化种子后,对18个拟南芥胚胎发育缺陷突变体的分离和鉴定。由于胚胎发生需要许多靶基因,随机T-DNA插入预计会导致高频隐性胚胎致死。这些实验中使用的共整合Ti质粒含有胭脂碱合酶和新霉素磷酸转移酶基因标记。通过胭脂碱测定和对卡那霉素的抗性来估计分离群体中存在的功能性插入片段的数量。九个家系似乎在突变基因内部或附近含有一个T-DNA插入。八个家系显然没有被功能性插入片段标记,而是似乎含有转化过程中诱导产生的突变。用内部和右边界探针进行的DNA凝胶印迹杂交揭示了与T-DNA插入相关的各种重排。本文提出了一种通用策略,以简化标记胚胎突变体的鉴定,并促进植物胚胎发生所需基因的分子分离。