Jarvis P, Belzile F, Page T, Dean C
Department of Molecular Genetics, John Innes Centre, Norwich Research Park, Colney, UK.
Plant J. 1997 May;11(5):907-19.
The maize transposable element Ac is highly active in the heterologous hosts tobacco and tomato, but shows very much reduced levels of activity in Arabidopsis. A mutagenesis experiment was undertaken with the aim of identifying Arabidopsis host factors responsible for the observed low levels of Ac activity. Seed from a line carrying a single copy of the Ac element inserted into the streptomycin phosphotransferase (SPT) reporter fusion, and which displayed typically low levels of Ac activity, were mutagenized using gamma rays. Nineteen mutants displaying high levels of somatic Ac activity, as judged by their highly variegated phenotypes, were isolated after screening the M2 generation on streptomycin-containing medium. The mutations fall into two complementation groups, iae1 and iae2, are unlinked to the SPT::Ac locus and segregate in a Mendelian fashion. The iae1 mutation is recessive and the iae2 mutation is semi-dominant. The iae1 and iae2 mutants show 550- and 70-fold increases, respectively, in the average number of Ac excision sectors per cotyledon. The IAE1 locus maps to chromosome 2, whereas the SPT::Ac reporter maps to chromosome 3. A molecular study of Ac activity in the iae1 mutant confirmed the very high levels of Ac excision predicted using the phenotypic assay, but revealed only low levels of Ac re-insertion. Analyses of germinal transposition in the iae1 mutant demonstrated an average germinal excision frequency of 3% and a frequency of independent Ac re-insertions following germinal excision of 22%. The iae mutants represents a possible means of improving the efficiency of Ac/Ds transposon tagging systems in Arabidopsis, and will enable the dissection of host involvement in Ac transposition and the mechanisms employed for controlling transposable element activity.
玉米转座因子Ac在异源宿主烟草和番茄中高度活跃,但在拟南芥中的活性水平却大幅降低。开展了一项诱变实验,旨在鉴定导致所观察到的Ac低活性水平的拟南芥宿主因子。将携带单个插入链霉素磷酸转移酶(SPT)报告基因融合体的Ac元件拷贝且表现出典型低Ac活性水平的品系的种子,用伽马射线进行诱变。在含链霉素的培养基上筛选M2代后,分离出19个表现出高体细胞Ac活性的突变体,其依据是它们高度斑驳化的表型。这些突变分为两个互补群,iae1和iae2,与SPT::Ac位点不连锁,且以孟德尔方式分离。iae1突变是隐性的,iae2突变是半显性的。iae1和iae2突变体的子叶中Ac切除扇形区的平均数量分别增加了550倍和70倍。IAE1位点定位于第2号染色体,而SPT::Ac报告基因定位于第3号染色体。对iae1突变体中Ac活性的分子研究证实了通过表型分析预测的非常高的Ac切除水平,但仅揭示了低水平的Ac重新插入。对iae1突变体中生殖转座进行的分析表明,平均生殖切除频率为3%,生殖切除后独立Ac重新插入的频率为22%。iae突变体代表了提高拟南芥中Ac/Ds转座子标签系统效率的一种可能方法,并将有助于剖析宿主在Ac转座中的参与情况以及用于控制转座因子活性的机制。