Ye X, Wang Z -Y, Wu X, Potrykus I, Spangenberg G
Institute for Plant Sciences, Swiss Federal Institute of Technology, CH-8092, Zürich, Switzerland.
Plant Cell Rep. 1997 Mar;16(6):379-384. doi: 10.1007/BF01146777.
Transgenic forage-type Italian ryegrass (Lolium multiflorum Lam.) plants have been obtained by microprojectile bombardment of embryogenic suspension cells using a chimeric hygromycin phosphotransferase (hph) gene construct driven by riceActl 5' regulatory sequences. Parameters for the bombardment of embryogenic suspension cultures with the particle inflow gun were partially optimized using transient expression assays of a chimericβ-glucuronidase (gusA) gene driven by the maizeUbi1 promoter. Stably transformed clones were recovered with a selection scheme using hygromycin in liquid medium followed by a plate selection. Plants were regenerated from 33% of the hygromycin-resistant calli. The transgenic nature of the regenerated plants was demonstrated by Southern hybridization analysis. Expression of the transgene in transformed adult Italian ryegrass plants was confirmed by northern analysis and a hygromycin phosphotransferase enzyme assay.
利用由水稻Act1 5'调控序列驱动的嵌合潮霉素磷酸转移酶(hph)基因构建体,通过微弹轰击胚性悬浮细胞,获得了转基因饲用型意大利黑麦草(多花黑麦草)植株。使用由玉米Ubi1启动子驱动的嵌合β-葡萄糖醛酸酶(gusA)基因的瞬时表达分析,对粒子流入枪轰击胚性悬浮培养物的参数进行了部分优化。通过在液体培养基中使用潮霉素进行选择,然后进行平板选择的方案,获得了稳定转化的克隆。33%的潮霉素抗性愈伤组织再生出植株。通过Southern杂交分析证明了再生植株的转基因性质。通过Northern分析和潮霉素磷酸转移酶酶活性测定,证实了转基因在转化的成年意大利黑麦草植株中的表达。