Nowak K, Luniak N, Meyer S, Schulze J, Mendel R R, Hänsch R
Institut für Pflanzenbiologie, Technische Universität Braunschweig, Braunschweig, Germany.
Plant Biol (Stuttg). 2004 Jan-Feb;6(1):65-73. doi: 10.1055/s-2004-815730.
The jellyfish (Aequorea victoria) green fluorescent protein (GFP) and its variants (CFP [cyan] and YFP [yellow]) were successfully used as a vital marker system for the transformation of hybrid poplar (Populus tremula x P. alba). Our results show that, in this woody plant, fluorescent proteins can be expressed: (i) transiently in protoplasts after PEG-mediated transformation, as well as in leaf cells after particle bombardment, and (ii) stably in callus cells and plants after Agrobacterium-mediated transformation. For these studies, we constructed vectors permitting easy recloning of any promoter fragments of interest. Confocal laser scanning microscopy was used both for visualization and differentiation between the different colours of the GFP variants and autofluorescence of chlorophyll and lignified xylem vessels. Peroxisomes were chosen as target organelles for GFP translocation via the peroxisomal targeting sequence PTS1 because this allowed us to concentrate the fluorochrome in the small volume of a few peroxisomes, giving a bright fluorescence over background noise.
水母(维多利亚多管水母)绿色荧光蛋白(GFP)及其变体(CFP[青色]和YFP[黄色])已成功用作杂种杨树(欧洲山杨×银白杨)转化的活体标记系统。我们的结果表明,在这种木本植物中,荧光蛋白能够:(i)在聚乙二醇介导的原生质体转化后瞬时表达,以及在粒子轰击后的叶细胞中瞬时表达,(ii)在农杆菌介导的转化后在愈伤组织细胞和植株中稳定表达。为进行这些研究,我们构建了便于重新克隆任何感兴趣启动子片段的载体。共聚焦激光扫描显微镜用于GFP变体不同颜色的可视化及区分,以及叶绿素和木质化木质部导管的自发荧光。过氧化物酶体被选为通过过氧化物酶体靶向序列PTS1进行GFP易位的靶细胞器,因为这使我们能够将荧光染料集中在少数几个过氧化物酶体的小体积中,从而在背景噪声之上产生明亮的荧光。