Chiu W, Niwa Y, Zeng W, Hirano T, Kobayashi H, Sheen J
Department of Molecular Biology, Massachusetts General Hospital, Boston, Massachusetts 02114, USA.
Curr Biol. 1996 Mar 1;6(3):325-30. doi: 10.1016/s0960-9822(02)00483-9.
The green-fluorescent protein (GFP) of the jellyfish Aequorea victoria has recently been used as a universal reporter in a broad range of heterologous living cells and organisms. Although successful in some plant transient expression assays based on strong promoters or high copy number viral vectors, further improvement of expression efficiency and fluorescent intensity are required for GFP to be useful as a marker in intact plants. Here, we report that an extensively modified GFP is a versatile and sensitive reporter in a variety of living plant cells and in transgenic plants.
We show that a re-engineered GFP gene sequence, with the favored codons of highly expressed human proteins, gives 20-fold higher GFP expression in maize leaf cells than the original jellyfish GFP sequence. When combined with a mutation in the chromophore, the replacement of the serine at position 65 with a threonine, the new GFP sequence gives more than 100-fold brighter fluorescent signals upon excitation with 490 nm (blue) light, and swifter chromophore formation. We also show that this modified GFP has a broad use in various transient expression systems, and allows the easy detection of weak promoter activity, visualization of protein targeting into the nucleus and various plastids, and analysis of signal transduction pathways in living single cells and in transgenic plants.
The modified GFP is a simple and economical new tool for the direct visualization of promoter activities with a broad range of strength and cell specificity. It can be used to measure dynamic responses of signal transduction pathways, transfection efficiency, and subcellular localization of chimeric proteins, and should be suitable for many other applications in genetically modified living cells and tissues of higher plants. The data also suggest that the codon usage effect might be universal, allowing the design of recombinant proteins with high expression efficiency in evolutionarily distant species such as humans and maize.
维多利亚多管水母的绿色荧光蛋白(GFP)最近已被用作广泛的异源活细胞和生物体中的通用报告基因。尽管在一些基于强启动子或高拷贝数病毒载体的植物瞬时表达试验中取得了成功,但要使GFP作为完整植物中的标记物,还需要进一步提高其表达效率和荧光强度。在此,我们报道一种经过广泛修饰的GFP在多种活植物细胞和转基因植物中是一种通用且灵敏的报告基因。
我们表明,一个重新设计的GFP基因序列,采用了高表达人类蛋白所偏好的密码子,在玉米叶细胞中的GFP表达量比原始的水母GFP序列高20倍。当与发色团中的一个突变相结合,即将第65位的丝氨酸替换为苏氨酸时,新的GFP序列在用490nm(蓝色)光激发时会产生比原来亮100倍以上的荧光信号,并且发色团形成更快。我们还表明,这种修饰后的GFP在各种瞬时表达系统中具有广泛用途,能够轻松检测弱启动子活性、观察蛋白质靶向细胞核和各种质体的过程,以及分析活单细胞和转基因植物中的信号转导途径。
修饰后的GFP是一种简单且经济的新工具,可直接可视化具有广泛强度和细胞特异性的启动子活性。它可用于测量信号转导途径的动态响应、转染效率以及嵌合蛋白的亚细胞定位,并且应该适用于高等植物转基因活细胞和组织中的许多其他应用。数据还表明密码子使用效应可能具有普遍性,这使得在进化距离较远的物种如人类和玉米中设计具有高表达效率的重组蛋白成为可能。