Yazawa Ryosuke, Hirono Ikuo, Ohira Tsuyoshi, Aoki Takashi
Graduate School of Marine Science and Technology, Tokyo University of Marine Science and Technology, Konan 4-5-7, Minato, Tokyo, 108-8477, Japan.
Mar Biotechnol (NY). 2005 May-Jun;7(3):231-5. doi: 10.1007/s10126-004-0403-7. Epub 2005 May 5.
A recombinant plasmid containing the 2381-bp promoter region of Japanese flounder tumor necrosis factor (TNF) and green fluorescence protein (GFP) was introduced into zebrafish fertilized eggs by microinjection. GFP was expressed in 2 transgenic zebrafish lines in the heart and around the pharynx under unstressed condition. When embryos were exposed to lipopolysaccharide (LPS), GFP was expressed in the whole zebrafish embryonic surface, and Western blot analysis also showed that the level of the expressed GFP protein in zebrafish embryo was higher at an LPS concentration of 140 microg/ml than at LPS concentrations of 0 and 70 microg/ml. Stimulation with either concanavalin A or phorbol myristate acetate induced weak GFP expression, but stimulation with both of them induced strong expression similar to that induced by LPS. GFP expression peaked 1 hour after stimulation, then gradually decreased. These results indicate that transcription regulated by the Japanese flounder TNF promoter could be under the control of the LPS-recognition system in zebrafish embryos.
通过显微注射将含有牙鲆肿瘤坏死因子(TNF)2381 bp启动子区域和绿色荧光蛋白(GFP)的重组质粒导入斑马鱼受精卵。在未受应激条件下,GFP在2个转基因斑马鱼品系的心脏和咽部周围表达。当胚胎暴露于脂多糖(LPS)时,GFP在整个斑马鱼胚胎表面表达,蛋白质免疫印迹分析还显示,在LPS浓度为140 μg/ml时,斑马鱼胚胎中表达的GFP蛋白水平高于LPS浓度为0和70 μg/ml时。用刀豆球蛋白A或佛波酯刺激诱导较弱的GFP表达,但两者同时刺激诱导的强表达类似于LPS诱导的表达。刺激后1小时GFP表达达到峰值,然后逐渐下降。这些结果表明,牙鲆TNF启动子调控的转录可能受斑马鱼胚胎中LPS识别系统的控制。