Koga Akihiko, Hori Hiroshi, Sakaizumi Mitsuru
Division of Biological Sciences, Graduate School of Science, Nagoya University, Nagoya 464-8602, Japan.
Mar Biotechnol (NY). 2002 Jan;4(1):6-11. doi: 10.1007/s10126-001-0086-2.
For the ultimate purpose of developing genetic tools using the medaka fish Tol2 transposable element, we examined whether it can transfer a marker gene into the fish genome and also be applied for cloning of chromosomal regions adjacent to insertion points. An internal region of Tol2 was removed and replaced with the green fluorescent protein (GFP) gene and a bacterial plasmid replication origin. This modified Tol2 clone was microinjected into fertilized eggs together with messenger RNA for the Tol2 transposase. The GFP gene was found to be integrated into chromosomes and transmitted to subsequent generations. Restriction enzyme digestion of genomic DNA of a transformant fish, followed by ligation and introduction into bacteria, produced a plasmid containing the entire element and flanking chromosomal regions. Sequencing analysis of this clone demonstrated transposition of the element in the germline of the first generation. Thus, the basic requirements for a gene transfer vector and gene tagging system were fulfilled.
为了利用青鳉鱼Tol2转座子开发遗传工具这一最终目的,我们研究了它是否能将标记基因转移到鱼的基因组中,以及是否可用于克隆插入点附近的染色体区域。去除了Tol2的内部区域,并用绿色荧光蛋白(GFP)基因和细菌质粒复制起点取而代之。将这个经过修饰的Tol2克隆与Tol2转座酶的信使RNA一起显微注射到受精卵中。发现GFP基因整合到了染色体中并传递给了后代。对转基因鱼的基因组DNA进行限制性酶切,然后连接并导入细菌,产生了一个包含整个元件和侧翼染色体区域的质粒。对这个克隆进行测序分析表明该元件在第一代种系中发生了转座。因此,满足了基因转移载体和基因标签系统的基本要求。