Hatakeyama M, Sumitani M
Developmental Mechanisms Laboratory, Developmental Biology Department, National Institute of Agrobiological Sciences, Owashi, Tsukuba, Japan.
Insect Mol Biol. 2005 Jan;14(1):105-9. doi: 10.1111/j.1365-2583.2004.00526.x.
Germline transformation using a piggyBac-derived vector is feasible in the sawfly, Athalia rosae. A previously generated transgenic line carrying green fluorescence protein (GFP) genes as reporters was successfully maintained and preserved without consecutive rearing. Sperm taken from males that were frozen directly in liquid nitrogen and stored at -80 degrees C for a year were microinjected into mature unfertilized eggs dissected from female ovaries. A fraction of the sperm-injected eggs was fertilized and developed into diploid females, and all of them expressed GFP. Haploid male progeny from these females segregated into GFP-positive and GFP-negative individuals in a ratio of 1:1 indicating heterozygosity of the parental females. The GFP genes were stably inherited staying at the location where they were originally integrated.
使用源自piggyBac的载体进行种系转化在叶蜂Athalia rosae中是可行的。先前产生的携带绿色荧光蛋白(GFP)基因作为报告基因的转基因品系成功得以维持和保存,无需连续饲养。将直接在液氮中冷冻并在-80℃储存一年的雄性叶蜂的精子显微注射到从雌性卵巢中解剖出的成熟未受精卵中。一部分注射了精子的卵受精并发育成二倍体雌性,并且所有这些雌性都表达GFP。这些雌性产生的单倍体雄性后代以1:1的比例分离为GFP阳性和GFP阴性个体,表明亲本雌性是杂合子。GFP基因稳定遗传,保持在其最初整合的位置。