Schetelig Marc F, Handler Alfred M
USDA/ARS, Center for Medical, Agricultural and Veterinary Entomology, 1700 SW 23rd Drive, Gainesville, FL 32608, USA.
Genetica. 2013 Jun;141(4-6):189-93. doi: 10.1007/s10709-013-9717-6. Epub 2013 Apr 7.
Drosophila suzukii is a pest of small fruits in many parts of the world, whose management is limited to cultural practices and the use of insecticides. Here we describe a method to genetically manipulate this species in the first step to create female lethality strains useful for the sterile insect technique method of population suppression. This was achieved by the germ-line transformation of D. suzukii with a piggyBac transposon vector having a female-specific lethality effector construct. This can be used in a tetracycline-suppressible conditional gene expression system, when crossed to a suitable tet-transactivator strain. Transformation occurred efficiently, at a frequency of 16 % per fertile G0 embryo injected with vector and helper transposase plasmids. The vector was marked for transformant selection with the polyubiquitin-regulated EGFP fluorescent protein, and contains the attP landing site and heterospecific lox recombination sites for post-integration modification of the transgene vector. The 3xP3-AmCyan fluorescent protein marker was inserted within the lox sites to follow a possible recombinase-mediated cassette exchange, that would allow subsequent improvement of the transgenic strain by immobilization of the vector and introduction of new marker cassettes.
铃木果蝇是世界许多地区小型水果的害虫,其防治方法仅限于栽培措施和使用杀虫剂。在此,我们描述了一种对该物种进行基因操作的方法,第一步是创建对种群抑制的昆虫不育技术方法有用的雌性致死品系。这是通过用携带雌性特异性致死效应构建体的piggyBac转座子载体对铃木果蝇进行种系转化来实现的。当与合适的四环素反式激活菌株杂交时,该构建体可用于四环素可抑制的条件基因表达系统。转化效率很高,用载体和辅助转座酶质粒注射的每个可育G0胚胎的转化频率为16%。该载体用多聚泛素调节的EGFP荧光蛋白进行标记以选择转化体,并且包含用于转基因载体整合后修饰的attP着陆位点和异源lox重组位点。3xP3-AmCyan荧光蛋白标记插入lox位点内,以追踪可能的重组酶介导的盒式交换,这将允许通过固定载体和引入新的标记盒来随后改良转基因品系。