Thoraval P, Afanassieff M, Cosset F L, Lasserre F, Verdier G, Coudert F, Dambrine G
Laboratoire de Virologie et d'Oncologie Aviaire, INRA, Nouzilly, France.
Transgenic Res. 1995 Nov;4(6):369-77. doi: 10.1007/BF01973755.
We have used vectors derived from avian leukosis viruses to transduce exogenous genes into early somatic stem cells of chicken embryos. The ecotropic helper cell line, Isolde, was used to generate stocks of NL-B vector carrying the Neo(r) selectable marker and the Escherichia coli lacZ gene. Microinjection of the NL-B vector directly beneath unincubated chicken embryo blastoderms resulted in infection of germline stem cells. One of the 16 male birds hatched (6.25%) from the injected embryos contained vector DNA sequences in its semen. Vector sequences were transmitted to G1 progeny at a frequency of 2.7%. Neo(r) and lacZ genes were transcribed in vitro in chicken embryo fibroblast cultures from transgenic embryos of the G2 progeny.
我们已使用源自禽白血病病毒的载体,将外源基因转导至鸡胚的早期体干细胞中。亲嗜性辅助细胞系Isolde用于制备携带新霉素抗性(Neo(r))选择标记和大肠杆菌lacZ基因的NL - B载体储备液。将NL - B载体显微注射到未孵化的鸡胚胚盘下方,可导致生殖系干细胞感染。从注射后的胚胎中孵出的16只雄性雏鸡中有1只(6.25%)精液中含有载体DNA序列。载体序列以2.7%的频率传递给G1代子代。Neo(r)和lacZ基因在来自G2代子代转基因胚胎的鸡胚成纤维细胞培养物中进行体外转录。