LIU Qin,ZHANG Jin-yu,WANG Lu-lu,LIU Chang-e,WANG Yong,WAN Ying.Production of EGFP transgenic mice by lentiviral transgenesis[J].J Amry Med Univ (J Third Mil Med Univ),2008,30(10):885-889.
LIU Qin,ZHANG Jin-yu,WANG Lu-lu,LIU Chang-e,WANG Yong,WAN Ying.Production of EGFP transgenic mice by lentiviral transgenesis[J].J Amry Med Univ (J Third Mil Med Univ),2008,30(10):885-889.DOI:
Production of EGFP transgenic mice by lentiviral transgenesis
Objective To establish an efficient and reliable method for transgenic mouse production
we performed lentiviral vector-mediated transgenesis in mice. Methods The leniviral vector FUGW was packaged by co-transfection of 293FT cells with two packaging vectors
psPAX2
and pMD2.G. The two packaging vectors provide structural proteins and envelope protein respectively which are necessary for the proper package of pseudotype virus. The tire of the pseudotype virus was tested by FACS after infecting 293FT cells with the solution containing the virus particles. The virus was concentrated by high speed centrifugation
and concentrated virus solution was injected into perivitelline space of mouse 1-cell eggs. EGFP expression in pre-implantation eggs was observed under fluorescent microscope
and that in mouse body under UV light. Results The titre of the primary virus solution was ≥10
6
TU/ml
and that after concentration was ≥10
9
TU/ml. The concentrated virus solution efficiently infected mouse eggs after injected into the perivitelline space. On 60
84
132 h after injection
EGFP expression was observed in the injected eggs. At 24 h after injection when the majority of the injected eggs was in 2-cell stage
more than 90% of the eggs was EGFP positive under fluorescent microscope. The injected 2-cell eggs was transferred into the oviduct of pseudo-pregnant female mice
and 42.9% (12/28) of the transferred mice became pregnant. The pregnant recipient mice gave birth to 120 pups
of which 60.8% (73/120) showed visible EGFP expression under UV light. The overall transgenic mouse production efficiency (transgenic mouse/injected eggs) was 5.0% (73/1 453). The EGFP transgenic founder mice were mated with wild-type mice
and EGFP expression was detected in F1
F2 and F3 offspring
indicating that the EGFP expression can be transmitted through germline cells. Conclusion Lentiviral transgenesis is an efficient and reliable method to produce transgenic mice. We have established the technological system for lentiviral transgenesis in mice.