Transgenic mice produced by intracytoplasmic sperm injection.
- Author:
Ming LI
1
;
A-Yong YAN
;
Hui YAO
;
Xiao-Rong AN
;
Ke-Mian GOU
Author Information
1. Stated Key Laboratories for Agrobiotechnologies, College of Biological Sciences, China Agricultural University, Beijing.
- Publication Type:Journal Article
- MeSH:
Animals;
Male;
Mice;
Mice, Inbred C57BL;
Mice, Inbred DBA;
Mice, Transgenic;
genetics;
Sperm Injections, Intracytoplasmic;
methods
- From:
Chinese Journal of Biotechnology
2006;22(5):784-788
- CountryChina
- Language:Chinese
-
Abstract:
In our previous study, normal and fertile mice were successful produced from oocytes following intracytoplasmic sperm injection (ICSI). In the present study, the possibility of producing transgenic embryos and offspring with this procedure was evaluated. After freezing-thawed once using HEPES-CZB medium without cryoprotectants, the cauda sperm from KM fertile male were exposed to the circular or linear pEGFP-N1 DNA for 1 min and then co-injected into metaphase II oocytes of B6D2F1 strain. When the zygotes with two pronuclei were cultured in CZB medium to day 3.5, 39.1% (9/23) of them, derived from oocytes co-injected with sperm head and pEGFP-N1 plasmid DNA, were expressed GFP protein. After transfer of the ICSI embryos with two pronuclei from co-injection of sperm head and foreign DNA, seven recipients delivered 30 pups (23.8%, 30/126). Southern blot results revealed that three of sixteen offspring integrated with GFP and neomycin genes together (18.8 %). Interestingly, all of them were produced from oocytes co-injected sperm head and linear DNA (33.3%, 3/9), while none of seven ICSI offspring integrated either GFP or neomycin gene in the group of co-injection of sperm head and circular plasmid DNA. These results indicated that the high efficiency of transgenic mouse could be produced by ICSI. It may be shown that linear DNA is more easily to integrate into host genome than circular DNA when ICSI was used to produce transgenic animals.
