Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.
Nat Methods December 1, 2005; 2 (12): 975-9.
Show Gene links Show Anatomy links

Transgenic Xenopus laevis embryos can be generated using phiC31 integrase.

Bacteriophage phiC31 encodes an integrase that can mediate the insertion of extrachromosomal DNA into genomic DNA. Here we show that the coinjection of mRNA encoding phiC31 integrase with plasmid DNA encoding the green fluorescent protein (GFP) can be used to generate transgenic X. laevis embryos. Despite integration into the genome, appropriate promoter expression required modification of the reporter plasmid by bracketing the GFP reporter gene with tandem copies of the chicken beta-globin 5'' HS4 insulator to relieve silencing owing to chromatin position effects. These experiments demonstrate that the integration of insulated gene sequences using phiC31 integrase can be used to efficiently create transgenic embryos in X. laevis and may increase the practical use of phiC31 integrase in other systems as well.

PubMed ID: 16299484
PMC ID: PMC3552317
Article link: Nat Methods
Grant support: [+]

Species referenced: Xenopus laevis
Genes referenced: hbg1

References [+] :
Bell, Stopped at the border: boundaries and insulators. 1999, Pubmed