A single vector containing modified cre recombinase and LOX recombination sequences for inducible tissue-specific amplification of gene expression
Author(s) -
S. J. Kaczmarczyk
Publication year - 2001
Publication title -
nucleic acids research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 9.008
H-Index - 537
eISSN - 1362-4954
pISSN - 0305-1048
DOI - 10.1093/nar/29.12.e56
Subject(s) - biology , vector (molecular biology) , recombination , cre recombinase , recombinase , genetics , flp frt recombination , gene , microbiology and biotechnology , gene duplication , gene expression , site specific recombination , recombinant dna , genetic recombination , transgene , genetically modified mouse
The selective alteration of the genome using Cre recombinase to target the rearrangement of genes flanked by LOX recognition sequences has required the use of two separate genetic constructs in trans, one containing cre and the other containing the gene of interest flanked by LOX sites. We have developed a strategy in which both the cre recombinase gene and LOX recombination sites may be cloned within a single vector in cis. This method uses a modified form of Cre (CREM) that contains alterations to the 5' region including the introduction of a Kozak consensus sequence and insertion of a functional intron. This system allows for the inducible, tissue-specific activation or inactivation of gene expression in a single vector and can be utilized for the 300-fold amplification of gene expression from a weak promoter. This approach can be applied to targeting strategies for generating genetically altered mice and gene therapy.
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