Abstract
Deletion of the promoter and the first exon of the DNA polymerase beta gene (pol beta) in the mouse germ line results in a lethal phenotype. With the use of the bacteriophage-derived, site-specific recombinase Cre in a transgenic approach, the same mutation can be selectively introduced into a particular cellular compartment-in this case, T cells. The impact of the mutation on those cells can then be analyzed because the mutant animals are viable.
Publication types
-
Research Support, Non-U.S. Gov't
MeSH terms
-
Animals
-
DNA Nucleotidyltransferases / genetics
-
DNA Nucleotidyltransferases / metabolism
-
DNA Polymerase I / genetics*
-
DNA Polymerase I / metabolism
-
Female
-
Gene Deletion*
-
Genetic Engineering / methods*
-
Homozygote
-
Integrases*
-
Male
-
Mice
-
Mice, Knockout
-
Mice, Transgenic
-
Mutation
-
Recombination, Genetic
-
Stem Cells / enzymology
-
T-Lymphocytes / enzymology*
-
Transfection
-
Viral Proteins*
Substances
-
Viral Proteins
-
Cre recombinase
-
DNA Nucleotidyltransferases
-
Integrases
-
DNA Polymerase I