Double knockouts. Production of mutant cell lines in cardiovascular research.
- 1 October 1993
- journal article
- review article
- Published by Wolters Kluwer Health in Hypertension
- Vol. 22 (4) , 646-651
- https://doi.org/10.1161/01.hyp.22.4.646
Abstract
Double knockouts by homologous recombination is a method for producing cell lines with an inactivating mutation in any desired gene. The biochemical analysis of genetically altered cell lines has been important in determining the function of specific proteins. Until recently, mutant cell lines have been produced by random mutagenesis and then selection for a particular phenotypic change. Recent technological advances in gene targeting by homologous recombination now enable the production of mutants in any desired gene. Diploid cells contain two copies or alleles of each gene encoded on an autosome (nonsex) chromosome. In most cases, both alleles must be inactivated to produce a phenotypic change in a mutant cell line, hence the term "double knockout." We and others have described the production of mutationally altered cell lines by inactivating both alleles by the production of two targeting vectors, two separate homologous recombination events, and selection. A simpler procedure, involving considerably less effort and time, has been used to inactivate several alpha-subunits of G proteins and other genes. This method facilitates the inactivation of more than one gene in a single cell line.Keywords
This publication has 17 references indexed in Scilit:
- Highly efficient gene targeting in embryonic stem cells through homologous recombination with isogenic DNA constructs.Proceedings of the National Academy of Sciences, 1992
- Manipulating the Genome by Homologous Recombination in Embryonic Stem CellsAnnual Review of Neuroscience, 1992
- Targeted inactivation of the insulin receptor gene in mouse 3T3-L1 fibroblasts via homologous recombination.Proceedings of the National Academy of Sciences, 1991
- Using Embryonic Stem Cells to Introduce Mutations into the Mouse Germ Line1Biology of Reproduction, 1991
- Homologous recombination at c-fyn locus of mouse embryonic stem cells with use of diphtheria toxin A-fragment gene in negative selection.Proceedings of the National Academy of Sciences, 1990
- Consecutive inactivation of both alleles of the pim-1 proto-oncogene by homologous recombination in embryonic stem cellsNature, 1990
- Gene targeting in murine embryonic stem cells: Introduction of specific alterations into the mammalian genomeGene Analysis Techniques, 1990
- A mutant neomycin phosphotransferase II gene reduces the resistance of transformants to antibiotic selection pressure.Proceedings of the National Academy of Sciences, 1990
- Disruption of the proto-oncogene int-2 in mouse embryo-derived stem cells: a general strategy for targeting mutations to non-selectable genesNature, 1988
- Genetic demonstration of mitotic recombination in cultured chinese hamster cell hybridsCell, 1984