Abstract
Mutations were targeted to the Hprt locus in murine embryonic stem cells by using sequence replacement vectors. When the vector was designed such that the mutated sequences were flanked on both sides by several kilobases of DNA homologous to the target locus, replacement of chromosomal sequences with the exogenous DNA occurred with precision. If, on the other hand, the target-homologous DNA on one arm of the vector was reduced to below 1 kb in length, the fidelity of recombination was diminished.
MeSH Terms
Animals
Drug Resistance
Gene Rearrangement/genetics
Genetic Vectors/genetics
Gentamicins/pharmacology
Mice
Mutagenesis, Site-Directed/genetics
Recombination, Genetic/genetics
Selection, Genetic
Stem Cells/metabolism
Thioguanine/pharmacology
Transformation, Genetic
Chemicals
Gentamicins
antibiotic G 418
Thioguanine
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Thomas K R
HHMI Research Laboratories, Eccles Institute of Human Genetics, University of Utah Medical Center, Salt Lake City 84112.
Deng C
Capecchi M R
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