rdf:type |
|
lifeskim:mentions |
umls-concept:C0008633,
umls-concept:C0017262,
umls-concept:C0026882,
umls-concept:C0185117,
umls-concept:C0205145,
umls-concept:C0524637,
umls-concept:C0678640,
umls-concept:C1521840,
umls-concept:C1524063,
umls-concept:C1704788,
umls-concept:C1705150,
umls-concept:C1708726,
umls-concept:C2347567,
umls-concept:C2911684
|
pubmed:issue |
43
|
pubmed:dateCreated |
1994-12-1
|
pubmed:abstractText |
Using the FLP/FRT system for site-specific recombination and the wild-type recognition site (FRT) in conjunction with certain mutant FRT sites, it becomes possible to provoke, with high yield, a double-reciprocal crossover event in cultured mammalian cells. It is demonstrated that this technology enables a targeting of expression cassettes to appropriate chromosomal reference sites in the recipient cell to improve the concepts of reverse genetics. The design of mutant FRT sites promoting such a process will be delineated. Our results show that the five spacer mutations tested are functional as the wild type but differ in the extent of their cross-recombination, which has to be minimized for their simultaneous usage.
|
pubmed:language |
eng
|
pubmed:journal |
|
pubmed:citationSubset |
IM
|
pubmed:chemical |
|
pubmed:status |
MEDLINE
|
pubmed:month |
Nov
|
pubmed:issn |
0006-2960
|
pubmed:author |
|
pubmed:issnType |
Print
|
pubmed:day |
1
|
pubmed:volume |
33
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
12746-51
|
pubmed:dateRevised |
2006-11-15
|
pubmed:meshHeading |
pubmed-meshheading:7947678-Animals,
pubmed-meshheading:7947678-Base Sequence,
pubmed-meshheading:7947678-Binding Sites,
pubmed-meshheading:7947678-Cell Line,
pubmed-meshheading:7947678-Cricetinae,
pubmed-meshheading:7947678-DNA,
pubmed-meshheading:7947678-DNA Nucleotidyltransferases,
pubmed-meshheading:7947678-Kidney,
pubmed-meshheading:7947678-Molecular Sequence Data,
pubmed-meshheading:7947678-Mutagenesis,
pubmed-meshheading:7947678-Mutation,
pubmed-meshheading:7947678-Polymerase Chain Reaction,
pubmed-meshheading:7947678-Recombination, Genetic,
pubmed-meshheading:7947678-Repetitive Sequences, Nucleic Acid,
pubmed-meshheading:7947678-Transfection,
pubmed-meshheading:7947678-Transferases,
pubmed-meshheading:7947678-beta-Galactosidase
|
pubmed:year |
1994
|
pubmed:articleTitle |
Use of mutated FLP recognition target (FRT) sites for the exchange of expression cassettes at defined chromosomal loci.
|
pubmed:affiliation |
GBF, Gesellschaft für Biotechnologische Forschung mbH, Braunschweig-Stöckheim, Germany.
|
pubmed:publicationType |
Journal Article
|