| Literature DB >> 18953339 |
Christian Frøkjaer-Jensen1, M Wayne Davis, Christopher E Hopkins, Blake J Newman, Jason M Thummel, Søren-Peter Olesen, Morten Grunnet, Erik M Jorgensen.
Abstract
At present, transgenes in Caenorhabditis elegans are generated by injecting DNA into the germline. The DNA assembles into a semistable extrachromosomal array composed of many copies of injected DNA. These transgenes are typically overexpressed in somatic cells and silenced in the germline. We have developed a method that inserts a single copy of a transgene into a defined site. Mobilization of a Mos1 transposon generates a double-strand break in noncoding DNA. The break is repaired by copying DNA from an extrachromosomal template into the chromosomal site. Homozygous single-copy insertions can be obtained in less than 2 weeks by injecting approximately 20 worms. We have successfully inserted transgenes as long as 9 kb and verified that single copies are inserted at the targeted site. Single-copy transgenes are expressed at endogenous levels and can be expressed in the female and male germlines.Entities:
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Year: 2008 PMID: 18953339 PMCID: PMC2749959 DOI: 10.1038/ng.248
Source DB: PubMed Journal: Nat Genet ISSN: 1061-4036 Impact factor: 38.330