| Literature DB >> 11981557 |
Kevin Eggan1, Anja Rode, Isabell Jentsch, Caroline Samuel, Thomas Hennek, Hartmut Tintrup, Branko Zevnik, Jennifer Erwin, Janet Loring, Laurie Jackson-Grusby, Michael R Speicher, Ralf Kuehn, Rudolf Jaenisch.
Abstract
We have devised a general strategy for producing female mice from 39,X0 embryonic stem (ES) cells derived from male cell lines carrying a targeted mutation of interest. We show that the Y chromosome is lost in 2% of subclones from 40,XY ES cell lines, making the identification of targeted 39,X0 subclones a routine procedure. After gene targeting, male and female mice carrying the mutation can be generated by tetraploid embryo complementation from the 40,XY ES cell line and its 39,X0 derivatives. A single intercross then produces homozygous mutant offspring. Because this strategy avoids outcrossing and therefore segregation of mutant alleles introduced into the ES cells, the time and expense required for production of experimental mutant animals from a targeted ES cell clone are substantially reduced. Our data also indicate that ES cells have inherently unstable karyotypes, but this instability does not interfere with production of adult ES cell tetraploid mice.Entities:
Mesh:
Year: 2002 PMID: 11981557 DOI: 10.1038/nbt0502-455
Source DB: PubMed Journal: Nat Biotechnol ISSN: 1087-0156 Impact factor: 54.908