Abstract
Chromosomal rearrangements are important resources for genetic studies. Recently, a Cre-loxP-based method to introduce defined chromosomal rearrangements (deletions, duplications, and inversions) into the mouse genome (chromosome engineering) has been established. To explore the limits of this technology systematically, we have evaluated this strategy on mouse chromosome 11. Although the efficiency of Cre-loxP-mediated recombination decreases with increasing genetic distance when the two endpoints are on the same chromosome, the efficiency is not limiting even when the genetic distance is maximized. Rearrangements encompassing up to three quarters of chromosome 11 have been constructed in mouse embryonic stem (ES) cells. While larger deletions may lead to ES cell lethality, smaller deletions can be produced very efficiently both in ES cells and in vivo in a tissue- or cell-type-specific manner. We conclude that any chromosomal rearrangement can be made in ES cells with the Cre-loxP strategy provided that it does not affect cell viability. In vivo chromosome engineering can be potentially used to achieve somatic losses of heterozygosity in creating mouse models of human cancers.
ACKNOWLEDGMENTS
We thank Sandra Rivera, Sukeshi Vaishnav, and Yin-Chai Cheah for technical assistance; Hong Su for an Hsd17b1 targeted cell line; Wei Wen Cai for the BAC clones used in FISH analysis; Michael Schneider for the αMyHC-Cre mouse line; Pentao Liu for helpful discussions; Patrick Biggs, Xiaozhong Wang, and Meredith Wentland for helpful comments on the manuscript; and Sylvia Perez for secretarial assistance.
This work is partially supported by grants from the National Institutes of Health, the National Cancer Institute, and DAMD17-98-1-8280. A.B. is an investigator with the Howard Hughes Medical Institute.