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Sci Rep. 2017 Mar 7;7:43331. doi: 10.1038/srep43331.

Efficient and rapid generation of large genomic variants in rats and mice using CRISMERE.

Author information

1
PHENOMIN, Institut Clinique de la Souris (ICS), CNRS, INSERM, University of Strasbourg, 1 rue Laurent Fries, F-67404 Illkirch-Graffenstaden, France.
2
Institut de Génétique et de Biologie Moléculaire et Cellulaire, Illkirch, France.
3
Centre National de la Recherche Scientifique, UMR7104, Illkirch, France.
4
Institut National de la Santé et de la Recherche Médicale, U964, Illkirch, France.
5
Université de Strasbourg, Illkirch, France.

Abstract

Modelling Down syndrome (DS) in mouse has been crucial for the understanding of the disease and the evaluation of therapeutic targets. Nevertheless, the modelling so far has been limited to the mouse and, even in this model, generating duplication of genomic regions has been labour intensive and time consuming. We developed the CRISpr MEdiated REarrangement (CRISMERE) strategy, which takes advantage of the CRISPR/Cas9 system, to generate most of the desired rearrangements from a single experiment at much lower expenses and in less than 9 months. Deletions, duplications, and inversions of genomic regions as large as 24.4 Mb in rat and mouse founders were observed and germ line transmission was confirmed for fragment as large as 3.6 Mb. Interestingly we have been able to recover duplicated regions from founders in which we only detected deletions. CRISMERE is even more powerful than anticipated it allows the scientific community to manipulate the rodent and probably other genomes in a fast and efficient manner which was not possible before.

PMID:
28266534
PMCID:
PMC5339700
DOI:
10.1038/srep43331
[Indexed for MEDLINE]
Free PMC Article

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