About the Knockout Mouse Project knockout strategies

The two groups funded to produce knockout alleles for the KOMP project use targeting constructs that have different and complementary properties. Below is a general outline of these constructs that may be helpful in your assessment of the preferred approach for targeting your gene(s) of interest.




Constructs used by Regeneron, Inc.

Regeneron, Inc. will use the following general construct for creating knockouts for KOMP. In most cases these will be complete null alleles that delete the entire protein coding sequence of the target gene. This allele design can be applied to any gene transcribed by RNA polymerase II regardless of its size, intron-exon structure, RNA splicing pattern, or protein-coding capacity.

Reference: Valenzuela, D. M., Murphy, A. J., Frendewey, D., Gale, N. W., Economides, A. N., Auerbach, W., Poueymirou, W. T., Adams, N. C., Rojas, J., Yasenchak, J., et al. (2003). High-throughput engineering of the mouse genome coupled with high-resolution expression analysis. Nat Biotechnol 21, 652-659.


Constructs used by the CSD (CHORI/Sanger/UC Davis) team

CSD: CHORI (Children's Hospital Oakland Research Institute), the Wellcome Trust Sanger Institute, and the University of California at Davis use promoterless and promoter-driven targeting cassettes for the generation of a 'Knockout-first allele' (Testa et al., 2004). This strategy relies on the identification of a 'critical' exon common to all transcript variants that, when deleted, creates a frame-shift mutation. The KO-first allele is flexible and can produce reporter knockouts, conditional knockouts, and null alleles following exposure to site-specific recombinases Cre and Flp. Because the target gene must contain a "critical" exon, the approach may not be readily ammenable for small genes with few exons.



Derivative alleles

tm1a: KO first allele (reporter-tagged insertion allele)

tm1b: post-Cre (reporter-tagged deletion alllele)

tm1c: post-Flp (conditional allele)

tm1d: post-Flp and Cre (deletion allele with no reporter)

tm1e: targeted, non-conditional allele

Reference

Testa G, Schaft J, van der Hoeven F, Glaser S, Anastassiadis K, Zhang Y, Hermann T, Stremmel W, Stewart AF. (2004). A reliable lacZ expression reporter cassette for multipurpose, knockout-first alleles. Genesis 38: 151-8.