A recent study revealed that ES (embryonic stem) cell lines derived from the 129 murine strain carry an inactivating mutation within the caspase 11 gene (Casp4) locus [Kayagaki, Warming, Lamkanfi, VandeWalle, Louie, Dong, Newton, Qu, Liu, Heldens, Zhang, Lee, Roose-Girma and Dixit (2011) Nature 479, 117-121]. Thus, if 129 ES cells are used to target genes closely linked to caspase 11, the resulting mice might also carry the caspase 11 deficiency as a passenger mutation. In the present study, we examined the genetic loci of mice targeted for the closely linked c-IAP (cellular inhibitor of apoptosis) genes, which were generated in 129 ES cells, and found that, despite extensive backcrossing into a C57BL/6 background, c-IAP1 -/- animals are also deficient in caspase 11. Consequently, data obtained from these mice should be re-evaluated in this new context. © 2012 The Author(s).
CITATION STYLE
Kenneth, N. S., Younger, J. M., Hughes, E. D., Marcotte, D., Barker, P. A., Saunders, T. L., & Duckett, C. S. (2012). An inactivating caspase 11 passenger mutation originating from the 129 murine strain in mice targeted for c-IAP1. Biochemical Journal, 443(2), 355–359. https://doi.org/10.1042/BJ20120249
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