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An inactivating caspase 11 passenger mutation originating from the 129 murine strain in mice targeted for c-IAP1.

Niall S Kenneth | J Michael Younger | Elizabeth D Hughes | Danielle Marcotte | Philip A Barker | Thomas L Saunders | Colin S Duckett
The Biochemical journal | 2012

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, Vande Walle, 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.

Pubmed ID: 22332634

Research resources used in this publication

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Associated grants

  • Agency: NCI NIH HHS, United States
    Id: R01 CA142809
  • Agency: NHLBI NIH HHS, United States
    Id: T32 HL007517

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Novus Biologicals (tool)

RRID:SCR_004286

Commercial antibody vendor which supplies antibodies and other products to life science researchers.

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FVB/NJ (tool)

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Mus musculus with name FVB/NJ from IMSR.

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C57BL/6J (tool)

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