Department of Pathology, University of Michigan, Ann Arbor, MI 48109, USA.
Biochem J. 2012 Apr 15;443(2):355-9. doi: 10.1042/BJ20120249.
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.
最近的一项研究表明,源自 129 品系小鼠的胚胎干细胞(ES)系在半胱天冬酶 11 基因(Casp4)基因座内携带一个失活突变[Kayagaki、Warming、Lamkanfi、Vande Walle、Louie、Dong、Newton、Qu、Liu、Heldens、Zhang、Lee、 Roose-Girma 和 Dixit(2011)《自然》479,117-121]。因此,如果使用 129 ES 细胞来靶向与半胱天冬酶 11 紧密连锁的基因,那么由此产生的小鼠也可能携带半胱天冬酶 11 缺陷作为乘客突变。在本研究中,我们检查了在 129 ES 细胞中生成的紧密连锁的 c-IAP(细胞凋亡抑制剂)基因的靶向小鼠的遗传基因座,尽管它们已经进行了广泛的回交以使其背景为 C57BL/6,但 c-IAP1(-/-)动物也缺乏半胱天冬酶 11。因此,应该在这个新的背景下重新评估从这些小鼠中获得的数据。