Mispairing C57BL/6 substrains of genetically engineered mice and wild-type controls can lead to confounding results as it did in studies of JNK2 in acetaminophen and concanavalin A liver injury

Chem Res Toxicol. 2011 Jun 20;24(6):794-6. doi: 10.1021/tx200143x. Epub 2011 May 24.

Abstract

C57BL/6 mice are widely used in biomedical research for the background of genetically engineered mice (GEM) and wild-type controls with the belief that the genetic background of GEM and control mice differ significantly by only one or more altered genes. This principle, however, does have limitations due in part to the existence of multiple substrains of C57BL/6 mice that should not be used interchangeably as they can differ both genetically and phenotypically. We show here that these mispairings do occur frequently and can lead to inaccurate and conflicting findings.

Publication types

  • Research Support, N.I.H., Intramural

MeSH terms

  • Acetaminophen / toxicity*
  • Analgesics, Non-Narcotic / toxicity*
  • Animals
  • Chemical and Drug Induced Liver Injury / enzymology*
  • Chemical and Drug Induced Liver Injury / genetics
  • Chemical and Drug Induced Liver Injury / pathology
  • Concanavalin A / toxicity*
  • Gene Knockdown Techniques
  • Genotype
  • Mice
  • Mice, Inbred C57BL / genetics*
  • Mice, Knockout
  • Mice, Transgenic / genetics*
  • Mitogen-Activated Protein Kinase 9 / genetics*
  • Mitogens / toxicity*

Substances

  • Analgesics, Non-Narcotic
  • Mitogens
  • Concanavalin A
  • Acetaminophen
  • Mitogen-Activated Protein Kinase 9