Rapid genotyping of newborn gene mutant mice

J Neurosci Methods. 2000 Jul 31;100(1-2):123-6. doi: 10.1016/s0165-0270(00)00241-7.

Abstract

One important aspect of utilizing transgenic mice is the need to genotype them in order to distinguish mice that carry a disrupted gene or a transgene from mice that do not. Current methods for genotyping include isolation of genomic DNA from tail biopsies followed by PCR amplification. Particularly, both digestion of tail tissue using proteinase K as well as resuspension of purified DNA are time-consuming and were usually carried out overnight. Here, we describe a rapid and robust method for the genotyping of bdnf targeted mice which allows us to determine the genotype of newborn mice at the day of birth within 6 h. After a freezing-thawing step tail tissue is digested in less than 2 h, and the DNA is precipitated, resuspended and ready for PCR in about 60 min. The method could be easily adapted to a variety of different mutant mice and especially should benefit neuroscientists interested in using animals with known genotype very early in postnatal development.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Animals, Newborn / genetics*
  • Brain-Derived Neurotrophic Factor / deficiency
  • Brain-Derived Neurotrophic Factor / genetics
  • DNA Mutational Analysis / methods*
  • Genetic Testing / methods*
  • Genotype*
  • Mice
  • Mice, Knockout / genetics*
  • Polymerase Chain Reaction
  • Time Factors

Substances

  • Brain-Derived Neurotrophic Factor