Molecular and phenotypic characterization of a new mouse insertional mutation that causes a defect in the distal vertebrae of the spine

Genetics. 1995 Jul;140(3):1061-7. doi: 10.1093/genetics/140.3.1061.

Abstract

We have identified and characterized the phenotype of a new insertional mutation in one line of transgenic mice. Mice carrying this mutation, which we have designated TgN(Imusd)370Rpw, display undulations of the vertebrae giving rise to a novel kinky-tail phenotype. Molecular characterization of the insertion site indicates that the transgene integration has occurred without any substantial alterations in the structure of the host sequences. Using probes that flank the insertion site, we have mapped the mutation to chromosome 5 near the semidominant mutation, thick tail (Tht). Thick tail does not complement the TgN(Imusd)370Rpw mutation; compound mutants containing one copy of each mutation display a more severe phenotype than either mutation individually.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Actins / biosynthesis
  • Aging
  • Animals
  • Animals, Newborn
  • Base Sequence
  • Chloramphenicol O-Acetyltransferase / biosynthesis
  • Cloning, Molecular
  • Crosses, Genetic
  • Female
  • Homozygote
  • Liver / metabolism
  • Male
  • Mice
  • Mice, Transgenic
  • Molecular Sequence Data
  • Mutagenesis, Insertional*
  • Phenotype
  • Recombination, Genetic
  • Restriction Mapping
  • Spine / abnormalities*
  • Spine / growth & development

Substances

  • Actins
  • Chloramphenicol O-Acetyltransferase