Perinatal lethality (ple): a mutation caused by integration of a transgene into distal mouse chromosome 15

D R Beier, C C Morton, A Leder, R Wallace, P Leder

Research output: Contribution to journalArticlepeer-review

Abstract

We have used cytogenetic and recombinational analysis to determine the position of a transgene integrated into the mouse genome. The transgene maps to band F on the physical map of mouse chromosome 15 by in situ analysis and is tightly linked genetically to a cluster of loci that include the mutations caracul (Ca) and microcytic anemia (mk). Genetic analysis of the offspring of noninbred animals carrying the transgene and marker loci demonstrates a significant deficiency of homozygous progeny at weaning. When inbred mice heterozygous for the transgene are mated, about one-quarter of their offspring are homozygous; none of these animals survives more than 1 day after birth. It appears likely that a recessive insertional mutation has occurred as a result of transgene integration into a locus required for postnatal viability. We call this mutation transgenic perinatal lethality (Tg.ple).

Original languageEnglish
Pages (from-to)498-504
Number of pages7
JournalGenomics
Volume4
Issue number4
Publication statusPublished - May 1989

Keywords

  • Animals
  • Chromosome Mapping
  • Genes, Lethal
  • Genes, Recessive
  • Genes, Synthetic
  • Mice
  • Mice, Inbred Strains
  • Mice, Transgenic
  • Mutation
  • Nucleic Acid Hybridization
  • Oncogenes
  • Recombination, Genetic
  • Journal Article
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

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