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Perinatal lethality ( ple): A mutation caused by integration of a transgene into distal mouse chromosome 15
Ist Teil von
Genomics (San Diego, Calif.), 1989-05, Vol.4 (4), p.498-504
Ort / Verlag
United States: Elsevier Inc
Erscheinungsjahr
1989
Quelle
Elsevier Journal Backfiles on ScienceDirect (DFG Nationallizenzen)
Beschreibungen/Notizen
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
trans
genic
perinatal
lethality (
Tg.ple).