EARLY DETECTION OF MOUSE WOBBLER MUTATION - A MODEL OF PATHOLOGICAL MOTONEURON DEATH

被引:16
作者
DESPORTES, V
COULPIER, M
MELKI, J
DREYFUS, PA
机构
[1] INSERM,U153,F-75005 PARIS,FRANCE
[2] HOP NECKER ENFANTS MALAD,F-75743 PARIS 15,FRANCE
关键词
MOUSE NEUROLOGICAL MUTANTS; MOTOR NEURON DISEASE; WOBBLER; ANIMAL MODELS; SPINAL MUSCULAR ATROPHY; LINKAGE; GENETICS; CHROMOSOME MAPPING; OLIGONUCLEOTIDE PROBES;
D O I
10.1097/00001756-199410000-00005
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
THE mouse recessive mutation wobbler, carried by the C57BL/6J strain, is a naturally occurring model of motoneurone death. The gene is unknown and in the absence of predictive markers, mutants have to be diagnosed by phenotypic criteria at 4 weeks after birth. We localized the wobbler gene to chromosome 11 at 0.98 +/- 1.1 cM from the glutamine synthetase (Glns) gene. A polymorphic allele of the Glns gene was then introduced into the congenic wobbler strain by intraspecific crossing. One-quarter of the offspring expressed the same phenotypic mutation as true wobbler and were detectable by PCR, as they are homozygous for the wobbler-linked Glns allele. The new mutants exhibit motoneurone degeneration despite the new genetic background.
引用
收藏
页码:1861 / 1864
页数:4
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