Literature DB >> 7841363

Early detection of mouse wobbler mutation: a model of pathological motoneurone death.

V des Portes1, M Coulpier, J Melki, P A Dreyfus.   

Abstract

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.

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Year:  1994        PMID: 7841363     DOI: 10.1097/00001756-199410000-00005

Source DB:  PubMed          Journal:  Neuroreport        ISSN: 0959-4965            Impact factor:   1.837


  3 in total

1.  A rat mutation producing demyelination (dmy) maps to chromosome 17.

Authors:  T Kuramoto; C Sotelo; N Yokoi; T Serikawa; E Goñalons Sintes; J Cantó Martorell; J L Guénet
Journal:  Mamm Genome       Date:  1996-12       Impact factor: 2.957

Review 2.  The wobbler mouse: a neurodegeneration jigsaw puzzle.

Authors:  Séverine Boillée; Marc Peschanski; Marie-Pierre Junier
Journal:  Mol Neurobiol       Date:  2003-08       Impact factor: 5.590

3.  Bcl-2 sensitivity differentiates two pathways for motoneuronal death in the wobbler mutant mouse.

Authors:  M Coulpier; M P Junier; M Peschanski; P A Dreyfus
Journal:  J Neurosci       Date:  1996-10-01       Impact factor: 6.167

  3 in total

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