Tg(Eno2-Glrb)456Wha
Transgene Detail
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Symbol: |
Tg(Eno2-Glrb)456Wha |
Name: |
transgene insertion 456, Hans Weiher |
MGI ID: |
MGI:5086014 |
Synonyms: |
rat GlyR beta transgene, TG456, Tg(NSE-Glrb)456 |
Transgene: |
Tg(Eno2-Glrb)456Wha Location: unknown
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Alliance: |
Tg(Eno2-Glrb)456Wha page
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Strain of Origin: |
(C57BL/6 x DBA/2)F1 x DBA/2
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Transgene Type: |
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Transgenic (Inserted expressed sequence) |
Mutation: |
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Insertion
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Tg(Eno2-Glrb)456Wha expresses
1 gene
Transgene expresses:
Organism |
Expressed Gene |
Homolog in Mouse |
Note |
rat |
Glrb (25456) |
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Mutation details: The transgene contains the promoter of the rat enolase 2, gamma neuronal gene driving expression of a cDNA encoding the beta subunit of the rat glycine receptor, which is followed by the SV40 small T-antigen splice and polyadenylation signals. . Brains of both heterozygous and homozygous transgenic mice of line 456 on a homozygous Glrbspa background contain Glrb mRNA and membrane-bound glycine receptor alpha-1 subunit (a proxy for the beta receptor subunit), analyzed via mRNA northern and western blot analysis, respectively, at levels not significantly different from those in non-transgenic Glrbspa homozygotes. Despite this, binding of strychnine to spinal cord membrane preparations from the homozygous transgenic mice is consistently higher than to preps from the non-transgenic animals, though still quite low.
(J:32212, J:60037)
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Inheritance: |
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Recessive |
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View phenotypes and curated references for all genotypes (concatenated display).
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Mouse strains and cell lines
available from the International Mouse Strain Resource
(IMSR) |
Carrying this Mutation: |
Mouse Strains: 0 strains available
Cell Lines: 0 lines available
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This is one of four transgenic founder lines that were derived ( J:32212). Despite the very low expression of the transgene, when homozygous it rescues the reproductive and much of the neurologic phenotype of Glrb spa/ Glrb spa mice ( J:60037).
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Original: |
J:32212 Hartenstein B, et al., Low level expression of glycine receptor beta subunit transgene is sufficient for phenotype correction in spastic mice. EMBO J. 1996 Mar 15;15(6):1275-82 |
All: |
2 reference(s) |
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