Tg(Thy1-GLRA1*R271Q)382Wha
Transgene Detail

Summary

• Symbol: Tg(Thy1-GLRA1*R271Q)382Wha
• Name: transgene insertion 382, Hans Weiher
• MGI ID: MGI:5306914
• Synonyms: tg271Q-382, Tg(Thy1-Glra1*R271Q)382Wha
• Transgene: Tg(Thy1-GLRA1*R271Q)382Wha Location: unknown
• Alliance: Tg(Thy1-GLRA1*R271Q)382Wha page

Transgene origin

• Strain of Origin: (C57BL/6 X DBA/2)F1 x C57BL/6

Transgene description

• Transgene Type: Transgenic (Humanized sequence, Inserted expressed sequence)
• Mutation: Insertion
• Tg(Thy1-GLRA1*R271Q)382Wha expresses 1 gene
  Transgene expresses:
  

  Organism

  Expressed Gene

  Homolog in Mouse

  Note

  human

  GLRA1 (2741)

  Glra1

  (MGI:95747)

• Mutation details: This transgene contains a cDNA encoding a mutant human glycine receptor alpha 1 subunit in which the arginine at amino acid position 271 has been replaced by glutamine (R271Q); this mutation is associated with a dominant hereditary hyperekplexia (human startle disease). The human cDNA has replaced, in an expression vector, a segment of the mouse thymus antigen 1 gene whose deletion limits expression to neurons. Reverse transcription-polymerase chain reaction (RT-PCR) analysis using primers that amplify both mouse and human Glra1/GLRA1 cDNA demonstrates elevated mRNA expression in the spinal cord and forebrain of transgenic versus wild-type mice. In situ hybridization analysis confirms higher expression in transgenic brains and reveals sites of ectopic expression. Expression in mice of this line is significantly lower (roughly 50%) than in mice bearing Tg(Thy1-GLRA1*R271Q)300Wha. While competition between endogenous and transgene-derived alpha 1 receptor subunits for endogenous beta subunits confounds quantitative ligand-binding analysis, presence of complete receptors at sites of ectopic GLRA1 mRNA expression in transgenic, but not wild-type, brains is shown by competitive and non-competitive ligand binding to frozen brain sections. (J:76009)
• Inheritance: Recessive

Disease models

Find Mice (IMSR)

• 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

References

• Original: J:76009 Becker L, et al., Disease-specific human glycine receptor alpha1 subunit causes hyperekplexia phenotype and impaired glycine- and GABA(A)-receptor transmission in transgenic mice. J Neurosci. 2002 Apr 1;22(7):2505-12
• All: 1 reference(s)