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Allele : Tg(APPswe,PSEN1dE9)85Dbo transgene insertion 85, David R Borchelt

Primary Identifier  MGI:3524957 Allele Type  Transgenic
Attribute String  Humanized sequence, Inserted expressed sequence Gene  Tg(APPswe,PSEN1dE9)85Dbo
Strain of Origin  (C57BL/6 x C3H)F2 Is Recombinase  false
Is Wild Type  false
description  Mice carrying this double transgene develop beta-amyloid deposits in the brain by 6 to 7 months of age.
molecularNote  Two transgenes inserted at a single locus in Chromosome 9 between Arpp21 and Pdcd6ip. Each transgene is controlled by the mouse prion promoter and contains a cDNA sequence. In one transgene the cDNA encodes a chimeric amyloid beta (A4) precursor protein (APPswe). In the second transgene the cDNA encodes the "DeltaE9" mutation of human presenilin 1. The DeltaE9 mutation of the human presenilin 1 gene is a deletion of exon 9 and corresponds to a form of early-onset Alzheimer's disease. The amyloid beta precursor protein coding sequences were altered by replacing mouse sequence encoding three amino acids of the A-beta domain with the human coding sequence for these residues. The chimeric amyloid beta (A4) precursor protein sequence was then further modified to encode the Swedish mutations K595N/M596L found in human. Both the transgenic peptide and holoprotein are detected by Signet Laboratories' monoclonal 6E10 antibody, which is specific for human sequence within this region. Human presenilin protein, which in high levels displaces detectable endogenous mouse protein, is immunodetected in the double transgenic mouse in whole brain protein homogenates. Human amyloid precursor protein is also immunodetected in these mice in whole brain protein homogenates. Transgene insertion occurred on Chr 9, causing a 1 bp duplication.
  • mutations:
  • Duplication,
  • Insertion
  • synonyms:
  • APP/PS1,
  • APPswe/PS1dE9,
  • APPswe/PS1deltaE9,
  • APPswe/PS1deltaE9,
  • Mo/Hu APPswe PS1dE9,
  • APPswe/PS1dE9,
  • APdE9,
  • 2xTg Ad,
  • APP-PS1,
  • 2xTg Ad,
  • APP/PS1,
  • APdE9,
  • APP-PS1,
  • Mo/Hu APPswe PS1dE9
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1 Feature

Genome

2 Expresses

0 Mutation Involves

Phenotype

Mouse alleles --> Mammalian phenotypes (MP terms)

 

Other

11 Carried By

0 Driven By

1000 Publication categories