B-Psen1*P117L mice
| Strain Name |
C57BL/6JNifdc-Psen1tm1Bcgen/Bcgen
|
Common Name | B-Psen1*P117L mice |
| Background | C57BL/6JNifdc | Catalog number | 113061 |
|
Aliases |
AD3, FAD, PS1, PS-1, S182, CMD1U, PSNL1, ACNINV3 |
||
|
NCBI Gene ID |
5663 | ||
Model validation
Description
mRNA expression analysis
Protein expression analysis
- Mutations in the PSEN1 gene, encoding presenilin-1 (PS1), are the most common cause of familial Alzheimer’s disease (FAD).
- Alzheimer’s disease (AD) is characterized by the extracellular buildup of β-amyloid (Aβ) plaques and the intracellular aggregation of neurofibrillary tangles (NFTs), which are composed of hyperphosphorylated tau.
- APP is sequentially proteolytically cleaved by β- and γ-secretase, neurotoxic Aβ peptides are released, which can accumulate into oligomer aggregate. PSEN1 genes encode the major component of y-secretase, which is responsible for sequential proteolytic cleavages of amyloid precursor proteins and the subsequent formation of amyloid-β peptides. Mutations in the PSEN1 increase the production of Aβ peptide.
- In addition to amyloid precursor protein (APP) cleavage, PSEN1 can also affect other processes, such as Notch signaling, β-cadherin processing, and calcium metabolism.
- Gene editing strategy: The 117 amino acid Pro of mouse Psen1 was mutated as Leu in B-Psen1*P117L mice.
- mRNA expression analysis: Mouse Psen1 mRNA was detectable in wild-type C57BL/6JNifdc mice and homozygous B-Psen1*P117L mice. Sequence assays showed the homozygous B-Psen1*P117L mice consists of a C to T point mutation at amino acid 117.
- Application: This product is used for pharmacodynamics and safety evaluation of Alzheimer’s disease (AD).
Targeting strategy
Gene targeting strategy for B-Psen1*P117L mice. The 117 amino acid Pro of mouse Psen1 was mutated as Leu in B-Psen1*P117L mice.
Psen1 mRNA expression in wild-type C57BL/6J mice and homozygous B-Psen1*P117L mice by RT-PCR. Brain RNA were isolated from wild-type C57BL/6J mice (+/+) and homozygous B-Psen1*P117L mice (Mut/Mut), and then cDNA libraries were synthesized by reverse transcription, followed by PCR with mouse Psen1 primers. Mouse Psen1 mRNA was detectable in wild-type C57BL/6J and homozygous mice, and the point mutation was confirmed via Sanger Sequencing.
Western blot analysis of PSEN1 protein expression in homozygous B-Psen1*P117L mice. Cortex and hippocampus lysates were collected from wild-type C57BL/6J mice (+/+) and homozygous B-Psen1*P117L mice (Mut/Mut), and then analyzed by western blot with anti-PSEN1 antibody (CST, #5643). 40 μg of proteins were loaded for Western blot analysis. PSEN1 was detected in cortex and hippocampus both in wild-type and homozygous B-Psen1*P117L mice.
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