• 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 120 and 146 amino acids Glu and Met of mouse PSEN1 was mutated as Lys and Leu in B-Psen1*M146L*E120K mice.
• mRNA expression analysis: Mouse Psen1 mRNA was detectable in wild-type C57BL/6JNifdc mice and homozygous B-Psen1*M146L*E120K mice. Sequence assays showed the homozygous B-Psen1*M146L*E120K mice consists of G to A point mutation at amino acid 120 and A to C point mutation at amino acid 146.
• Application: This product is used for pharmacodynamics and safety evaluation of Alzheimer’s disease (AD).

Gene targeting strategy for B-Psen1*P117L mice. The 120 and 146 amino acids Glu and Met of mouse Psen1 was mutated as Lys and Leu in B-Psen1*M146L*E120K mice.

Psen1 mRNA expression in wild-type C57BL/6J mice and homozygous B-Psen1*M146L*E120K mice by RT-PCR. Brain RNA were isolated from wild-type C57BL/6J mice (+/+) and homozygous B-Psen1*M146L*E120K mice (Mut/Mut), 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 mutations were confirmed via Sanger Sequencing.

Western blot analysis of PSEN1 protein expression in homozygous B-Psen1*M146L*E120K mice. Cortex and hippocampus lysates were collected from wild-type C57BL/6J mice (+/+) and homozygous B-Psen1*M146L*E120K mice (Mut/Mut), and then analyzed by western blot with anti-PSEN1 antibody (CST, #5643). 40 μg total proteins were loaded for western blotting analysis. PSEN1 was detected in cortex and hippocampus both in wild-type and homozygous B-Psen1*M146L*E120K mice.