FB2024_04 , released June 25, 2024
Human Disease Model Report: Alzheimer disease 4
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General Information
Name
Alzheimer disease 4
FlyBase ID
FBhh0000121
Disease Ontology Term
Parent Disease
Overview

This report describes Alzheimer disease 4 (AD4), which is a subtype of Alzheimer disease; AD3 exhibits an autosomal dominant pattern of inheritance. The human gene implicated in this disease is PSEN2 (Presenilin 2), the catalytic component of a gamma-secretase complex. Gamma-secretase is responsible for proteolytic cleavage of amyloid precursor protein (APP) and NOTCH receptor proteins. PSEN2 is also implicated in dilated cardiomyopathy 1V (CMD1V, FBhh0000155). There is a single fly ortholog of PSEN2, Dmel\Psn, for which classical hypomorphic alleles, RNAi-targeting constructs, and alleles caused by insertional mutagenesis have been generated. Dmel\Psn is also orthologous to the human gene PSEN1 (see report for AD3, FBhh0000120).

Multiple different UAS constructs of the human gene Hsap\PSEN2 have been introduced into flies, including wild-type PSEN2 and genes carrying mutational lesions implicated in AD4. Variant(s) implicated in human disease (as transgenic human gene, PSEN2): M239V and N141I variant forms of the human gene have been introduced into flies, but have not been characterized to date.

For data concerning disease models using the fly Psn gene, see the report for 'Alzheimer disease, presenilin-related' (FBhh0000623).

[updated Aug. 2019 by FlyBase; FBrf0222196]

Disease Summary Information
Parent Disease Summary: Alzheimer disease
Symptoms and phenotype

Alzheimer disease (AD) is the most common form of progressive dementia in the elderly. [from MIM:104300; 2016.01.08]

Memory loss is the most common sign of Alzheimer disease. As the disorder progresses, some people with AD experience personality and behavioral changes; other common symptoms include agitation, restlessness, withdrawal, and loss of language skills. Total care is usually required during the advanced stages of the disease. Affected individuals usually survive 8 to 10 years after the appearance of symptoms, but the course of the disease can range from 1 to 25 years. Death usually results from pneumonia, malnutrition, or general body wasting. [from Genetics Home Reference, Alzheimer disease; 2016.01.08]

Alzheimer disease can be classified as early-onset or late-onset. The signs and symptoms of the early-onset form appear before age 65, while the late-onset form appears after age 65. The early-onset form is much less common than the late-onset form, accounting for less than 5 percent of all cases of Alzheimer disease. [from Genetics Home Reference, Alzheimer disease; 2016.01.08]

Specific Disease Summary: Alzheimer disease 4
OMIM report

[ALZHEIMER DISEASE 4; AD4](https://omim.org/entry/606889)

Human gene(s) implicated

[PRESENILIN 2; PSEN2](https://omim.org/entry/600759)

Symptoms and phenotype

Alzheimer disease 4 (AD4) is characterized by typical symptoms of Alzheimer disease (described above).

Genetics

Alzheimer disease 4 is inherited as an autosomal dominant; it is associated with heterozygous mutations in the PSEN2 gene. [from MIM:606889; 2016.01.08]

Cellular phenotype and pathology

The PSEN2 gene encodes presenilin-2, which forms the catalytic component of a gamma-secretase complex. Gamma-secretase is responsible for proteolytic cleavage of amyloid precursor protein (APP) and NOTCH receptor proteins. Gamma-secretase is a multiprotein complex containing PSEN1 or PSEN2 and multiple other components. [from MIM:104311, MIM:600759; 2016.01.08]

Molecular information
External links
Disease synonyms
AD4
Alzheimer disease, early-onset
Alzheimer disease, familial, 4
early-onset familial Alzheimer disease
eFAD
EOFAD
Ortholog Information
Human gene(s) in FlyBase
Human gene (HGNC)
Symbol / Name
D. melanogaster ortholog (based on DIOPT)
Comments on ortholog(s)

Many to one: 2 human to 1 Drosophila. Two human genes, PSEN1 and PSEN2, are orthologous to the fly gene Dmel\Psn.

Other mammalian ortholog(s) used
    D. melanogaster Gene Information (1)
    Gene Groups / Pathways
    Comments on ortholog(s)

    Ortholog of human genes PSEN2 and PSEN1 (1 Drosophila to 2 human). Dmel\Psn shares 47-48% identity and 59-62% similarity with the 2 human genes.

    Orthologs and Alignments from DRSC
    DIOPT - DRSC Integrative Ortholog Prediction Tool - Click the link below to search for orthologs in Humans
    Other Genes Used: Viral, Bacterial, Synthetic (0)
      Summary of Physical Interactions (8 groups)
      protein-protein
      Interacting group
      Assay
      References
      ubiquitin reconstruction
      anti tag coimmunoprecipitation, anti tag western blot, western blot, anti bait coimmunoprecipitation
      proximity ligation assay, fluorescence microscopy
      anti tag coimmunoprecipitation, anti tag western blot
      molecular sieving, western blot
      molecular sieving, western blot, anti tag coimmunoprecipitation
      anti tag coimmunoprecipitation, anti tag western blot
      pull down, anti tag western blot
      Alleles Reported to Model Human Disease (Disease Ontology) (26 alleles)
      Models Based on Experimental Evidence ( 21 )
      Allele
      Disease
      Evidence
      References
      Modifiers Based on Experimental Evidence ( 15 )
      Allele
      Disease
      Interaction
      References
      Alleles Representing Disease-Implicated Variants
      Genetic Tools, Stocks and Reagents
      Sources of Stocks
      Contact lab of origin for a reagent not available from a public stock center.
      Bloomington Stock Center Disease Page
      Related mammalian, viral, bacterial, or synthetic transgenes
      Allele
      Transgene
      Publicly Available Stocks
      Selected Drosophila transgenes
      Allele
      Transgene
      Publicly Available Stocks
      RNAi constructs available
      Allele
      Transgene
      Publicly Available Stocks
      Selected Drosophila classical alleles
      Allele
      Allele class
      Mutagen
      Publicly Available Stocks
      P-element activity
      CRISPR/Cas9
      CRISPR/Cas9
      ethyl methanesulfonate
      loss of function allele
      ethyl methanesulfonate
      loss of function allele
      ethyl methanesulfonate
      Delta2-3 transposase
      loss of function allele
      ethyl methanesulfonate
      P-element activity
      loss of function allele
      ethyl methanesulfonate
      Delta2-3 transposase
      loss of function allele
      ethyl methanesulfonate
      References (10)