Pathogenicity: Alzheimer's Disease : Pathogenic
Clinical Phenotype: Alzheimer's Disease
Reference Assembly: GRCh37 (105)
Position: Chr14:73640279 A>G
dbSNP ID: rs63750450
Coding/Non-Coding: Coding
Mutation Type: Point, Missense
Codon Change: TAT to TGT
Reference Isoform: PSEN1 isoform 1 (467 aa)
Genomic Region: Exon 5


This mutation has been identified in muliple families and individuals worldwide suffering from familial early onset AD. Age of onset ranges from 33 to 54 years of age. 

It was first described in a Dutch family known as Family 1066, whose published pedigree included 10 affected family members over four generations. The clinical diagnosis of Alzheimer’s disease was pathologically confirmed in at least three members of the family. The mean age at onset was 42 years (range: 39 to 49 years). Disease in this family previously had been linked to chromosome 14 (van Duijn et al., 1994). The mutation segregated with disease in this family and was transmitted in an autosomal-dominant manner (Cruts et al., 1998).

The mutation was subsequently detected in one individual during a genetic screen of patients with AD; no further clinical details were reported (Rogaeva et al., 2001).

Another family, known as Family 372, was reported with five affected family members over three generations. The mean age of onset in this family was 48 years (range: 36 to 54 years). No postmortem confirmation of the diagnosis was available at the time of the report (Janssen et al., 2003).

This mutation was also detected in an individual with early onset Alzheimer’s disease, which was confirmed by autopsy. The proband experienced symptom onset at age 43 and died at age 52. The proband’s mother also had early onset dementia (onset at age 33; death at age 42) (unpublished findings, personal communication, T.D. Bird; 2014).

This mutation was reported in an additional kindred. Consistent with the previously reported families, the proband experienced symptom onset in her 40s. She died in her 50s with pathologically confirmed AD. She had a family history of dementia; her mother had experienced a similar disease course. The mutation was also detected in the proband’s daughter, who was asymptomatic at the time (Doran et al., 2006, meeting abstract).

The Y115C mutation was also found in a large French study reporting on 56 families affected by putatively familial early onset Alzheimer disease (Wallon et al., 2012). The Y115C mutation was detected in one proband (family EXT 238). DNA from two affected family members was not available, so segregation with disease could not be determined. Age of onset in this family was reported as 39 to 40 years of age, with a duration of three years.

Additional Y115C carriers with familial early onset AD have been reported in France (Lanoiselee et al., 2017) and Korea (Park et al., 2020). 


Postmortem examination revealed pathology consistent with AD in Family 1066 (van Duijn et al., 1994). In addition, the Korean individual was amyloid-positive as assessed by FMM-PET imaging, and MRI revealed atrophy in the bilateral medial temporal areas, while FDG-PET showed hypometabolism in bilateral temporoparietal areas (Park et al., 2020). Moreover, in one French individual, cerebrospinal fluid biomarkers, including Aβ42, tau, and phospho-tau, were consistent with AD (Lanoiselee et al., 2017).

Biological Effect

HEK-293 cells transfected with mutant PSEN1 secreted significantly more Aβ42 (approximately 5.4-fold) than cells expressing wild-type PSEN1. The Aβ42:Aβ40 ratio was also increased (De Jonghe et al., 1999). An in vitro assay using purified proteins to test the ability of this mutant to cleave the APP-C99 substrate also revealed an increased Aβ42/Aβ40 ratio (>15-fold). However, in this case, the alteration was due to a dramatic reduction in Aβ40 production, accompanied by a moderate decrease in Aβ42 production (Sun et al., 2017).

Moreover, as assessed in cortical neurons derived from patient induced pluripotent stem cells, Y115C disrupts lysosome function and autophagy, leading to impaired lysosomal proteolysis and defective autophagosome clearance. These effects appear to be caused by accumulation of β-C-terminal fragments of APP (Hung and Livesey, 2018).

In silico algorithms predicted the mutation to be probably damaging (Polyphen2) and damaging (SIFT) (Park et al., 2020). Based on the pathogenicity criteria developed by Guerreiro and colleagues (Guerreiro et al., 2010), this mutation was classified as definitely pathogenic (Lanoiselée et al., 2017).

Research Models

Induced pluripotent stem cell lines have been created from patient fibroblasts (Moore et al., 2015).

Last Updated: 17 Mar 2020


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Paper Citations

  1. . A population-based study of familial Alzheimer disease: linkage to chromosomes 14, 19, and 21. Am J Hum Genet. 1994 Oct;55(4):714-27. PubMed.
  2. . Estimation of the genetic contribution of presenilin-1 and -2 mutations in a population-based study of presenile Alzheimer disease. Hum Mol Genet. 1998 Jan;7(1):43-51. PubMed.
  3. . Screening for PS1 mutations in a referral-based series of AD cases: 21 novel mutations. Neurology. 2001 Aug 28;57(4):621-5. PubMed.
  4. . Early onset familial Alzheimer's disease: Mutation frequency in 31 families. Neurology. 2003 Jan 28;60(2):235-9. PubMed.
  5. Abstracts of the Sixteenth Meeting of the European Neurological Society. May 27-31, 2006. Lausanne, Switzerland. J Neurol. 2006 May;253 Suppl 2:II3-159. PubMed.
  6. . The French series of autosomal dominant early onset Alzheimer's disease cases: mutation spectrum and cerebrospinal fluid biomarkers. J Alzheimers Dis. 2012 Jan 1;30(4):847-56. PubMed.
  7. . APP, PSEN1, and PSEN2 mutations in early-onset Alzheimer disease: A genetic screening study of familial and sporadic cases. PLoS Med. 2017 Mar;14(3):e1002270. Epub 2017 Mar 28 PubMed.
  8. . Analysis of dementia-related gene variants in APOE ε4 noncarrying Korean patients with early-onset Alzheimer's disease. Neurobiol Aging. 2020 Jan;85:155.e5-155.e8. Epub 2019 May 22 PubMed.
  9. . Aberrant splicing in the presenilin-1 intron 4 mutation causes presenile Alzheimer's disease by increased Abeta42 secretion. Hum Mol Genet. 1999 Aug;8(8):1529-40. PubMed.
  10. . Analysis of 138 pathogenic mutations in presenilin-1 on the in vitro production of Aβ42 and Aβ40 peptides by γ-secretase. Proc Natl Acad Sci U S A. 2017 Jan 24;114(4):E476-E485. Epub 2016 Dec 5 PubMed.
  11. . Altered γ-Secretase Processing of APP Disrupts Lysosome and Autophagosome Function in Monogenic Alzheimer's Disease. Cell Rep. 2018 Dec 26;25(13):3647-3660.e2. PubMed.
  12. . Genetic screening of Alzheimer's disease genes in Iberian and African samples yields novel mutations in presenilins and APP. Neurobiol Aging. 2010 May;31(5):725-31. Epub 2008 Jul 30 PubMed.
  13. . APP metabolism regulates tau proteostasis in human cerebral cortex neurons. Cell Rep. 2015 May 5;11(5):689-96. Epub 2015 Apr 23 PubMed.

Further Reading

Protein Diagram

Primary Papers

  1. . Estimation of the genetic contribution of presenilin-1 and -2 mutations in a population-based study of presenile Alzheimer disease. Hum Mol Genet. 1998 Jan;7(1):43-51. PubMed.

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