A novel PSEN2 p.Ser175Phe variant in a family with Alzheimer’s disease

• Published in: Neurological sciences Vol. 42; no. 6; pp. 2497 - 2504
• Main Authors: Guven, Gamze, Samanci, Bedia, Gulec, Cagri, Hanagasi, Hasmet, Gurvit, Hakan, Gokalp, Ebru Erzurumluoglu, Tepgec, Fatih, Guler, Suleyman, Uyguner, Oya, Bilgic, Basar
• Format: Journal Article
• Language: English
• Published: Cham Springer International Publishing 01-06-2021; Springer Nature B.V
• Subjects: Alzheimer's disease; Amyloid precursor protein; Apolipoprotein E; Dementia disorders; Genotypes; Medicine; Medicine & Public Health; Mutation; Neurodegenerative diseases; Neurology; Neuroradiology; Neurosciences; Neurosurgery; Original Article; Presenilin 1; Presenilin 2; Protein structure; Proteins; Psychiatry; Transcription; PSEN2; S175F; Alzheimer’s disease; novel
• ISSN: 1590-1874; 1590-3478
• DOI: 10.1007/s10072-021-05243-w

Alzheimer’s disease (AD) can be either sporadic or familial, and familial forms of AD accounts for only 5% of the cases. So far, autosomal dominantly inherited mutations in “
Presenilin 1
” (
PSEN1
), “
Presenilin 2
” (
PSEN2
), and “
Amyloid precursor protein
” (
APP
) genes were associated with familial AD. Amid the others, pathogenic mutations in the
PSEN2
gene are less common. In this study, we describe a novel heterozygous
PSEN2
(c.524C>T, p.Ser175Phe) alteration identified in a 58-year-old Turkish patient from a family with multiple dementia cases. This variant was further present in the patient’s clinically affected maternal cousin as well as in the asymptomatic mother and two maternal aunts who were carriers of the APOE ε2/ε3 genotype. The variant is located in the conserved residue of transmembrane domain III encoded by exon 6 of the major transcript. In silico protein structure analyses predicted that this variant might change the architecture of interaction between the two alpha helixes of PSEN2. We propose that p.Ser175Phe may have a pathogenic effect on protein function and may play a significant role in the molecular pathways leading to Alzheimer’s disease in this family.