A Novel Heterozygous Missense Variant in the CIAO1 Gene in a Family with Alzheimer’s Disease: The Val67Ile Variant Promotes the Interaction of CIAO1 and Amyloid-β Protein Precursor

Author:

Nan Haitian1,Kim Yeon-Jeong2,Tsuchiya Mai1,Fukao Toko1,Hara Noriko3,Hagihara Atsushi3,Nishioka Kenya4,Hattori Nobutaka4,Hara Norikazu5,Ikeuchi Takeshi5,Ohtsuka Toshihisa2,Takiyama Yoshihisa1

Affiliation:

1. Department of Neurology, Graduate School of Medical Sciences, University of Yamanashi, Yamanashi, Japan

2. Department of Biochemistry, Graduate School of Medical Sciences, University of Yamanashi, Yamanashi, Japan

3. Department of Internal Medicine, Minobusan Hospital, Yamanashi, Japan

4. Department of Neurology, Juntendo University School of Medicine, Tokyo, Japan

5. Department of Molecular Genetics, Brain Research Institute, Niigata University, Niigata, Japan

Abstract

Familial dementia is a rare inherited disease involving progressive impairment of memory, thinking, and behavior. We report a novel heterozygous pathogenic variant (c.199G > A, p.Val67Ile) in the CIAO1 gene that appears to be co-segregated with Alzheimer’s disease in a Japanese family. Biochemical analysis of CIAO1 protein revealed that the variant increases the interaction of CIAO1 with immature amyloid-β protein precursor (AβPP), but not mature or soluble AβPP, indicating plausible CIAO1 involvement in AβPP processing. Our study indicates that a heterozygous variant in the CIAO1 gene may be closely related to autosomal dominant familial dementia.

Publisher

IOS Press

Subject

Psychiatry and Mental health,Geriatrics and Gerontology,Clinical Psychology,General Medicine,General Neuroscience

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