Identification of a novel mutation in the presenilin 1 gene in a Chinese Alzheimer's disease family.

Abstract

This study has identified a gene mutation in a Chinese family with Alzheimer's disease (AD). Family members were screened by a set of medical examinations and neuropsychological tests. Their DNA was extracted from blood cells and sequenced for gene mutation in the amyloid precursor protein (APP), the presenilin 1 (PS1) and the presenilin 2 (PS2) genes. Genetic analysis showed that the AD patients in the family harbored a T to G missense mutation at the position 314 in exon 4 of the PS1 gene, resulting in a change of F105C in amino acid sequence. Clinical manifestation of these patients included memory loss, counting difficulty, personality change, disorientation, dyscalculia, agnosia, aphasia, and apraxia, which was similar to that of the familial AD (FAD) patients harboring other PS1 mutations. We intend to add a novel mutation F105C of the PS1 gene to the pool of FAD mutations. With the current available genetic data, mutations of the PS1 gene account for the majority of gene mutations in Chinese FAD.

• Authors: Bo Deng, Yan Lian, Xin Wang, Fan Zeng, Bin Jiao, Ye-Ran Wang, Chun-Rong Liang, Yu-Hui Liu, Xian-Le Bu, Xiu-Qing Yao, Chi Zhu, Lu Shen, Hua-Dong Zhou, Tao Zhang, Yan-Jiang Wang
• Journal: Neurotoxicity research (Neurotox Res) Vol. 26 Issue 3 Pg. 211-5 (Oct 2014) ISSN: 1476-3524 [Electronic] United States
• PMID: 24737487 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)

Chemical References

• PSEN1 protein, human
• Presenilin-1

Topics

• Alzheimer Disease (genetics, pathology, psychology)
• Asian People
• Brain (pathology)
• Family
• Female
• Humans
• Male
• Middle Aged
• Mutation, Missense
• Neuropsychological Tests
• Pedigree
• Presenilin-1 (genetics)