Applying gene-editing technology to elucidate the functional consequence of genetic and epigenetic variation in Alzheimer's disease

被引:8
|
作者
Schrauben, Michael [1 ]
Dempster, Emma [1 ]
Lunnon, Katie [1 ]
机构
[1] Exeter Univ, Univ Exeter, Sch Med, Exeter, Devon, England
关键词
Alzheimer's disease (AD); CRISPR; epigenetics; genetics; genome editing; MOUSE MODELS; CRISPR-CAS9; SYSTEM; APOLIPOPROTEIN-E; DNA METHYLATION; HUMAN GENOME; RNA; RISK; ACTIVATION; MECHANISMS; GENERATION;
D O I
10.1111/bpa.12881
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Recent studies have highlighted a potential role of genetic and epigenetic variation in the development of Alzheimer's disease. Application of the CRISPR-Cas genome-editing platform has enabled investigation of the functional impact that Alzheimer's disease-associated gene mutations have on gene expression. Moreover, recent advances in the technology have led to the generation of CRISPR-Cas-based tools that allow for high-throughput interrogation of different risk variants to elucidate the interplay between genomic regulatory features, epigenetic modifications, and chromatin structure. In this review, we examine the various iterations of the CRISPR-Cas system and their potential application for exploring the complex interactions and disruptions in gene regulatory circuits that contribute to Alzheimer's disease.
引用
收藏
页码:992 / 1004
页数:13
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