Title:Integrated Genomic Analysis Revealed Associated Genes for Alzheimer’s Disease in APOE4 Non-Carriers
Volume: 16
Issue: 8
Author(s): Shan Jiang, Chun-Yun Zhang, Ling Tang, Lan-Xue Zhao, Hong-Zhuan Chen*Yu Qiu*
Affiliation:
- Institute of Interdisciplinary Integrative Biomedical Research, Shanghai University of Traditional Chinese Medicine, Shanghai 201210,China
- Department of Pharmacology and Chemical Biology, Institute of Medical Sciences, Shanghai Jiao Tong University School of Medicine, Shanghai 200025,China
Keywords:
late-onset Alzheimer's disease, APOE4, APOE4 non-carriers, integrated genomic analysis, protein kinase Cγ, tau
phosphorylation.
Abstract:
Background: APOE4 is the strongest genetic risk factor for late-onset Alzheimer’s disease
(LOAD). LOAD patients carrying or not carrying APOE4 manifest distinct clinico-pathological characteristics.
APOE4 has been shown to play a critical role in the pathogenesis of AD by affecting various
aspects of pathological processes. However, the pathogenesis involved in LOAD not-carrying APOE4
remains elusive.
Objective: We aimed to identify the associated genes involved in LOAD not-carrying APOE4.
Methods: An integrated genomic analysis of datasets of genome-wide association study, genome-wide
expression profiling and genome-wide linkage scan and protein–protein interaction network construction
were applied to identify associated gene clusters in APOE4 non-carriers. The role of one of hub gene of
an APOE4 non-carrier-associated gene cluster in tau phosphorylation was studied by knockdown and
western blot.
Results: We identified 12 gene clusters associated with AD APOE4 non-carriers. The hub genes associated
with AD in these clusters were MAPK8, POU2F1, XRCC1, PRKCG, EXOC6, VAMP4, SIRT1,
MME, NOS1, ABCA1 and LDLR. The associated genes for APOE4 non-carriers were enriched in hereditary
disorder, neurological disease and psychological disorders. Moreover, knockdown of PRKCG to
reduce the expression of protein kinase Cγ isoform enhanced tau phosphorylation at Thr181 and Thr231
and the expression of glycogen synthase kinase 3β and cyclin-dependent kinase 5 in the presence of
APOE3 but not APOE4.
Conclusion: The study provides new insight into the mechanism of distinct pathogenesis of LOAD not
carrying APOE4 and prompts the functional exploration of identified genes based on APOE genotypes.
