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Cell adhesion molecule pathway genes are regulated by cis-regulatory SNPs and show significantly altered expression in Alzheimer's disease brains

  • Xinjie Bao
  • , Gengfeng Liu
  • , Yongshuai Jiang
  • , Qinghua Jiang
  • , Mingzhi Liao
  • , Rennan Feng
  • , Liangcai Zhang
  • , Guoda Ma
  • , Shuyan Zhang
  • , Zugen Chen
  • , Bin Zhao
  • , Renzhi Wang
  • , Keshen Li*
  • , Guiyou Liu
  • *Corresponding author for this work
  • Chinese Academy of Medical Sciences
  • The First Hospital of Harbin
  • Harbin Medical University
  • School of Life Science and Technology, Harbin Institute of Technology
  • Rice University
  • Guangdong Medical College
  • University of California at Los Angeles
  • CAS - Tianjin Institute of Industrial Biotechnology

Research output: Contribution to journalArticlepeer-review

Abstract

We previously identified the cell adhesion molecule (CAM) pathway as a consistent signal in 2 Alzheimer's disease (AD) genome-wide association studies (GWAS). However, the genetic mechanisms of the CAM pathway in AD are unclear. Here, we conducted pathway analysis using (1) Kyoto Encyclopedia of Genes and Genomes and Gene Ontology pathways; (2) 4 brain expression GWAS datasets; and (3) 2 whole-genome AD case-control expression datasets. Using the 4 brain expression GWAS datasets, we identified that genes regulated by cis-regulatory single-nucleotide polymorphisms (SNPs) were significantly enriched in the CAM pathway (p = 2.05E-06, p = 6.10E-07, p = 2.05E-06, and p = 1.47E-07 for each dataset). Interestingly, CAM is a significantly enriched pathway using down-regulated genes (raw p = 0.0235 and adjusted p = 0.0305) and all differentially expressed genes (raw p = 0.0105 and adjusted p = 0.0156) in dataset 5, and all differentially expressed genes (raw p = 0.0041 and adjusted p = 0.0062) in dataset 6. Collectively, our results show that CAM pathway genes are regulated by cis-regulatory SNPs and show significantly altered expression in AD. We believe that our results advance the understanding of AD mechanisms and will be useful for future genetic studies of AD.

Original languageEnglish
Pages (from-to)2904.e1-2904.e7
JournalNeurobiology of Aging
Volume36
Issue number10
DOIs
StatePublished - 1 Oct 2015
Externally publishedYes

Keywords

  • Alzheimer's disease
  • Brain expression
  • Cell adhesion molecules
  • Genome-wide association studies
  • Pathway analysis

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