Alzheimer's disease risk SNPs show no strong effect on miRNA expression in human lymphoblastoid cell lines

Neurobiol Aging. 2020 Feb:86:202.e1-202.e3. doi: 10.1016/j.neurobiolaging.2019.08.013. Epub 2019 Aug 20.

Abstract

The role of microRNAs (miRNAs) in the pathogenesis of Alzheimer's disease (AD) is currently extensively investigated. In this study, we assessed the potential impact of AD genetic risk variants on miRNA expression by performing large-scale bioinformatic data integration. Our analysis was based on genetic variants from 3 AD genome-wide association studies (GWASs). Association with miRNA expression was tested by expression quantitative trait locus analysis using next-generation miRNA sequencing data generated in lymphoblastoid cell lines. Although, overall, we did not identify a strong effect of AD GWAS variants on miRNA expression in this cell type, we highlight 2 notable outliers, that is, miR-29c-5p and miR-6840-5p. MiR-29c-5p was recently reported to be involved in the regulation of BACE1 and SORL1 expression. In conclusion, despite 2 exceptions, our large-scale assessment provides only limited support for the hypothesis that AD GWAS variants act as miRNA expression quantitative trait loci.

Keywords: Alzheimer's disease; GWAS; Gene expression; Genetic association; eQTLs; miRNA.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alzheimer Disease / genetics*
  • Amyloid Precursor Protein Secretases / genetics
  • Amyloid Precursor Protein Secretases / metabolism
  • Aspartic Acid Endopeptidases / genetics
  • Aspartic Acid Endopeptidases / metabolism
  • Cell Line
  • Gene Expression*
  • Genome-Wide Association Study
  • Humans
  • LDL-Receptor Related Proteins / genetics
  • LDL-Receptor Related Proteins / metabolism
  • Lymphocytes / metabolism*
  • Membrane Transport Proteins / genetics
  • Membrane Transport Proteins / metabolism
  • MicroRNAs / genetics*
  • MicroRNAs / metabolism*
  • Negative Results
  • Polymorphism, Single Nucleotide*
  • Quantitative Trait Loci / genetics
  • Risk

Substances

  • LDL-Receptor Related Proteins
  • Membrane Transport Proteins
  • MicroRNAs
  • SORL1 protein, human
  • Amyloid Precursor Protein Secretases
  • Aspartic Acid Endopeptidases
  • BACE1 protein, human