Uncovering the epigenetic regulatory clues of PRRT1 in Alzheimer's disease: a strategy integrating multi-omics analysis with explainable machine learning

Alzheimers Res Ther. 2025 Jan 7;17(1):12. doi: 10.1186/s13195-024-01646-x.

Abstract

Background: Alzheimer's disease (AD) is a complex neurodegenerative disorder with a largely unexplored epigenetic landscape.

Objective: This study employs an innovative approach that integrates multi-omics analysis and explainable machine learning to explore the epigenetic regulatory mechanisms underlying the epigenetic signature of PRRT1 implicated in AD.

Methods: Through comprehensive DNA methylation and transcriptomic profiling, we identified distinct epigenetic signatures associated with gene PRRT1 expression in AD patient samples compared to healthy controls. Utilizing interpretable machine learning models and ELMAR analysis, we dissected the complex relationships between these epigenetic signatures and gene expression patterns, revealing novel regulatory elements and pathways. Finally, the epigenetic mechanisms of these genes were investigated experimentally.

Results: This study identified ten epigenetic signatures, constructed an interpretable AD diagnostic model, and utilized various bioinformatics methods to create an epigenomic map. Subsequently, the ELMAR R package was used to integrate multi-omics data and identify the upstream transcription factor MAZ for PRRT1. Finally, experiments confirmed the interaction between MAZ and PRRT1, which mediated apoptosis and autophagy in AD.

Conclusion: This study adopts a strategy that integrates bioinformatics analysis with molecular experiments, providing new insights into the epigenetic regulatory mechanisms of PRRT1 in AD and demonstrating the importance of explainable machine learning in elucidating complex disease mechanisms.

Keywords: Alzheimer's disease; Biomarker; Epigenetic; Interpretable machine learning; Multi-omics analysis.

MeSH terms

  • Alzheimer Disease* / genetics
  • Computational Biology / methods
  • DNA Methylation* / genetics
  • Epigenesis, Genetic* / genetics
  • Epigenomics / methods
  • Female
  • Gene Expression Profiling / methods
  • Humans
  • Machine Learning*
  • Male
  • Multiomics
  • Nerve Tissue Proteins* / genetics

Substances

  • Nerve Tissue Proteins