A transcriptome-wide Mendelian randomization study to uncover tissue-dependent regulatory mechanisms across the human phenome

Nat Commun. 2020 Jan 10;11(1):185. doi: 10.1038/s41467-019-13921-9.

Abstract

Developing insight into tissue-specific transcriptional mechanisms can help improve our understanding of how genetic variants exert their effects on complex traits and disease. In this study, we apply the principles of Mendelian randomization to systematically evaluate transcriptome-wide associations between gene expression (across 48 different tissue types) and 395 complex traits. Our findings indicate that variants which influence gene expression levels in multiple tissues are more likely to influence multiple complex traits. Moreover, detailed investigations of our results highlight tissue-specific associations, drug validation opportunities, insight into the likely causal pathways for trait-associated variants and also implicate putative associations at loci yet to be implicated in disease susceptibility. Similar evaluations can be conducted at http://mrcieu.mrsoftware.org/Tissue_MR_atlas/.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aromatase / genetics
  • Fibrillin-2 / genetics
  • Gene Expression Regulation
  • Genetic Association Studies
  • Genetic Predisposition to Disease
  • Genetic Variation
  • Humans
  • Hydroxymethylglutaryl CoA Reductases / genetics
  • Mendelian Randomization Analysis*
  • Multifactorial Inheritance
  • Phenomics*
  • Phenotype
  • Polymorphism, Single Nucleotide
  • Quantitative Trait Loci
  • Ribosomal Proteins / genetics
  • Thyroid Diseases / genetics
  • Thyroid Diseases / metabolism
  • Transcriptome*

Substances

  • FBN2 protein, human
  • Fibrillin-2
  • RPS26 protein, human
  • Ribosomal Proteins
  • HMGCR protein, human
  • Hydroxymethylglutaryl CoA Reductases
  • Aromatase
  • CYP19A1 protein, human