Liver regulatory mechanisms of noncoding variants at lipid and metabolic trait loci

HGG Adv. 2024 Apr 11;5(2):100275. doi: 10.1016/j.xhgg.2024.100275. Epub 2024 Jan 30.

Abstract

Genome-wide association studies (GWASs) have identified hundreds of risk loci for liver disease and lipid-related metabolic traits, although identifying their target genes and molecular mechanisms remains challenging. We predicted target genes at GWAS signals by integrating them with molecular quantitative trait loci for liver gene expression (eQTL) and liver chromatin accessibility QTL (caQTL). We predicted specific regulatory caQTL variants at four GWAS signals located near EFHD1, LITAF, ZNF329, and GPR180. Using transcriptional reporter assays, we determined that caQTL variants rs13395911, rs11644920, rs34003091, and rs9556404 exhibit allelic differences in regulatory activity. We also performed a protein binding assay for rs13395911 and found that FOXA2 differentially interacts with the alleles of rs13395911. For variants rs13395911 and rs11644920 in putative enhancer regulatory elements, we used CRISPRi to demonstrate that repression of the enhancers altered the expression of the predicted target and/or nearby genes. Repression of the element at rs13395911 reduced the expression of EFHD1, and repression of the element at rs11644920 reduced the expression of LITAF, SNN, and TXNDC11. Finally, we showed that EFHD1 is a metabolically active gene in HepG2 cells. Together, these results provide key steps to connect genetic variants with cellular mechanisms and help elucidate the causes of liver disease.

Keywords: CRISPR-interference; EFHD1; caQTL; cholesterol metabolism; chromatin accessibility; eQTL; genome-wide association studies; hepatocyte; liver; quantitative trait loci.

MeSH terms

  • Carrier Proteins
  • Genome-Wide Association Study*
  • Humans
  • Lipids
  • Liver Diseases*
  • Regulatory Sequences, Nucleic Acid

Substances

  • Lipids
  • TXNDC11 protein, human
  • Carrier Proteins