Single-cell RNA sequencing of peripheral blood links cell-type-specific regulation of splicing to autoimmune and inflammatory diseases

Nat Genet. 2024 Dec;56(12):2739-2752. doi: 10.1038/s41588-024-02019-8. Epub 2024 Dec 3.

Abstract

Alternative splicing contributes to complex traits, but whether this differs in trait-relevant cell types across diverse genetic ancestries is unclear. Here we describe cell-type-specific, sex-biased and ancestry-biased alternative splicing in ~1 M peripheral blood mononuclear cells from 474 healthy donors from the Asian Immune Diversity Atlas. We identify widespread sex-biased and ancestry-biased differential splicing, most of which is cell-type-specific. We identify 11,577 independent cis-splicing quantitative trait loci (sQTLs), 607 trans-sGenes and 107 dynamic sQTLs. Colocalization between cis-eQTLs and trans-sQTLs revealed a cell-type-specific regulatory relationship between HNRNPLL and PTPRC. We observed an enrichment of cis-sQTL effects in autoimmune and inflammatory disease heritability. Specifically, we functionally validated an Asian-specific sQTL disrupting the 5' splice site of TCHP exon 4 that putatively modulates the risk of Graves' disease in East Asian populations. Our work highlights the impact of ancestral diversity on splicing and provides a roadmap to dissect its role in complex diseases at single-cell resolution.

MeSH terms

  • Alternative Splicing* / genetics
  • Asian People / genetics
  • Autoimmune Diseases* / genetics
  • Female
  • Genetic Predisposition to Disease
  • Graves Disease / genetics
  • Humans
  • Inflammation / genetics
  • Leukocyte Common Antigens / genetics
  • Leukocytes, Mononuclear* / metabolism
  • Male
  • Quantitative Trait Loci*
  • Sequence Analysis, RNA
  • Single-Cell Analysis*

Substances

  • PTPRC protein, human
  • Leukocyte Common Antigens