4.6 Article

Regulation of HLA class I expression by non-coding gene variations

Journal

PLOS GENETICS
Volume 18, Issue 6, Pages -

Publisher

PUBLIC LIBRARY SCIENCE
DOI: 10.1371/journal.pgen.1010212

Keywords

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Funding

  1. Swiss National Science Foundation [310030_173237/1]
  2. Swiss National Science Foundation (SNF) [310030_173237] Funding Source: Swiss National Science Foundation (SNF)

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This study investigates the allelic expression of the HLA class I loci and its association with non-coding gene variations. The researchers found that HLA-B alleles have the highest expression levels, followed by HLA-C and HLA-A alleles. They also observed coordinated expression of both alleles of the same locus and identified expression quantitative trait loci (eQTLs) that explain a significant portion of the variance in HLA expression. These eQTLs have larger effect sizes in stimulated cells compared to unstimulated cells. The findings suggest that non-coding gene variations may play a role in regulating HLA expression.
The Human Leukocyte Antigen (HLA) is a critical genetic system for different outcomes after solid organ and hematopoietic cell transplantation. Its polymorphism is usually determined by molecular technologies at the DNA level. A potential role of HLA allelic expression remains under investigation in the context of the allogenic immune response between donors and recipients. In this study, we quantified the allelic expression of all three HLA class I loci (HLA-A, B and C) by RNA sequencing and conducted an analysis of expression quantitative traits loci (eQTL) to investigate whether HLA expression regulation could be associated with non-coding gene variations. HLA-B alleles exhibited the highest expression levels followed by HLA-C and HLA-A alleles. The max fold expression variation was observed for HLA-C alleles. The expression of HLA class I loci of distinct individuals demonstrated a coordinated and paired expression of both alleles of the same locus. Expression of conserved HLA-A similar to B similar to C haplotypes differed in distinct PBMC's suggesting an individual regulated expression of both HLA class I alleles and haplotypes. Cytokines TNF alpha/IFN beta, which induced a very similar upregulation of HLA class I RNA and cell surface expression across alleles did not modify the individually coordinated expression at the three HLA class I loci. By identifying cis eQTLs for the HLA class I genes, we show that the non-coding eQTLs explain 29%, 13%, and 31% of the respective HLA-A, B, C expression variance in unstimulated cells, and 9%, 23%, and 50% of the variance in cytokine-stimulated cells. The eQTLs have significantly higher effect sizes in stimulated cells compared to unstimulated cells for HLA-B and HLA-C genes expression. Our data also suggest that the identified eQTLs are independent from the coding variation which defines HLA alleles and thus may be influential on intra-allele expression variability although they might not represent the causal eQTLs.

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