Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2010 Mar;69(3):611-7.
doi: 10.1136/ard.2009.118315. Epub 2009 Oct 23.

Association of IRF5 polymorphisms with activation of the interferon alpha pathway

Ornella J Rullo  1 , Jennifer M P Woo, Hui Wu, Alice D C Hoftman, Paul Maranian, Brittany A Brahn, Deborah McCurdy, Rita M Cantor, Betty P Tsao
Affiliations

Association of IRF5 polymorphisms with activation of the interferon alpha pathway

Ornella J Rullo et al. Ann Rheum Dis. 2010 Mar.

Abstract

Objective: The genetic association of interferon regulatory factor 5 (IRF5) with systemic lupus erythematosus (SLE) susceptibility has been convincingly established. To gain understanding of the effect of IRF5 variation in individuals without SLE, a study was undertaken to examine whether such genetic variation predisposes to activation of the interferon alpha (IFNalpha) pathway.

Methods: Using a computer simulated approach, 14 single nucleotide polymorphisms (SNPs) and haplotypes of IRF5 were tested for association with mRNA expression levels of IRF5, IFNalpha and IFN-inducible genes and chemokines in lymphoblastoid cell lines (LCLs) from individuals of European (CEU), Han Chinese (CHB), Japanese (JPT) and Yoruba Nigerian (YRI) backgrounds. IFN-inducible gene expression was assessed in LCLs from children with SLE in the presence and absence of IFNalpha stimulation.

Results: The major alleles of IRF5 rs13242262 and rs2280714 were associated with increased IRF5 mRNA expression levels in the CEU, CHB+JPT and YRI samples. The minor allele of IRF5 rs10488631 was associated with increased IRF5, IFNalpha and IFN-inducible chemokine expression in CEU (p(c)=0.0005, 0.01 and 0.04, respectively). A haplotype containing these risk alleles of rs13242262, rs10488631 and rs2280714 was associated with increased IRF5, IFNalpha and IFN-inducible chemokine expression in CEU LCLs. In vitro studies showed specific activation of IFN-inducible genes in LCLs by IFNalpha.

Conclusions: SNPs of IRF5 in healthy individuals of a number of ethnic groups were associated with increased mRNA expression of IRF5. In European-derived individuals, an IRF5 haplotype was associated with increased IRF5, IFNalpha and IFN-inducible chemokine expression. Identifying individuals genetically predisposed to increased IFN-inducible gene and chemokine expression may allow early detection of risk for SLE.

PubMed Disclaimer

Figures

Figure 1
Figure 1
Interferon regulatory factor 5 (IRF5) gene structure and haplotypic architecture (A) Translated exons are shown as boxes. Single nucleotide polymorphisms (SNPs) used in the analysis have been encoded as: rs4728142 (SNP 1), rs752637 (SNP 2), rs3807306 (SNP 3), rs11761199 (SNP 4), rs6975315 (SNP 5), rs7808907 (SNP 6), rs1874328 (SNP 7), rs6970960 (SNP 8), rs6951628 (SNP 9), rs13242262 (SNP 10), rs1727172 (SNP 11), rs10488630 (SNP 12), rs10488631 (SNP 13) and rs2280714 (SNP 14). (B) Linkage disequilibrium (LD) r2 chart summarises the LD pattern in European (CEU), Han Chinese + Japanese (CHB+JPT) and Yoruba Nigerian (YRI) individuals as a plot. Darker grey represents regions of high pairwise r2 and white represents regions of low pairwise r2. The numbers in the boxes are the pairwise r2 values. TagSNPs are noted by asterisks. (C) The haplotypes across IRF5 constructed from 58 unrelated CEU individuals. The haplotypes are numbered on the left of each haplotype and haplotype frequencies are shown to the right of each haplotype. The SNP numbers across the top of the haplotypes correspond to those in the gene diagram above. The grey-boxed haplotype is the risk haplotype, defined by the risk alleles of SNPs 10, 13 and 14. The black-boxed haplotype is the non-risk haplotype.
Figure 2
Figure 2
Association of interferon regulatory factor 5 (IRF5) single nucleotide polymorphisms (SNPs) with increased IRF5 expression in three samples. IRF5 expression in European, Chinese/Japanese and Yoruba Nigerian individuals with or without risk alleles (homozygotes only) of (A) rs13242262 (SNP 10) and (B) rs2280714 (SNP 14). All p values withstand the Bonferroni correction method. SNP 14 is a proxy for the known functional SNP rs10954213, the polyadenylation variant site.
Figure 3
Figure 3
Mean mRNA expression (±SEM) of interferon regulatory factor 5 (IRF5) and interferon α (IFNα), and mean IFN or CMK scores (±SEM) of (A) individuals of European background (CEU) with or without the systemic lupus erythematosus (SLE)-associated risk allele of single nucleotide polymorphism (SNP) 13 (rs10488631) or (B) CEU individuals with the risk haplotype (H4, black) or the non-risk haplotype (H1, white). The risk haplotype is defined by the risk alleles of SNPs 10, 13 and 14 which are all located in the 3′ downstream region. All haplotypes, including haplotype 4 (H4, AAGGCTTACA) were previously deduced using Haplotyper 1.0 and are shown in figure 1C. p Values shown are those which remained significant after application of the Bonferroni correction.
Figure 4
Figure 4
Increased relative expression of interferon-inducible genes, but not housekeeping genes, was seen in lymphoblastoid cells (LCLs) after interferon α (IFNα) stimulation. Relative expression of genes in LCLs incubated with IFNα was measured based on values of RFLPO, a non-IFN-inducible housekeeping gene and compared with expression of cells incubated with IFNα plus recombinant B18R protein, an established inhibitor of IFN activation. (A) Relative expression of GAPDH, a non-IFN-inducible gene, after stimulation of cells with IFNα. (B) The relative expression of each IFN-inducible gene (ISG15, OAS1, OASL or MX-1), with or without incubation with IFNα, was combined from all seven cell lines. A summed total representing IFN score 1 is also presented in (B). Data points were connected by lines to illustrate the gene activation of a given gene. In both panels, data are expressed as mean ± SD (SD is not shown in (B) due to overlap between data sets). Each condition was done in duplicate and results shown were one of the two representative experiments. *p<0.05 (IFN score 1, p=0.0002; OASL, p=0.006; MX-1, p=0.03); †p<0.1 (ISG15, p=0.09; OAS1, p=0.06).
See this image and copyright information in PMC

Similar articles

See all similar articles

Cited by

See all "Cited by" articles

References

    1. Crow MK, Kirou KA. Interferon-alpha in systemic lupus erythematosus. Curr Opin Rheumatol. 2004;16:541–7. - PubMed
    1. Pascual V, Farkas L, Banchereau J. Systemic lupus erythematosus: all roads lead to type I interferons. Curr Opin Immunol. 2006;18:676–82. - PubMed
    1. Niewold TB, Hua J, Lehman TJ, et al. High serum IFN-alpha activity is a heritable risk factor for systemic lupus erythematosus. Genes Immun. 2007;8:492–502. - PMC - PubMed
    1. Pascual V, Banchereau J, Palucka AK. The central role of dendritic cells and interferon-alpha in SLE. Curr Opin Rheumatol. 2003;15:548–56. - PubMed
    1. Rönnblom L, Alm GV. Systemic lupus erythematosus and the type I interferon system. Arthritis Res Ther. 2003;5:68–75. - PMC - PubMed

Publication types