Abstract

Background The HIN-200 family genes in humans have been linked to several autoimmune diseases—particularly to systemic lupus erythematosus (SLE) and rheumatoid arthritis (RA). Recently, its human counterpart gene cluster, the Ifi200 family in mice, has been linked to spontaneous arthritis disease (SAD). However, many immune-mediated diseases (including RA and SLE) show gender difference. Understanding whether or not and how these genes play a role in sex difference in immune-mediated diseases is essential for diagnosis/treatment. Methods This study takes advantage of the whole genome gene expression profiles of recombinant inbred (RI) strain populations from female and male mice to analyze potential sex differences in a variety of genes in disease pathways. Expression levels and regulatory QTL of Ifi200 family genes between female and male mice were first examined in a large mouse population, including RI strains derived from C57BL/6J, DBA/2J (BXD), and classic inbred strains. Sex similarities and differences were then analyzed for correlations with gene expression levels between genes in the Ifi200 family and four selected gene sets: known immune Ifi200 pathway-related genes, lupus-relevant genes, osteoarthritis- (OA-) and RA-relevant genes, and sex hormone-related genes. Results The expression level of Ifi202b showed the most sex difference in correlation with known immune-related genes (the P value for Ifi202b is 0.0004). Ifi202b also showed gender difference in correlation with selected sex hormone genes, with a P value of 0.0243. When comparing coexpression levels between Ifi200 genes and lupus-relevant genes, Ifi203 and Ifi205 showed significant sex difference (P values: 0.0303 and 0.002, resp.). Furthermore, several key genes (e.g., Csf1r, Ifnb1, IL-20, IL-22, IL-24, Jhdm1d, Csf1r, Ifnb1, IL-20, IL-22, IL-24, and Tgfb2 that regulate sex differences in immune diseases) were discovered. Conclusions Different genes in the Ifi200 family play different roles in sex difference among dissimilar pathways of these four gene groups.

Highlights

  • The HIN-200 family genes in humans have been linked to several autoimmune diseases— to systemic lupus erythematosus (SLE) and rheumatoid arthritis (RA)

  • IFI16 is in the same paralogue with pyrin and is an HIN domain family member 1 (PYHIN1 or IFIX), myeloid cell nuclear differentiation antigen (MNDA), and absent in melanoma 2 (AIM2) on human chromosome 1 as a human HIN-200 gene cluster

  • Interferon-inducible protein-10 (IP-10) was found to be linked to RA, it is not located in the human HIN200 cluster [11, 12]

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Summary

Introduction

The HIN-200 family genes in humans have been linked to several autoimmune diseases— to systemic lupus erythematosus (SLE) and rheumatoid arthritis (RA). Ifi200 genes, including the human HIN-200 gene cluster and its mouse counterpart, the interferon inducible200 (Ifi200) family, have been linked to several autoimmune diseases [1,2,3,4,5]. These genes have been linked to SLE. Interferon-inducible protein-10 (IP-10) was found to be linked to RA, it is not located in the human HIN200 cluster [11, 12] These findings suggest that it is possible that Ifi200 family genes may play an important role in the development of arthritis

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