Sex Differences in Correlation with Gene Expression Levels between Ifi200 Family Genes and Four Sets of Immune Disease-Relevant Genes

Author:

Cao Yanhong12ORCID,Wang Lishi23,Wang Cong-Yi4,Ye Jicheng3,Wang Ying1,Li Tiantian1,Garcia-Godoy Franklin5,Sun Dianjun1,Gu Weikuan26ORCID,Postlethwaite Arnold E.67ORCID

Affiliation:

1. Center for Endemic Disease Control, Center for Disease Control and Prevention, Harbin Medical University, Harbin 150081, China

2. Departments of Orthopaedic Surgery-Campbell Clinic and Pathology, University of Tennessee Health Science Center (UTHSC), Memphis, TN 38163, USA

3. Department of Basic Medical Research, Inner Mongolia Medical University, Jinshan New Investment and Development Zones, Hohhort, Inner Mongolia 010110, China

4. The Center for Biomedical Research, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, 1095 Jiefang Ave, Wuhan 430030, China

5. Bioscience Research Center, College of Dentistry, University of Tennessee Health Science Center (UTHSC), 875 Union Avenue, Memphis, TN 38163, USA

6. Research Service, Memphis VA Medical Center, 1030 Jefferson Avenue, Memphis, TN 38104, USA

7. Division of Connective Tissue Diseases, Department of Medicine, University of Tennessee Health Science Center (UTHSC), Memphis, TN 38163, USA

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.

Funder

Department of Veterans Affairs

Publisher

Hindawi Limited

Subject

Immunology,General Medicine,Immunology and Allergy

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