Genetic control of spontaneous arthritis in a four-way advanced intercross line

PLoS One. 2013 Oct 11;8(10):e75611. doi: 10.1371/journal.pone.0075611. eCollection 2013.

Abstract

Identifying the genetic basis of complex diseases, such as rheumatoid arthritis, remains a challenge that requires experimental models to reduce the genetic and environmental variability. Numerous loci for arthritis have been identified in induced animal models; however, few spontaneous models have been genetically studied. Therefore, we generated a four-way advanced intercross line (AIL) from four inbred strains, including BXD2/TyJ which spontaneously develops autoimmune arthritis. A genome-wide scan for spontaneous arthritis was performed in a cohort of 366 mice of the fourth generation (G4) of this cross. Five loci contributing to clinical phenotypes were identified in chromosomes 3, 7, 13, 18, and X. Three of the loci found in this study, confirm previously identified loci; whereas two of them are novel loci. Interesting candidate genes for the loci are highlighted. This study provides a genetic overview of spontaneous arthritis in mice and aids to solve the genetic etiology of rheumatoid arthritis and to gain a better understanding of the disease.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Arthritis, Experimental / genetics*
  • Arthritis, Experimental / immunology
  • Arthritis, Experimental / pathology
  • Arthritis, Rheumatoid / genetics*
  • Arthritis, Rheumatoid / immunology
  • Arthritis, Rheumatoid / pathology
  • Autoimmunity / genetics*
  • Chromosome Mapping
  • Chromosomes, Mammalian
  • Crosses, Genetic
  • Female
  • Gene Expression Regulation / immunology*
  • Genotype
  • Male
  • Mice
  • Mice, Transgenic
  • Molecular Sequence Annotation
  • Phenotype
  • Quantitative Trait Loci*

Grants and funding

This research was supported by grants from DFG (DFG IB 24/6-1,DFG GRK 1727/1), Excellence Cluster Inflammation at Interfaces (DFG EXC 306/1-2), and BMBF (IMPAM 01EC1008F). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.