Fine Mapping, Gene Content, Comparative Sequencing, and Expression Analyses Support Ctla4 and Nramp1 as Candidates for Idd5.1 and Idd5.2 in the Nonobese Diabetic Mouse 1

At least two loci that determine susceptibility to type 1 diabetes in the NOD mouse have been mapped to chromosome 1, Idd5.1 (insulin-dependent diabetes 5.1) and Idd5.2. In this study, using a series of novel NOD.B10 congenic strains, Idd5.1 has been defined to a 2.1-Mb region containing only four genes, Ctla4, Icos, Als2cr19, and Nrp2 (neuropilin-2), thereby excluding a major candidate gene, Cd28. Genomic sequence comparison of the two functional candidate genes, Ctla4 and Icos, from the B6 (resistant at Idd5.1) and the NOD (susceptible at Idd5.1) strains revealed 62 single nucleotide polymorphisms (SNPs), only two of which were in coding regions. One of these coding SNPs, base 77 of Ctla4 exon 2, is a synonymous SNP and has been correlated previously with type 1 diabetes susceptibility and differential expression of a CTLA-4 isoform. Additional expression studies in this work support the hypothesis that this SNP in exon 2 is the genetic variation causing the biological effects of Idd5.1. Analysis of additional congenic strains has also localized Idd5.2 to a small region (1.52 Mb) of chromosome 1, but in contrast to the Idd5.1 interval, Idd5.2 contains at least 45 genes. Notably, the Idd5.2 region still includes the functionally polymorphic Nramp1 gene. Future experiments to test the identity of Idd5.1 and Idd5.2 as Ctla4 and Nramp1, respectively, can now be justified using approaches to specifically alter or mimic the candidate causative SNPs.

[1]  Eric S. Lander,et al.  The mosaic structure of variation in the laboratory mouse genome , 2002, Nature.

[2]  T. Kitsukawa,et al.  Targeting of both mouse neuropilin-1 and neuropilin-2 genes severely impairs developmental yolk sac and embryonic angiogenesis , 2002, Proceedings of the National Academy of Sciences of the United States of America.

[3]  V. Kuchroo,et al.  The Diabetes Susceptibility Locus Idd5.1 on Mouse Chromosome 1 Regulates ICOS Expression and Modulates Murine Experimental Autoimmune Encephalomyelitis 1 , 2004, The Journal of Immunology.

[4]  M. Lefranc,et al.  Human Ig superfamily CTLA‐4 gene: chromosomal localization and identity of protein sequence between murine and human CTLA‐4 cytoplasmic domains , 1988, European journal of immunology.

[5]  H. Garchon,et al.  Further mapping of the Idd5.1 locus for autoimmune diabetes in NOD mice. , 2001, Diabetes.

[6]  W. Lee,et al.  Functional and ontogenetic analysis of murine CD45Rhi and CD45Rlo CD4+ T cells. , 1990, Journal of immunology.

[7]  J. Bluestone,et al.  Loss of CTLA-4 leads to massive lymphoproliferation and fatal multiorgan tissue destruction, revealing a critical negative regulatory role of CTLA-4. , 1995, Immunity.

[8]  E. Puré,et al.  Changes in CD45 isoform expression accompany antigen-induced murine T-cell activation. , 1989, Proceedings of the National Academy of Sciences of the United States of America.

[9]  P. Gros,et al.  Natural resistance to infection with intracellular parasites: molecular genetics identifies Nramp1 as the Bcg/Ity/Lsh locus , 1995, Journal of leukocyte biology.

[10]  N. Sarvetnick,et al.  IL-10 is necessary and sufficient for autoimmune diabetes in conjunction with NOD MHC homozygosity , 1996, The Journal of experimental medicine.

[11]  A. Theofilopoulos Genes and genetics of autoimmunity , 1999 .

[12]  Luc J. Smink,et al.  Association of the T-cell regulatory gene CTLA4 with susceptibility to autoimmune disease , 2003, Nature.

[13]  L. Sandkuijl,et al.  A Gly15Arg mutation in the interleukin-10 gene reduces secretion of interleukin-10 in Crohn disease. , 2003, Scandinavian journal of gastroenterology.

[14]  P. Lyons,et al.  Localising quantitative trait loci in the NOD mouse model of type 1 diabetes. , 1999, Current directions in autoimmunity.

[15]  Pascale Jeannin,et al.  A soluble form of CTLA‐4 generated by alternative splicing is expressed by nonstimulated human T cells , 1999, European journal of immunology.

[16]  J. Todd,et al.  The derivation of highly germline-competent embryonic stem cells containing NOD-derived genome. , 2003, Diabetes.

[17]  S. Grinstein,et al.  Iron chelators modulate the fusogenic properties of Salmonella-containing phagosomes , 2003, Proceedings of the National Academy of Sciences of the United States of America.

[18]  G. Freeman,et al.  ICOS is critical for CD40-mediated antibody class switching , 2001, Nature.

[19]  L. Overbergh,et al.  Quantification of murine cytokine mRNAs using real time quantitative reverse transcriptase PCR. , 1999, Cytokine.

[20]  G. Eisenbarth,et al.  Insulin autoantibodies are associated with islet inflammation but not always related to diabetes progression in NOD congenic mice. , 2003, Diabetes.

[21]  Olivier Hermine,et al.  A neuronal receptor, neuropilin-1, is essential for the initiation of the primary immune response , 2002, Nature Immunology.

[22]  Richard J. Mural,et al.  Genome-wide single-nucleotide polymorphism analysis defines haplotype patterns in mouse , 2003, Proceedings of the National Academy of Sciences of the United States of America.

[23]  J. Todd,et al.  NOD Idd5 locus controls insulitis and diabetes and overlaps the orthologous CTLA4/IDDM12 and NRAMP1 loci in humans. , 2000, Diabetes.

[24]  M. Oaks,et al.  Cutting Edge: A Soluble Form of CTLA-4 in Patients with Autoimmune Thyroid Disease , 2000, The Journal of Immunology.

[25]  A. Suzuki,et al.  Regulated protein–protein interaction between aPKC and PAR‐3 plays an essential role in the polarization of epithelial cells , 2002, Genes to cells : devoted to molecular & cellular mechanisms.

[26]  T. Petes,et al.  Meiotic recombination hot spots and cold spots , 2001, Nature Reviews Genetics.

[27]  P. Blair,et al.  ICOS Costimulation Requires IL-2 and Can Be Prevented by CTLA-4 Engagement1 , 2001, The Journal of Immunology.

[28]  H. Himmelbauer,et al.  Molecular cloning and characterization of murine ICOS and identification of B7h as ICOS ligand , 2000, European journal of immunology.