Yang H T, Jirholt J, Svensson L, Sundvall M, Jansson L, Pettersson U, Holmdahl R
Beijer Laboratory, Department of Genetics and Pathology, Unit of Medical Genetics, Biomedical Center, Uppsala University, Sweden.
J Immunol. 1999 Sep 1;163(5):2916-21.
The susceptibility to collagen-induced arthritis in the highly susceptible DBA/1 mouse has earlier been shown to be partly controlled by the MHC class II gene Aq. To identify susceptibility loci outside of MHC, we have made crosses between DBA/1 and the less susceptible B10.Q strain, both expressing the MHC class II gene Aq. Analysis of 224 F2 intercross mice with 170 microsatellite markers in a genome-wide scan suggested 4 quantitative trait loci controlling arthritis susceptibility located on chromosomes 6, 7, 8, and 10. The locus on chromosome 6 (Cia6), which was associated with arthritis onset, yielded a logarithm of odds score of 4.7 in the F2 intercross experiment and was reproduced in serial backcross experiments. Surprisingly, the DBA/1 allele had a recessive effect leading to a delay in arthritis onset. The suggestive loci on chromosomes 7 and 10 were associated with arthritis severity rather than onset, and another suggestive locus on chromosome 8 was most closely associated with arthritis incidence. The loci on chromosomes 7, 8, and 10 all appeared to contain disease-promoting alleles derived from the DBA/1 strain. Interestingly, most of the identified loci were situated in chromosomal regions that are homologous to regions in the rat genome containing susceptibility genes for arthritis; the mouse Cia6 locus is homologous with the rat Cia3, Pia5, Pia2, and Aia3; the locus on chromosome 7 (Cia7) is homologous with the rat Cia2; and the locus on chromosome 10 (Cia8) is homologous with the rat Cia4.
早前研究表明,高度易感的DBA/1小鼠对胶原诱导性关节炎的易感性部分受MHC II类基因Aq控制。为了确定MHC之外的易感基因座,我们将DBA/1与易感性较低的B10.Q品系进行杂交,这两个品系均表达MHC II类基因Aq。在全基因组扫描中,对224只F2代杂交小鼠和170个微卫星标记进行分析,结果表明有4个数量性状基因座控制关节炎易感性,分别位于6号、7号、8号和10号染色体上。6号染色体上的基因座(Cia6)与关节炎发病相关,在F2代杂交实验中其优势对数得分为4.7,并在系列回交实验中得到重现。令人惊讶的是,DBA/1等位基因具有隐性效应,导致关节炎发病延迟。7号和10号染色体上的提示性基因座与关节炎严重程度而非发病相关,8号染色体上的另一个提示性基因座与关节炎发病率关系最为密切。7号、8号和10号染色体上的基因座似乎都含有源自DBA/1品系的促病等位基因。有趣的是,大多数已确定的基因座位于与大鼠基因组中包含关节炎易感基因的区域同源的染色体区域;小鼠的Cia6基因座与大鼠的Cia3、Pia5、Pia2和Aia3同源;7号染色体上的基因座(Cia7)与大鼠的Cia2同源;10号染色体上的基因座(Cia8)与大鼠的Cia4同源。