Rozzo S J, Allard J D, Choubey D, Vyse T J, Izui S, Peltz G, Kotzin B L
Departments of Medicine and Immunology, University of Colorado Health Sciences Center, Denver, CO 80262, USA.
Immunity. 2001 Sep;15(3):435-43. doi: 10.1016/s1074-7613(01)00196-0.
The Nba2 locus is a major genetic contribution to disease susceptibility in the (NZB x NZW)F(1) mouse model of systemic lupus. We generated C57BL/6 mice congenic for this NZB locus, and these mice produced antinuclear autoantibodies characteristic of lupus. F(1) offspring of congenic and NZW mice developed high autoantibody levels and severe lupus nephritis similar to (NZB x NZW)F(1) mice. Expression profiling with oligonucleotide microarrays revealed only two differentially expressed genes, interferon-inducible genes Ifi202 and Ifi203, in congenic versus control mice, and both were within the Nba2 interval. Quantitative PCR localized increased Ifi202 expression to splenic B cells and non-T/non-B cells. These results, together with analyses of promoter region polymorphisms, strain distribution of expression, and effects on cell proliferation and apoptosis, implicate Ifi202 as a candidate gene for lupus.
Nba2基因座是(NZB×NZW)F1系统性红斑狼疮小鼠模型中疾病易感性的主要遗传因素。我们培育了携带该NZB基因座的C57BL/6同源基因小鼠,这些小鼠产生了狼疮特征性的抗核自身抗体。同源基因小鼠与NZW小鼠的F1代后代产生了高水平的自身抗体和严重的狼疮性肾炎,类似于(NZB×NZW)F1小鼠。用寡核苷酸微阵列进行表达谱分析发现,在同源基因小鼠与对照小鼠中,只有两个差异表达基因,即干扰素诱导基因Ifi202和Ifi203,且二者均在Nba2区间内。定量PCR将Ifi202表达的增加定位到脾脏B细胞和非T/非B细胞。这些结果,连同对启动子区域多态性、表达的品系分布以及对细胞增殖和凋亡的影响的分析,表明Ifi202是狼疮的候选基因。