Johannesson M, Hultqvist M, Holmdahl R
Medical Inflammation Research, Lund University, Sweden.
Curr Top Microbiol Immunol. 2006;305:259-76. doi: 10.1007/3-540-29714-6_13.
It has so far been difficult to identify genes behind polygenic autoimmune diseases such as rheumatoid arthritis (RA), multiple sclerosis (MS), and type I diabetes (T1D). With proper animal models, some of the complexity behind these diseases can be reduced. The use of linkage analysis and positional cloning of genes in animal models for RA resulted in the identification of one of the genes regulating severity of arthritis in rats and mice, the Ncf1 gene. The Ncf1 gene encodes for the Ncf1 protein that is involved in production of free oxygen radicals through the NADPH oxidase complex, which opens up a new pathway for therapeutic treatment of inflammatory diseases. In most cases, however, a quantitative trait locus (QTL) is the sum effect of several genes within and outside the QTL, which make positional cloning difficult. Here we will discuss the possibilities and difficulties of gene identification in animal models of autoimmune disorders.
迄今为止,要确定类风湿性关节炎(RA)、多发性硬化症(MS)和I型糖尿病(T1D)等多基因自身免疫性疾病背后的基因一直很困难。借助合适的动物模型,这些疾病背后的一些复杂性可以得到简化。在RA动物模型中使用基因连锁分析和定位克隆,结果鉴定出了调控大鼠和小鼠关节炎严重程度的其中一个基因,即Ncf1基因。Ncf1基因编码Ncf1蛋白,该蛋白通过NADPH氧化酶复合物参与游离氧自由基的产生,这为炎症性疾病的治疗开辟了一条新途径。然而,在大多数情况下,数量性状基因座(QTL)是该QTL内外几个基因的综合效应,这使得定位克隆变得困难。在此,我们将讨论在自身免疫性疾病动物模型中进行基因鉴定的可能性和困难。