Holmdahl Rikard
Medical Inflammation Research, Lund University, Lund, Sweden.
Nat Clin Pract Rheumatol. 2007 Feb;3(2):104-11. doi: 10.1038/ncprheum0400.
Complex traits, including inflammatory rheumatic diseases, have important genetic features, but most of the responsible genes have not been conclusively identified. Genetic analysis of inbred animal models and comparative genetics--the comparison of genes between different species--might help to identify the crucial genes and to investigate more directly the biology involved. Genome-wide linkage analysis of particular genes can be assessed by genetic segregation studies, whereas disease pathways can be delineated by the use of congenic strains. To clone disease genes, the traits need to be transformed so that they are inherited in a more Mendelian manner: achieving this pattern requires isolation of the locus on a genetic background that allows high penetrance by minimization of the size of congenic fragments, genetic manipulations without associated artifacts, or identification of highly penetrant mutations by phenotypic selection. Although almost one hundred quantitative trait loci for arthritis have been identified, only a few genes have so far been positionally cloned. In this Review we highlight the possibilities of using animal models to identify genes associated with complex diseases like arthritis, illustrated with available findings for genes such as those encoding major histocompatibility complex class II, neutrophil cytosolic factor 1 (Ncf1/p47(phox)) and ZAP70.
包括炎性风湿性疾病在内的复杂性状具有重要的遗传特征,但大多数相关基因尚未得到最终确认。近交动物模型的遗传分析以及比较遗传学(即不同物种间基因的比较)可能有助于识别关键基因,并更直接地研究其中涉及的生物学机制。特定基因的全基因组连锁分析可通过遗传分离研究进行评估,而疾病途径可通过使用同类系来描绘。为了克隆疾病基因,需要对性状进行转化,使其以更符合孟德尔遗传的方式遗传:要实现这种模式,需要在一个遗传背景上分离该基因座,通过最小化同类系片段的大小、进行无相关假象的遗传操作或通过表型选择识别高外显率突变来实现高外显率。尽管目前已鉴定出近百个与关节炎相关的数量性状基因座,但到目前为止只有少数基因通过定位克隆得到。在本综述中,我们重点介绍了利用动物模型识别与关节炎等复杂疾病相关基因的可能性,并以编码主要组织相容性复合体II类、中性粒细胞胞质因子1(Ncf1/p47(phox))和ZAP70等基因的现有研究结果为例进行说明。