Johansson C M, Kristjánsdottir H, Gröndal G, Steinsson K, Alarcón-Riquelme M E
Department of Genetics and Pathology, Rudbeck Laboratory, Uppsala University, 751 85 Uppsala, Sweden.
Scand J Immunol. 2006 Sep;64(3):308-13. doi: 10.1111/j.1365-3083.2006.01810.x.
Systemic lupus erythematosus is a systemic autoimmune disorder of unknown aetiology but is most likely caused by an interaction between several genetic factors and the environment. In a previously published genome scan we presented linkage to a marker on chromosome 4p13 in Icelandic families. Fine mapping of the region has been performed using 10 multicase families from Iceland and the maximum two-point LOD score was given by marker D4S2974 (Z = 3.57, alpha = 1). Multipoint analyses of the markers in the region suggest a putative disease gene to be located between markers D4S405 and D4S2381. The maximum multipoint LOD score (Z = 3.76) was given for marker D4S2974 in combination with the novel repeat GT4C2. A family-specific haplotype was segregating with the disease in each of eight families although a founder haplotype could not be identified. Analysis of recombination events in the patients delimited the susceptibility locus to approximately 3 cM. The susceptibility locus identified probably contains a mutation that has been enriched in the Icelandic population but is less common in other populations. We also show that this region is not identical to a susceptibility locus for SLE located on 4p16 where we detect no linkage.
系统性红斑狼疮是一种病因不明的全身性自身免疫性疾病,但很可能是由多种遗传因素与环境之间的相互作用引起的。在之前发表的一项全基因组扫描中,我们报告了冰岛家族中与4号染色体p13上一个标记的连锁关系。已使用来自冰岛的10个多病例家族对该区域进行了精细定位,标记D4S2974给出了最大两点对数优势分数(Z = 3.57,α = 1)。对该区域标记的多点分析表明,一个假定的疾病基因位于标记D4S405和D4S2381之间。标记D4S2974与新型重复序列GT4C2组合给出了最大多点对数优势分数(Z = 3.76)。尽管无法确定奠基者单倍型,但在八个家族中的每一个家族中,一种家族特异性单倍型都与疾病共分离。对患者重组事件的分析将易感基因座限定在约3厘摩的范围内。所确定的易感基因座可能包含一个在冰岛人群中富集但在其他人群中不太常见的突变。我们还表明,该区域与位于4p16上的系统性红斑狼疮易感基因座不同,在那里我们未检测到连锁关系。