Department of Pathogenomics, Ehime University Graduate School of Medicine, Toon, Ehime, Japan.
Pathol Int. 2010 Jun;60(6):430-7. doi: 10.1111/j.1440-1827.2010.02537.x.
A cumulative effect of the susceptibility genes with polymorphic alleles may be responsible for rheumatoid arthritis (RA). The objective of this study was to clarify whether susceptibility to RA is under the control of common allelic loci between two different RA models induced by extrinsic and intrinsic factors, collagen-induced arthritis (CIA) in DBA/1 mice and arthritis in MRL/Mp (MRL) mice associated with the Fas deficient mutant gene, Fas(lpr), respectively. CIA was examined in mice of parental DBA/1 and MRL, (MRL x DBA/1) F1 and (MRL x DBA/1) F2 progenies. In genome-wide screening of the severity in the F2 using microsatellite markers, significant linkage was observed on chromosomes 5 and 17 at map position of D5Mit259 and H-2, respectively, associated with DBA/1 alleles, while there was no loci associated with arthritis of MRL-Fas(lpr) mice previously identified. In a quantitative trait locus (QTL) analysis, the locus on chromosome 5 showed the highest peak at map position 35 cM (LOD score 6.0). This study may indicate that the arthritis induced by extrinsic and intrinsic factors is under the control of a different combination of susceptibility genes with common and different alleles, possibly simulating the genetic heterogeneity of RA.
遗传易感性基因的多态性等位基因的累积效应可能与类风湿关节炎(RA)有关。本研究的目的是阐明 RA 是否由两种不同的 RA 模型(由外源性和内源性因素引起的胶原诱导性关节炎(CIA)和与 Fas 缺失突变基因 Fas(lpr)相关的 MRL/Mp(MRL)小鼠关节炎)的共同等位基因座控制。在 DBA/1 小鼠和 Fas(lpr)突变基因相关的 MRL/Mp(MRL)小鼠的 CIA 模型中,观察到了两种不同的关节炎模型。在使用微卫星标记对 F2 严重程度进行全基因组筛选时,在与 DBA/1 等位基因相关的染色体 5 和 17 上的 D5Mit259 和 H-2 位置观察到显著的连锁,而与先前鉴定的 MRL-Fas(lpr)小鼠关节炎无关的基因座。在数量性状基因座(QTL)分析中,染色体 5 上的基因座在 35cM 处(LOD 评分 6.0)显示出最高峰值。本研究可能表明,外源性和内源性因素引起的关节炎受共同和不同等位基因的不同组合的易感性基因控制,可能模拟了 RA 的遗传异质性。