Gregersen P K, Kao H, Nunez-Roldan A, Hurley C K, Karr R W, Silver J
Department of Rheumatic Diseases, New York University Medical Center 10003.
J Immunol. 1988 Aug 15;141(4):1365-8.
We have analyzed DNA sequence polymorphisms of DQ alpha and DQ beta chains from three haplotypes from the DRw52 family: DR5 DQw1 (FPA, GM3106), DRw6 DQw1 (CB6B, 10w9060), and DRw6 DQw3 (AMALA, 10w9064). The results indicate that the DR5 DQw1 and DRw6 DQw1 haplotypes have arisen by recombination between the DR beta 1 and DQ alpha loci. This contrasts with our previous analysis of DR4 DQ"Wa", DR3 DQ"Wa", and DR7 DQw3 haplotypes, all of which appear to have arisen by virtue of recombination between DQ alpha and DQ beta. Thus, there appear to be at least two different sites where recombination has occurred within the DR and DQ subregions. These differing patterns of recombination were interpreted in the context of the three major family groups of class II haplotypes, the DRw53, DRw52, and DR1/2 haplotype families. The data indicate that haplotypes from these family groups tend to undergo recombination at different locations. We propose that these differences in site of recombination are a reflection of differences in the molecular organization of the haplotypes belonging to each family group.
我们分析了来自DRw52家族三种单倍型的DQα和DQβ链的DNA序列多态性:DR5 DQw1(FPA,GM3106)、DRw6 DQw1(CB6B,10w9060)和DRw6 DQw3(AMALA,10w9064)。结果表明,DR5 DQw1和DRw6 DQw1单倍型是由DRβ1和DQα基因座之间的重组产生的。这与我们之前对DR4 DQ“Wa”、DR3 DQ“Wa”和DR7 DQw3单倍型的分析形成对比,所有这些单倍型似乎都是由DQα和DQβ之间的重组产生的。因此,在DR和DQ亚区域内似乎至少有两个不同的重组位点。这些不同的重组模式在II类单倍型的三个主要家族组,即DRw53、DRw52和DR1/2单倍型家族的背景下进行了解释。数据表明,来自这些家族组的单倍型倾向于在不同位置发生重组。我们提出,重组位点的这些差异反映了属于每个家族组的单倍型分子组织的差异。