Klitz W, Stephens J C, Grote M, Carrington M
Department of Integrative Biology, University of California, Berkeley 94720, USA.
Am J Hum Genet. 1995 Dec;57(6):1436-44.
Disequilibrium between genetic markers is expected to decline monotonically with recombinational map distance. We present evidence from the HLA class II region that seems to violate this principle. Pairwise disequilibrium values were calculated from six loci ranging in physical separation from 15 kb to 550 kb. The histocompatibility loci DRB1, DQA1, and DQB1, located on the distal end of the class II region, behave as a single evolutionary unit within which extremely high linkage disequilibrium exists. Lower but still significant levels of disequilibrium are present between these loci and DPB1, located at the proximal edge of the HLA complex. The peptide-transporter loci TAP1 and TAP2, located in the intervening region, reveal no disequilibrium with each other and low or negligible disequilibrium with the flanking loci. The action of two genetic process is required to account for this phenomenon: a recombinational hotspot operating between TAP1 and TAP2, to eliminate disequilibrium between these loci, and at the same time selection operating on particular combinations of alleles across the DR-DP region, to create disequilibrium in the favored haplotypes. The forces producing the patterns of disequilibrium observed here have implications for the mapping of train loci and disease genes: markers of TAP1, for example, would give a false impression as to the influence of DPB1 on a trait known to be associated with DQB1.
遗传标记之间的不平衡预计会随着重组图谱距离单调下降。我们提供了来自HLA II类区域的证据,似乎违反了这一原则。成对不平衡值是根据六个物理距离从15 kb到550 kb的位点计算得出的。位于II类区域远端的组织相容性位点DRB1、DQA1和DQB1表现为一个单一的进化单元,其中存在极高的连锁不平衡。这些位点与位于HLA复合体近端边缘的DPB1之间存在较低但仍显著的不平衡水平。位于中间区域的肽转运体位点TAP1和TAP2彼此之间没有显示出不平衡,与侧翼位点的不平衡程度较低或可忽略不计。需要两个遗传过程的作用来解释这一现象:一个重组热点在TAP1和TAP2之间起作用,以消除这些位点之间的不平衡,同时选择作用于DR-DP区域等位基因的特定组合,以在有利单倍型中产生不平衡。这里观察到的产生不平衡模式的力量对性状位点和疾病基因的定位有影响:例如,TAP1的标记会给人一种关于DPB1对已知与DQB1相关性状影响的错误印象。