Jorde L B, Watkins W S, Carlson M, Groden J, Albertsen H, Thliveris A, Leppert M
Department of Human Genetics, University of Utah Health Sciences Center, Salt Lake City 84112.
Am J Hum Genet. 1994 May;54(5):884-98.
To test the reliability of linkage-disequilibrium analysis for gene mapping, we compared physical distance and linkage disequilibrium among seven polymorphisms in the adenomatous polyposis coli (APC) region on chromosome 5. Three of them lie within the APC gene, and two lie within the nearby MCC (mutated in colon cancer) gene. One polymorphism lies between the two genes, and one is likely to be 5' of MCC. Five of these polymorphisms are newly reported. All polymorphisms were typed in the CEPH kindreds, yielding 179-205 unrelated two-locus haplotypes. Linkage disequilibrium between each pair of polymorphisms is highly correlated with physical distance in this 550-kb region (correlation coefficient -.80, P < .006). This result is replicated in both the Utah and non-Utah CEPH kindreds. There is a tendency for greater disequilibrium among pairs of polymorphisms located within the same gene than among other pairs of polymorphisms. Trigenic, quadrigenic, three-locus, and four-locus disequilibrium measures were also estimated, but these measures revealed much less disequilibrium than did the two-locus disequilibrium measures. A review of 19 published disequilibrium studies, including this one, shows that linkage disequilibrium nearly always correlates significantly with physical distance in genomic regions > 50-60 kb but that it does not do so in smaller genomic regions. We show that this agrees with theoretical predictions. This finding helps to resolve controversies regarding the use of disequilibrium for inferring gene order. Disequilibrium mapping is unlikely to predict gene order correctly in regions < 50-60 kb in size but can often be applied successfully in regions of 50-500 kb or so in size. It is convenient that this is the range in which other mapping techniques, including chromosome walking and linkage mapping, become difficult.
为了测试连锁不平衡分析用于基因定位的可靠性,我们比较了5号染色体上腺瘤性息肉病基因(APC)区域内7个多态性位点之间的物理距离和连锁不平衡情况。其中3个位于APC基因内,2个位于附近的结肠癌突变基因(MCC)内。1个多态性位点位于这两个基因之间,另一个可能在MCC基因的5'端。这些多态性位点中有5个是新报道的。所有多态性位点都在CEPH家系中进行了分型,得到了179 - 205个非亲缘双位点单倍型。在这个550 kb的区域内,每对多态性位点之间的连锁不平衡与物理距离高度相关(相关系数 -0.80,P < 0.006)。这一结果在犹他州和非犹他州的CEPH家系中均得到了验证。位于同一基因内的多态性位点对之间的不平衡趋势比其他多态性位点对之间的不平衡趋势更大。还估计了三基因、四基因、三位点和四位点的不平衡度量,但这些度量所显示的不平衡比双位点不平衡度量要少得多。对包括本研究在内的19项已发表的不平衡研究进行综述表明,在大于50 - 60 kb的基因组区域中,连锁不平衡几乎总是与物理距离显著相关,但在较小的基因组区域中并非如此。我们表明这与理论预测相符。这一发现有助于解决关于使用不平衡来推断基因顺序的争议。不平衡定位在大小小于50 - 60 kb的区域不太可能正确预测基因顺序,但在大小约为50 - 500 kb的区域通常可以成功应用。方便的是,这正是其他定位技术(包括染色体步移和连锁定位)变得困难的范围。