Miano M G, Jacobson S G, Carothers A, Hanson I, Teague P, Lovell J, Cideciyan A V, Haider N, Stone E M, Sheffield V C, Wright A F
MRC Human Genetics Unit, Western General Hospital, Edinburgh, UK.
Am J Hum Genet. 2000 Nov;67(5):1348-51. doi: 10.1016/S0002-9297(07)62966-8. Epub 2000 Sep 27.
There is much interest in use of identity-by-descent (IBD) methods to map genes, both in Mendelian and in complex disorders. Homozygosity mapping provides a rapid means of mapping autosomal recessive genes in consanguineous families by identifying chromosomal regions that show homozygous IBD segments in pooled samples. In this report, we point out some potential pitfalls that arose during the course of homozygosity mapping of the enhanced S-cone syndrome gene, resulting from (1) unexpected allelic heterogeneity, so that the region containing the disease locus was missed as a result of pooling; (2) identification of a homozygous IBD region unrelated to the disease locus; and (3) the potential for inflation of LOD scores as a result of underestimation of the extent of inbreeding, which Broman and Weber suggest may be quite common.
通过血缘同一性(IBD)方法来定位基因,无论是在孟德尔疾病还是复杂疾病中,都备受关注。纯合性定位通过识别在混合样本中显示纯合IBD片段的染色体区域,为在近亲家庭中定位常染色体隐性基因提供了一种快速方法。在本报告中,我们指出了在增强型S-锥体综合征基因的纯合性定位过程中出现的一些潜在陷阱,这些陷阱源于:(1)意外的等位基因异质性,以至于由于混合而遗漏了包含疾病位点的区域;(2)识别出与疾病位点无关的纯合IBD区域;以及(3)由于低估近亲繁殖程度而导致LOD评分膨胀的可能性,Broman和Weber认为这种情况可能相当普遍。