Lonjou C, Collins A, Ajioka R S, Jorde L B, Kushner J P, Morton N E
Human Genetics, University of Southampton, Princess Anne Hospital, Southampton SO16 54A, United Kingdom.
Proc Natl Acad Sci U S A. 1998 Sep 15;95(19):11366-70. doi: 10.1073/pnas.95.19.11366.
Recombination acts on the genetic map, not on the physical map. On the other hand, the physical map is usually more accurate. Choice of the genetic or physical map for positional cloning by allelic association depends on the goodness of fit of data to each map under an established model. Huntington disease illustrates the usual case in which the greater reliability of physical data outweighs recombinational heterogeneity. Hemochromatosis represents an exceptional case in which unrecognized recombinational heterogeneity retarded positional cloning for a decade. The Malecot model performs well for major genes, but no approach assuming either equilibrium or disequilibrium has been validated for oligogenes contributing to common disease. In this case of greatest interest, the power of allelic association relative to linkage is less clear than for major genes.
重组作用于遗传图谱,而非物理图谱。另一方面,物理图谱通常更为精确。通过等位基因关联进行定位克隆时,选择遗传图谱还是物理图谱取决于既定模型下数据与每种图谱的拟合优度。亨廷顿舞蹈症说明了通常的情况,即物理数据更高的可靠性超过了重组异质性。血色素沉着症则代表了一个特殊情况,未被识别的重组异质性使定位克隆推迟了十年。马勒科特模型对主基因效果良好,但对于导致常见疾病的寡基因,尚未有任何假设平衡或不平衡的方法得到验证。在这个最受关注的案例中,相对于连锁分析,等位基因关联的效力不如主基因那么明确。