Rubinstein P, Ginsberg-Fellner F, Falk C
Am J Hum Genet. 1981 Nov;33(6):865-82.
Three different published sets of HLA-typed families of juvenile diabetes mellitus (JDM) patients have been analyzed. There was no significant genetic heterogeneity between them according to the criterion of Morton, and the total material was analyzed on the assumption of a single recessive (JDM-P) gene with incomplete penetrance. The analysis, carried out with the NYLIP program modified to account for penetrance less than 1 and for selection bias, yields highly significant lod scores for linkage between HLA and JDM-P, with a maximum value of 7.40 at theta = .05 +/- .03. The segregation of HLA and GLO in five affected sib pairs, in which one of the sibs carries an HLA/GLO recombinant, places JDM-P closer to HLA than the GLO locus: four of these five pairs are HLA-identical and GLO-different, in agreement with the conclusions of the formal linkage analysis. The data from these three independent sets of families are therefore consistent with our earlier claim that JDM is inherited as a recessive trait closely linked to HLA with reduced penetrance, and its analysis does not require more complicated genetic models.
对已发表的三组不同的青少年糖尿病(JDM)患者的HLA分型家系进行了分析。根据莫顿标准,它们之间不存在显著的遗传异质性,并且在单个隐性(JDM-P)基因且外显率不完全的假设下对全部资料进行了分析。使用经过修改的NYLIP程序进行分析,该程序考虑了外显率小于1以及选择偏倚的情况,得出HLA与JDM-P之间连锁的lod分数高度显著,在θ = 0.05±0.03时最大值为7.40。在五个患病同胞对中HLA和GLO的分离情况,其中一个同胞携带HLA/GLO重组体,表明JDM-P比GLO基因座更靠近HLA:这五对中的四对HLA相同而GLO不同,这与形式连锁分析的结论一致。因此,来自这三组独立家系的数据与我们早期的观点一致,即JDM作为一种隐性性状遗传,与HLA紧密连锁且外显率降低,并且对其分析不需要更复杂的遗传模型。