Delépine M, Pociot F, Habita C, Hashimoto L, Froguel P, Rotter J, Cambon-Thomsen A, Deschamps I, Djoulah S, Weissenbach J, Nerup J, Lathrop M, Julier C
Wellcome Trust Centre for Human Genetics, Oxford, United Kingdom.
Am J Hum Genet. 1997 Jan;60(1):174-87.
Linkage studies have led to the identification of several chromosome regions that may contain susceptibility loci to type I diabetes (IDDM), in addition to the HLA and INS loci. These include two on chromosome 6q, denoted IDDM5 and IDDM8, that are not linked to HLA. In a previous study, we noticed that the evidence for linkage to IDDM susceptibility around the HLA locus extended over a total distance of 100 cM, which suggested to us that another susceptibility locus could reside near HLA. We developed a statistical method to test this hypothesis in a panel of 523 multiplex families from France, the United States, and Denmark (a total of 667 affected sib pairs, 536 with both parents genotyped), and here present evidence (P = .00003) of a susceptibility locus for IDDM located 32 cM from HLA in males but not linked to HLA in females and distinct from IDDM5 and IDDM8. A new statistical method to test for the presence of a second susceptibility locus linked to a known first susceptibility locus (here HLA) is presented. In addition, we analyzed our current family panel with markers for IDDM5 and IDDM8 on chromosome 6 and found suggestions of linkage for both of these loci (P = .002 and .004, respectively, on the complete family panel). When cumulated with previously published results, with overlapping families removed, the affected-sib-pair tests had a significance of P = .0001 for IDDM5 and P = .00004 for IDDM8.
连锁研究已确定了几个除HLA和INS基因座外可能包含1型糖尿病(IDDM)易感基因座的染色体区域。其中包括位于6号染色体q上的两个区域,分别标记为IDDM5和IDDM8,它们与HLA不连锁。在之前的一项研究中,我们注意到HLA基因座周围与IDDM易感性连锁的证据延伸了100厘摩的总距离,这使我们推测另一个易感基因座可能位于HLA附近。我们开发了一种统计方法,在来自法国、美国和丹麦的523个多重家庭样本(总共667对患病同胞对,其中536对父母均进行了基因分型)中检验这一假设,在此展示了男性中存在一个距HLA 32厘摩的IDDM易感基因座的证据(P = 0.00003),但该基因座在女性中与HLA不连锁,且与IDDM5和IDDM8不同。本文提出了一种新的统计方法,用于检验与已知的第一个易感基因座(此处为HLA)连锁的第二个易感基因座的存在。此外,我们用6号染色体上IDDM5和IDDM8的标记分析了我们当前的家庭样本,发现这两个基因座均有连锁迹象(在完整家庭样本中,P分别为0.002和0.004)。当与之前发表的结果累计,并去除重叠家庭后,患病同胞对检验中IDDM5的显著性为P = 0.0001,IDDM8的显著性为P = 0.00004。